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Tabernaemontana corymbosa

Tabernaemontana corymbosa - Unknown
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fee7da2db2317328196
Scientific name Tabernaemontana corymbosa
Authority Roxb. ex Wall.
First published in Edwards's Bot. Reg. 15: t. 1273 (1829)

Description Top

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Tabernaemontana corymbosa is a species of plant found in parts of Asia, including Brunei, China, Indonesia, Laos, Malaysia, Myanmar, Singapore, Thailand, and Vietnam. It is a frost tolerant plant that grows to about 2 metres and likes full sun to part shade. It has glossy green leaves and faintly sweet scented flowers that bloom continuously all year. There are a number of cultivars available, and the plant has been found to contain multiple compounds of different classes, including Iboga alkaloids and Bisindole alkaloids, many of which show antiproliferative and cytotoxic actions.

Synonyms Top

Scientific name Authority First published in
Pagiantha corymbosa (Roxb.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 12: 546 (1935)
Pagiantha peninsularis Kerr Bull. Misc. Inform. Kew 1937: 43 (1937)
Pseudixora sumatrana Miq. Fl. Ned. Ind. ii. 209 (1856).
Randia sumatrana Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 235 (1869)
Tabernaemontana baviensis Pit. Fl. Indo-Chine 3: 1156 (1933)
Tabernaemontana carinata Lutjeh. & Ooststr. Blumea 3: 104 (1938)
Tabernaemontana chinensis Merr. Philipp. J. Sci. 21: 507 (1922)
Tabernaemontana continentalis (Tsiang) P.T.Li Guihaia 6: 170 (1986)
Tabernaemontana continentalis var. pubiflora (Tsiang) P.T.Li Guihaia 6: 170 (1986)
Tabernaemontana cymulosa Miq. Fl. Ned. Ind. 2: 422 (1857)
Tabernaemontana hirta Hook.f. Fl. Brit. India 3: 646 (1882)
Tabernaemontana inaequalifolia Lutjeh. & Ooststr. Blumea 3: 103 (1938)
Tabernaemontana kwangsiensis (Tsiang) P.T.Li Guihaia 6: 171 (1986)
Tabernaemontana kweichowensis (Tsiang) P.T.Li Guihaia 6: 171 (1986)
Tabernaemontana laotica Pit. Fl. Indo-Chine 3: 1148 (1933)
Tabernaemontana peninsularis (Kerr) P.T.Li Guihaia 6: 173 (1986)
Tabernaemontana pubituba Merr. Pap. Michigan Acad. Sci. 24: 87 (1938 publ. 1939)
Tabernaemontana tsiangiana P.T.Li Guihaia 6: 171 (1986)
Tabernaemontana yunnanensis (Tsiang) P.T.Li Guihaia 6: 171 (1986)
Tabernaemontana yunnanensis var. heterosepala (Tsiang) P.T.Li Guihaia 6: 171 (1986)
Ervatamia corymbosa var. pubescens King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 449. 1908
Ervatamia pauciflora var. minor Ridl. J. Straits Branch Roy. Asiat. Soc. 86: 300. 1922
Ervatamia baviensis (Pit.) Pichon Mém. Mus. Natl. Hist. Nat. 27: 219 (1948)
Ervatamia chinensis (Merr.) Tsiang Acta Phytotax. Sin. 8: 244 (1963)
Ervatamia continentalis Tsiang Acta Phytotax. Sin. 8: 243 (1963)
Ervatamia continentalis var. pubiflora Tsiang Acta Phytotax. Sin. 8: 244 1963
Ervatamia corymbosa King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 448 (1908)
Ervatamia hirta King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 449 (1908)
Ervatamia inaequalifolia (Lutjeh. & Ooststr.) Pichon Mém. Mus. Natl. Hist. Nat. 27: 220 (1948)
Ervatamia jasminiflora Ridl. Fl. Malay Penins. 2: 342 (1923)
Ervatamia kwangsiensis Tsiang Acta Phytotax. Sin. 8: 238 (1963)
Ervatamia kweichowensis Tsiang Acta Phytotax. Sin. 8: 237 (1963)
Ervatamia laotica (Pit.) Pichon Mém. Mus. Natl. Hist. Nat. 27: 219 (1948)
Ervatamia longopedicellata Lý Feddes Repert. 96: 27 (1985)
Ervatamia pauciflora Ridl. J. Straits Branch Roy. Asiat. Soc. 86: 299 (1922)
Ervatamia phuongii Lý Feddes Repert. 91: 393 (1980)
Ervatamia tenuiflora Tsiang Acta Phytotax. Sin. 8: 241 (1963)
Ervatamia yunnanensis Tsiang Acta Phytotax. Sin. 8: 241 (1963)
Ervatamia yunnanensis var. heterosepala Tsiang Acta Phytotax. Sin. 8: 242 1963

Common names Top

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Language Common/alternative name
Indonesian rombusa
Vietnamese lài trâu tụ tán
Vietnamese lài trâu tán
Chinese 伞房狗牙花
Chinese 广西狗牙花
Chinese 中国狗牙花
Chinese 大陆狗牙花
Chinese 毛瓣狗牙花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000319805
Tropicos 1805532
KEW urn:lsid:ipni.org:names:60466167-2
The Plant List kew-200648
Open Tree Of Life 5794155
NCBI Taxonomy 1679252
IUCN Red List 34504
IPNI 82070-1
iNaturalist 344978
GBIF 3618099
Freebase /m/02y_r0c
EOL 2899687
Wikipedia Tabernaemontana_corymbosa

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Mukaiyama aldol reaction: an effective asymmetric approach to access chiral natural products and their derivatives/analogues Mushtaq A, Zahoor AF RSC Adv 08-Nov-2023
PMCID:PMC10631541
doi:10.1039/d3ra05058k
PMID:38025859
Inhibition of mitochondrial metabolism by (−)-jerantinine A: synthesis and biological studies in triple-negative breast cancer cells Gialelis TL, Wang Z, Homer JA, Yang WH, Chung T, Hu Q, Smedley CJ, Pawar NJ, Upadhyay NS, Tuveson DA, Lyons SK, Lukey MJ, Moses JE RSC Med Chem 01-Mar-2023
PMCID:PMC10131581
doi:10.1039/d3md00049d
PMID:37122543
Lead/Drug Discovery from Natural Resources Xu Z, Eichler B, Klausner EA, Duffy-Matzner J, Zheng W Molecules 28-Nov-2022
PMCID:PMC9736696
doi:10.3390/molecules27238280
PMID:36500375
Indole-Containing Natural Products 2019–2022: Isolations, Reappraisals, Syntheses, and Biological Activities Umer SM, Solangi M, Khan KM, Saleem RS Molecules 05-Nov-2022
PMCID:PMC9655573
doi:10.3390/molecules27217586
PMID:36364413
Naturally derived indole alkaloids targeting regulated cell death (RCD) for cancer therapy: from molecular mechanisms to potential therapeutic targets Qin R, You FM, Zhao Q, Xie X, Peng C, Zhan G, Han B J Hematol Oncol 14-Sep-2022
PMCID:PMC9471064
doi:10.1186/s13045-022-01350-z
PMID:36104717
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Apoferritin-Encapsulated Jerantinine A for Transferrin Receptor Targeting and Enhanced Selectivity in Breast Cancer Therapy Abuzaid H, Abdelrazig S, Ferreira L, Collins HM, Kim DH, Lim KH, Kam TS, Turyanska L, Bradshaw TD ACS Omega 13-Jun-2022
PMCID:PMC9244903
doi:10.1021/acsomega.2c00997
PMID:35785302
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
Alkaloids and Colon Cancer: Molecular Mechanisms and Therapeutic Implications for Cell Cycle Arrest Khan H, Alam W, Alsharif KF, Aschner M, Pervez S, Saso L Molecules 28-Jan-2022
PMCID:PMC8838632
doi:10.3390/molecules27030920
PMID:35164185
Molecular interactions at the colchicine binding site in tubulin: an X-ray crystallography perspective Wang J, Miller DD, Li W Drug Discov Today 08-Dec-2021
PMCID:PMC8901563
doi:10.1016/j.drudis.2021.12.001
PMID:34890803
Plant-Based Indole Alkaloids: A Comprehensive Overview from a Pharmacological Perspective Omar F, Tareq AM, Alqahtani AM, Dhama K, Sayeed MA, Emran TB, Simal-Gandara J Molecules 15-Apr-2021
PMCID:PMC8071433
doi:10.3390/molecules26082297
PMID:33921093
The Iboga Enigma: The Chemistry and Neuropharmacology of Iboga Alkaloids and Related Analogs Iyer RN, Favela D, Zhang G, Olson DE Nat Prod Rep 04-Mar-2021
PMCID:PMC7882011
doi:10.1039/d0np00033g
PMID:32794540
Major Bioactive Alkaloids and Biological Activities of Tabernaemontana Species (Apocynaceae) Naidoo CM, Naidoo Y, Dewir YH, Murthy HN, El-Hendawy S, Al-Suhaibani N Plants (Basel) 05-Feb-2021
PMCID:PMC7915066
doi:10.3390/plants10020313
PMID:33562893
Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera Mohammed AE, Abdul-Hameed ZH, Alotaibi MO, Bawakid NO, Sobahi TR, Abdel-Lateff A, Alarif WM Molecules 18-Jan-2021
PMCID:PMC7831967
doi:10.3390/molecules26020488
PMID:33477682
Validation of target proteins of down-regulated miR-221-5p in HeLa cells treated with Polyalthia longifolia leaf extract using label-free quantitative proteomics approaches Shanmugapriya, Othman N, Sasidharan S 3 Biotech 19-Aug-2020
PMCID:PMC7438391
doi:10.1007/s13205-020-02396-x
PMID:32850286

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
10-O-Methyljerantinine B 25112286 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC(=C(C=C6N3)OC)OC)C(=O)OC 412.50 unknown https://doi.org/10.1021/NP800435C
19S-hydroxy-(+)-vincadifformine 138911112 Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O 354.40 unknown https://doi.org/10.1055/S-2006-962535
Jerantinine B 25058083 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC(=C(C=C6N3)OC)O)C(=O)OC 398.50 unknown https://doi.org/10.1021/NP800435C
Jerantinine B Acetate 25058089 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC(=C(C=C6N3)OC)OC(=O)C)C(=O)OC 440.50 unknown https://doi.org/10.1021/NP800435C
Jerantinine D 25058085 Click to see CCC12CC(=C3C4(C1N(CC4)C(=O)C5C2O5)C6=CC(=C(C=C6N3)OC)O)C(=O)OC 412.40 unknown https://doi.org/10.1021/NP800435C
Jerantinine E 25058086 Click to see CCC12CCCN3C1C4(CC3)C5=CC(=C(C=C5NC4=C(C2)C(=O)OC)OC)O 384.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.01.001
https://doi.org/10.1021/NP800435C
Jerantinine F 25112180 Click to see COC1=C(C=C2C(=C1)NC3=C(CC45CCOC4CCN6C5C23CC6)C(=O)OC)O 398.50 unknown https://doi.org/10.1021/NP800435C
Methyl 12-ethyl-4-hydroxy-5-methoxy-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 74423099 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC(=C(C=C6N3)OC)O)C(=O)OC 398.50 unknown https://doi.org/10.1021/NP800435C
Methyl 12-ethyl-4-hydroxy-5-methoxy-16-oxo-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 74423101 Click to see CCC12CC(=C3C4(C1N(CC4)C(=O)C5C2O5)C6=CC(=C(C=C6N3)OC)O)C(=O)OC 412.40 unknown https://doi.org/10.1021/NP800435C
Methyl 12-ethyl-4-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 74423102 Click to see CCC12CCCN3C1C4(CC3)C5=CC(=C(C=C5NC4=C(C2)C(=O)OC)OC)O 384.50 unknown https://doi.org/10.1021/NP800435C
Methyl 15-oxa-8,19-diazahexacyclo[10.9.1.01,9.02,7.012,16.019,22]docosa-2,4,6,9-tetraene-10-carboxylate 14887298 Click to see COC(=O)C1=C2C3(CCN4C3C5(C1)CCOC5CC4)C6=CC=CC=C6N2 352.40 unknown https://doi.org/10.1055/S-2006-958020
Methyl 4-hydroxy-5-methoxy-15-oxa-8,19-diazahexacyclo[10.9.1.01,9.02,7.012,16.019,22]docosa-2,4,6,9-tetraene-10-carboxylate 162977017 Click to see COC1=C(C=C2C(=C1)NC3=C(CC45CCOC4CCN6C5C23CC6)C(=O)OC)O 398.50 unknown https://doi.org/10.1021/NP800435C
Methyl 5-methoxy-15-oxa-8,19-diazahexacyclo[10.9.1.01,9.02,7.012,16.019,22]docosa-2(7),3,5,9-tetraene-10-carboxylate 21674331 Click to see COC1=CC2=C(C=C1)C34CCN5C3C6(CCOC6CC5)CC(=C4N2)C(=O)OC 382.50 unknown https://doi.org/10.1055/S-2006-958020
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (1S,9S,10S,12R,13E,16R)-13-ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate 122179180 Click to see CC=C1CN2C3CC1C4(C2CC5(C4)C3N(C6=CC=CC=C56)C)C(=O)OC 350.50 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (2R)-2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate 6504264 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
> Alkaloids and derivatives / Ervatamia alkaloids
Ervatamine 161765 Click to see CCC1CN(CC2(C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C(=O)OC)C 354.40 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
> Alkaloids and derivatives / Ibogan-type alkaloids
(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-11-one 122179182 Click to see CCC1CC2CC3C1N(C2)CC(=O)C4=C3NC5=C4C=C(C=C5)OC 324.40 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
(1R,15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene 51055165 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1021/NP0105432
https://doi.org/10.1055/S-2006-962535
(1R,15S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene 89578867 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1055/S-2006-962535
https://doi.org/10.1016/0031-9422(91)80111-D
(1S)-1-[(1R,15R,17R,18R)-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-17-yl]ethanol 44566758 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1055/S-2006-962535
https://doi.org/10.1021/NP0105432
10-Methoxyibogamine 442108 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1055/S-2006-962535
https://doi.org/10.1016/0031-9422(91)80111-D
19-Epi-heyneanine 44566759 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1021/NP0105432
19(S)-Hydroxyibogamine 11077316 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1021/NP0105432
5-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]pyrrolidin-2-one 122179178 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CCC(=O)N6 393.50 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole, 7-ethyl-6,6a,7,8,9,10,12,13-octahydro-, [6R-(6alpha,6abeta,7beta,9alpha)]- 500053 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1021/NP0105432
https://doi.org/10.1055/S-2006-962535
Conodiparine D 101226044 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(=O)C)OC)NC9=CC=CC=C39)C 748.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
https://doi.org/10.1016/S0960-894X(98)00294-7
Conodurine B640243K102 5477056 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(03)00087-6
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1021/NP0105432
https://doi.org/10.1055/S-2006-962535
Ibogamine-18-carboxylic acid, 12-methoxy-, methyl ester 363270 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP0105432
https://doi.org/10.1055/S-2006-962535
Iboxygaine 71656190 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)O 326.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
Isovoacangine 44393473 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP0105432
Isovoacristine 10362598 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP0105432
methyl (12R,15E)-12-[(1R,15S,17S,18S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-6-yl]-15-ethylidene-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 118701524 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 616.80 unknown https://doi.org/10.3987/COM-02-9573
methyl (15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137628478 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1021/NP0105432
https://doi.org/10.1055/S-2006-962535
methyl (1R,15S,17R,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134688048 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP0105432
https://doi.org/10.1055/S-2006-962535
methyl (1S,12R,14R,15E,18S)-15-ethylidene-12-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 122179185 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(=CC)CN(C(C7(CO)C(=O)OC)CC8=C6NC9=CC=CC=C89)C 676.90 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12R,14R,18S)-15-ethylidene-12-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 162863030 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(=CC)CN(C(C7(CO)C(=O)OC)CC8=C6NC9=CC=CC=C89)C 676.90 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12R,14S,15E,18S)-12-[(1R,15S,17S,18S)-17-acetyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 163082862 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC6C7C(C8)C(=O)C)OC)NC9=CC=CC=C39)C 690.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,12R,14S,15E,18S)-12-[(1R,17S,18S)-17-acetyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 163185169 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC6C7C(C8)C(=O)C)OC)NC9=CC=CC=C39)C 690.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,12R,14S,15E,18S)-15-ethylidene-12-[(1R,15S,17S,18R)-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 11146863 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC6C7C(C8)C(C)O)OC)NC9=CC=CC=C39)C 692.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,12R,14S,15E,18S)-15-ethylidene-12-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 122179186 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)NCC7=CC)C(=O)OC 632.80 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12R,14S,15E,18S)-15-ethylidene-12-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 122179187 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 646.90 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12R,14S,15Z,18S)-12-[(1R,15S,17S,18R)-17-acetyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101226048 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC6C7C(C8)C(=O)C)OC)NC9=CC=CC=C39)C 690.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
methyl (1S,12R,14S,15Z,18S)-15-ethylidene-12-[(1R,15S,17S,18R)-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101226047 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC6C7C(C8)C(C)O)OC)NC9=CC=CC=C39)C 692.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
methyl (1S,12R,14S,18S)-15-ethylidene-12-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 162818742 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)NCC7=CC)C(=O)OC 632.80 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12R,14S,18S)-15-ethylidene-12-[(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 162999250 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 646.90 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12S,14R,15Z,18S)-12-[(1R,15S,17S,18R)-17-acetyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-6-yl]-15-ethylidene-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101199788 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)C6=C(N5)C7CC8CC(C7N(C8)CC6)C(=O)C)NC9=CC=CC=C39)C 630.80 unknown https://doi.org/10.3987/COM-02-9573
methyl (1S,15R,17R,18S)-17-ethyl-16-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 102121234 Click to see CCC1C2C3(CC(C1=O)CN2CCC4=C3NC5=CC=CC=C45)C(=O)OC 352.40 unknown https://doi.org/10.1021/NP0105432
methyl (1S,15R,17R,18S)-17-ethyl-6-[(1S,12R,14R,15E,18R)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 163071518 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 674.90 unknown https://doi.org/10.1016/S0031-9422(03)00087-6
methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101243095 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP0105432
methyl (1S,15R,17S,18S)-17-acetyl-5-[(1S,12R,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 11018099 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(=O)C)OC)NC9=CC=CC=C39)C 748.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-17-acetyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 10970987 Click to see CC(=O)C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 382.50 unknown https://doi.org/10.1021/NP0105432
methyl (1S,15R,17S,18S)-17-acetyl-7-[(1S,12R,14S,15Z,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 101226043 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=C5C(=C4)C6=C(N5)C7(CC8CC(C7N(C8)CC6)C(=O)C)C(=O)OC)OC)NC9=CC=CC=C39)C 748.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
https://doi.org/10.1016/S0960-894X(98)00294-7
methyl (1S,15R,17S,18S)-17-acetyl-7-[(1S,12S,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 163083378 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=C5C(=C4)C6=C(N5)C7(CC8CC(C7N(C8)CC6)C(=O)C)C(=O)OC)OC)NC9=CC=CC=C39)C 748.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-17-ethyl-5-[(1S,12R,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 10941586 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(=CC)CN(C(C7(CO)C(=O)OC)CC8=C6NC9=CC=CC=C89)C)O)C(=O)OC 720.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-17-ethyl-5-[(1S,12R,14S,15Z,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101226050 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(=CC)CN(C(C7(CO)C(=O)OC)CC8=C6NC9=CC=CC=C89)C)O)C(=O)OC 720.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
methyl (1S,15R,17S,18S)-17-ethyl-6-[(1S,12R,14R,15Z,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101254412 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 674.90 unknown https://doi.org/10.1016/S0031-9422(03)00087-6
methyl (1S,15R,17S,18S)-5-[(1R,12R,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 162890049 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)OC)NC9=CC=CC=C39)C 750.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-5-[(1S,12R,14R,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 162959543 Click to see CC=C1CNC2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)OC)NC9=CC=CC=C39 736.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-5-[(1S,12R,14R,15Z,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 12112928 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)OC)NC9=CC=CC=C39)C 720.90 unknown https://doi.org/10.1016/S0031-9422(03)00087-6
methyl (1S,15R,17S,18S)-5-[(1S,12R,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-hydroxy-17-[(1S)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 11050894 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)O)NC9=CC=CC=C39)C 736.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-5-[(1S,12R,14S,15Z,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101226046 Click to see CC=C1CNC2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)OC)NC9=CC=CC=C39 736.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
methyl (1S,15R,17S,18S)-5-[(1S,12R,14S,15Z,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101226042 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)OC)NC9=CC=CC=C39)C 750.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
https://doi.org/10.1016/S0960-894X(98)00294-7
methyl (1S,15R,17S,18S)-5-[(1S,12R,14S,15Z,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-hydroxy-17-[(1S)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101226049 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(C)O)O)NC9=CC=CC=C39)C 736.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
methyl (1S,15R,17S,18S)-7-[(1S,12R,14S,15Z,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 101226045 Click to see CC=C1CNC2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=C5C(=C4)C6=C(N5)C7(CC8CC(C7N(C8)CC6)C(C)O)C(=O)OC)OC)NC9=CC=CC=C39 736.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
methyl (1S,15R,17S,18S)-7-[(1S,12S,14R,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 163104808 Click to see CC=C1CNC2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=C5C(=C4)C6=C(N5)C7(CC8CC(C7N(C8)CC6)C(C)O)C(=O)OC)OC)NC9=CC=CC=C39 736.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15R,17S,18S)-7-[(1S,12S,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 162931071 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=C5C(=C4)C6=C(N5)C7(CC8CC(C7N(C8)CC6)C(C)O)C(=O)OC)OC)NC9=CC=CC=C39)C 750.90 unknown https://doi.org/10.1021/NP020326G
methyl (1S,15S,17S,18S)-17-ethyl-5-[(1S,12R,14S,15E)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134714950 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(03)00087-6
methyl (1S,17S,18S)-17-acetyl-5-[(1S,12R,14S,15E,18S)-15-ethylidene-18-(hydroxymethyl)-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 163186412 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)C4=C(C=CC5=C4NC6=C5CCN7CC8CC(C7C6(C8)C(=O)OC)C(=O)C)OC)NC9=CC=CC=C39)C 748.90 unknown https://doi.org/10.1021/NP020326G
methyl (3S,4S,10Z,11S,13S)-10-ethylidene-13-[(1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6-methoxy-1-methoxycarbonyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-7-yl]-6-oxa-8,15-diazapentacyclo[12.7.0.03,8.04,11.016,21]henicosa-1(14),16,18,20-tetraene-4-carboxylate 101229253 Click to see CC=C1CN2COCC3(C1CC(C4=C(CC32)C5=CC=CC=C5N4)C6=C(C=C7C(=C6)C8=C(N7)C9(CC1CC(C9N(C1)CC8)C(C)O)C(=O)OC)OC)C(=O)OC 748.90 unknown https://doi.org/10.1002/CHIN.200321180
methyl (3S,4S,10Z,11S,13S)-10-ethylidene-13-[(1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6-methoxy-1-methoxycarbonyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-6-oxa-8,15-diazapentacyclo[12.7.0.03,8.04,11.016,21]henicosa-1(14),16,18,20-tetraene-4-carboxylate 101229254 Click to see CC=C1CN2COCC3(C1CC(C4=C(CC32)C5=CC=CC=C5N4)C6=C(C=CC7=C6NC8=C7CCN9CC1CC(C9C8(C1)C(=O)OC)C(C)O)OC)C(=O)OC 748.90 unknown https://doi.org/10.1002/CHIN.200321180
Methyl 17-acetyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 85350620 Click to see CC(=O)C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 382.50 unknown https://doi.org/10.1021/NP0105432
Voacristine 196982 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1016/0031-9422(91)80111-D
> Alkaloids and derivatives / Macroline alkaloids
(+)-Affinisine 5281346 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO 308.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
[(1S,14R,15Z)-15-ethylidene-3-methyl-17-oxido-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol 101617548 Click to see CC=C1C[N+]2(C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO)[O-] 324.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
[(1S,14R,15Z)-15-ethylidene-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol 101286222 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO 308.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
Methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 134716706 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://doi.org/10.1055/S-2006-962535
Normacusine B 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1055/S-2006-958020
https://doi.org/10.1016/0031-9422(91)80111-D
> Alkaloids and derivatives / Plumeran-type alkaloids
10-O-Methyljerantinine A 25112287 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC(=C(C=C5N3)OC)OC)C(=O)OC 396.50 unknown https://doi.org/10.1021/NP800435C
Jerantinine A 25112179 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC(=C(C=C5N3)OC)O)C(=O)OC 382.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.01.001
https://doi.org/10.1021/NP800435C
Jerantinine A Acetate 25058087 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC(=C(C=C5N3)OC)OC(=O)C)C(=O)OC 424.50 unknown https://doi.org/10.1021/NP800435C
Jerantinine C 25058084 Click to see CCC12CC(=C3C4(C1N(CC4)C(=O)C=C2)C5=CC(=C(C=C5N3)OC)O)C(=O)OC 396.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.01.001
https://doi.org/10.1021/NP800435C
Jerantinine H 102508395 Click to see CCC12CCCN3C1C4(CC3)C5=CC(=C(C=C5N=C4C(C2)(C(=O)OC)O)OC)O 400.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.01.001
Methyl 12-ethyl-4-hydroxy-5-methoxy-15-oxo-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate 74423100 Click to see CCC12CC(=C3C4(C1N(CC4)C(=O)C=C2)C5=CC(=C(C=C5N3)OC)O)C(=O)OC 396.40 unknown https://doi.org/10.1021/NP800435C
Methyl 12-ethyl-4-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate 163053810 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC(=C(C=C5N3)OC)O)C(=O)OC 382.50 unknown https://doi.org/10.1021/NP800435C
> Alkaloids and derivatives / Quebrachamine alkaloids
Ervayunine 149353 Click to see CCC12CCC3=C(CCN(C1)CC4C2O4)C5=CC=CC=C5N3 296.40 unknown https://doi.org/10.1055/S-2006-962535
> Alkaloids and derivatives / Strychnos alkaloids
[(1R,11S,12E,17S)-14-(chloromethyl)-12-ethylidene-8-aza-14-azoniapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,8-tetraen-10-ylidene]methanolate 163191053 Click to see CC=C1C[N+]2(CCC34C2CC1C(=C[O-])C3=NC5=CC=CC=C45)CCl 340.80 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
20-Ethyl-10-hydroxy-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,12(21)-tetraen-9-one 163192653 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5N6C4=C2CC(C6=O)O 336.40 unknown https://doi.org/10.1016/S0040-4039(99)01018-7
methyl (1S,12S,14R,15Z,18S)-15-ethylidene-12-[(11S,12Z,17S)-12-ethylidene-10-formyl-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraen-4-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101184895 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)NC6=C(C7CC8C56CCN8CC7=CC)C=O)NC9=CC=CC=C39)C 628.80 unknown https://doi.org/10.1002/1522-2675(200204)85:4<1027::AID-HLCA1027>3.0.CO;2-1
> Alkaloids and derivatives / Tacaman alkaloids
(13S,15R,19R)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-one 122179181 Click to see CCC1(CC2CC(=O)N3C4=CC=CC=C4C5=C3C2N(C1)CC5)O 310.40 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
> Alkaloids and derivatives / Vallesaman alkaloids
CID 6912322 6912322 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
> Alkaloids and derivatives / Vobasan alkaloids
Dregamine 99108 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
methyl (1S,12R,14S,15E,18S)-15-ethylidene-12-[(1'S,2S,7'R,8'S,9'S)-9'-ethyl-5-methoxy-3-oxospiro[1H-indole-2,6'-3-azatricyclo[5.3.1.03,8]undecane]-6-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 122179188 Click to see CCC1CC2CC3C1N(C2)CCC34C(=O)C5=C(N4)C=C(C(=C5)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 662.90 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,12R,14S,18S)-15-ethylidene-12-[(1'S,2S,7'R,8'S,9'S)-9'-ethyl-5-methoxy-3-oxospiro[1H-indole-2,6'-3-azatricyclo[5.3.1.03,8]undecane]-6-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 163066305 Click to see CCC1CC2CC3C1N(C2)CCC34C(=O)C5=C(N4)C=C(C(=C5)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 662.90 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
methyl (1S,14R,15Z,18S)-15-ethylidene-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101281359 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 352.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
methyl (1S,14S,15S,18R)-15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 45268651 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
https://doi.org/10.1016/0031-9422(91)80111-D
methyl (1S,14S,15S)-15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 20056338 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
Vobasonidine 134691677 Click to see CC=C1CN(C2CC3=C(C(CC1C2(CO)C(=O)OC)N4C5=CC=CC=C5C6=C4C(CC7C(=CC)CN(C(C6)C7(CO)C(=O)OC)C)O)NC8=CC=CC=C38)C 750.90 unknown https://doi.org/10.1002/1522-2675(200204)85:4<1027::AID-HLCA1027>3.0.CO;2-1
> Alkaloids and derivatives / Yohimbine alkaloids
beta-Yohimbine 2866 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1055/S-2006-958020
https://doi.org/10.1016/0031-9422(91)80111-D
CID 5458418 5458418 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1055/S-2006-958020
https://doi.org/10.1016/0031-9422(91)80111-D
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1055/S-2006-958020
https://doi.org/10.1016/0031-9422(91)80111-D
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Neoandrographolide 9848024 Click to see CC1(CCCC2(C1CCC(=C)C2CCC3=CCOC3=O)C)COC4C(C(C(C(O4)CO)O)O)O 480.60 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(5Z)-2-(5-bromo-1H-indole-3-carbonyl)-5-[(6-hydroxy-1H-indol-3-yl)methylidene]-1H-imidazol-4-one 10456352 Click to see C1=CC2=C(C=C1O)NC=C2C=C3C(=O)N=C(N3)C(=O)C4=CNC5=C4C=C(C=C5)Br 449.30 unknown https://doi.org/10.1055/S-2006-962535
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles / Pyrrolocarbazoles
methyl (3aR,4S,11bR)-3-acetyl-4-ethyl-4-formyl-10-hydroxy-9-methoxy-2,3a,5,7-tetrahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylate 102508393 Click to see CCC1(CC(=C2C3(C1N(CC3)C(=O)C)C4=CC(=C(C=C4N2)OC)O)C(=O)OC)C=O 414.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.01.001
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Methuenine 6441095 Click to see CC=C1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 294.40 unknown https://doi.org/10.1016/S0031-9422(00)95123-9
methyl (Z)-3-[(3R,8'S,8'aS)-8'-ethyl-5-hydroxy-6-methoxy-2-oxospiro[1H-indole-3,1'-2,3,5,6,7,8a-hexahydroindolizine]-8'-yl]-2-hydroxyprop-2-enoate 102508394 Click to see CCC1(CCCN2C1C3(CC2)C4=CC(=C(C=C4NC3=O)OC)O)C=C(C(=O)OC)O 416.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.01.001
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Antirhine 5462421 Click to see C=CC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
> Organoheterocyclic compounds / Indolizidines
methyl (1R,12S,13R,15S,20R)-12-ethyl-5-methoxy-4-oxo-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,5,7,9-tetraene-10-carboxylate 102412090 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC(=O)C(=CC6=N3)OC)C(=O)OC 396.40 unknown https://doi.org/10.1021/NP800435C
> Organoheterocyclic compounds / Pyrroloazepines
5-Acetyl-2-hydroxy-1,9-diazapentacyclo[10.6.1.13,7.07,19.013,18]icosa-5,12(19),13,15,17-pentaen-8-one 163005575 Click to see CC(=O)C1=CC23CC(C1)C(N4C2=C(CCNC3=O)C5=CC=CC=C54)O 336.40 unknown https://doi.org/10.1016/S0040-4039(00)00250-1
Dippinine B 102021677 Click to see CC(=O)C1CC2CC3(C1NCCC4=C3N(C2O)C5=CC=CC=C45)C(=O)OC 368.40 unknown https://doi.org/10.3987/COM-01-9342
methyl (10R,12S,13S,14S,15S)-5-methoxy-15-methyl-9-oxo-16-oxa-8,18-diazahexacyclo[10.8.1.110,14.02,7.08,21.013,18]docosa-1(21),2(7),3,5-tetraene-12-carboxylate 102021678 Click to see CC1C2CC3CC4(C2N(CCC5=C4N(C3=O)C6=C5C=CC(=C6)OC)CO1)C(=O)OC 410.50 unknown https://doi.org/10.3987/COM-01-9342
methyl (12S,13S,15R,17S,19S)-19-hydroxy-13-[(1S)-1-hydroxyethyl]-4-methoxy-1,11-diazapentacyclo[13.3.1.02,7.08,18.012,17]nonadeca-2(7),3,5,8(18)-tetraene-17-carboxylate 21595540 Click to see CC(C1CC2CC3(C1NCCC4=C3N(C2O)C5=C4C=CC(=C5)OC)C(=O)OC)O 400.50 unknown https://doi.org/10.1080/10575639908048835
https://doi.org/10.3987/COM-01-9342
methyl (9S,10R,12S,13S,14S,15S)-9-hydroxy-15-methyl-16-oxa-8,18-diazahexacyclo[10.8.1.110,14.02,7.08,21.013,18]docosa-1(21),2,4,6-tetraene-12-carboxylate 15379135 Click to see CC1C2CC3CC4(C2N(CCC5=C4N(C3O)C6=CC=CC=C56)CO1)C(=O)OC 382.50 unknown https://doi.org/10.3987/COM-01-9342
https://doi.org/10.3987/COM-98-8339
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Voastrictine 101106477 Click to see CC=C1CN2CCC3(C2CC1C4=C3C5=CC=CC=C5N=C4)O 292.40 unknown https://doi.org/10.1016/S0040-4039(01)00802-4
> Organoheterocyclic compounds / Quinolizidines
(1'S,2S,5'R,7'R,8'S,9'S)-9'-ethyl-5'-hydroxy-5-methoxyspiro[1H-indole-2,6'-3-azatricyclo[5.3.1.03,8]undecane]-3-one 122179179 Click to see CCC1CC2CC3C1N(C2)CC(C34C(=O)C5=C(N4)C=CC(=C5)OC)O 342.40 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00117
Iboluteine 21589055 Click to see CCC1CC2CC3C1N(C2)CCC34C(=O)C5=C(N4)C=CC(=C5)OC 326.40 unknown https://doi.org/10.1016/0031-9422(91)80111-D
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-(2,4,6-trihydroxyphenyl)-2,3-dihydrochromen-4-one 163014014 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3O)O)O)C)C 440.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2018.04.020
https://doi.org/10.1016/S0960-894X(98)00294-7

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