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Tripterygium regelii

Tripterygium regelii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64405b3a2f03b991191603
Scientific name Tripterygium regelii
Authority Sprague & Takeda
First published in Bull. Misc. Inform. Kew 1912: 223 (1912)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Tripterygium regelii var. occidentale T.Yamaz. J. Jap. Bot. 68: 365 (1993)
Tripterygium regelii f. hypoleucum (Hayashi) H.Hara
Tripterygium wilfordii var. regelii (Sprague & Takeda) Makino

Common names Top

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Language Common/alternative name
Persian تریپتریگیوم رگلی
Japanese クロヅル
Chinese 东北雷公藤

Subspecies (abbr. subsp./ssp.) Top

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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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001292786
Tropicos 6600884
KEW urn:lsid:ipni.org:names:162907-1
The Plant List tro-6600884
Open Tree Of Life 483028
NCBI Taxonomy 123485
IPNI 162907-1
iNaturalist 499126
GBIF 7265500
Freebase /m/0gkz124
EPPO TPTRE
USDA GRIN 40504
Wikipedia Tripterygium_regelii
CMAUP NPO2348

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
Phytocompounds targeting epigenetic modulations: an assessment in cancer Khan A, Khan A, Khan MA, Malik Z, Massey S, Parveen R, Mustafa S, Shamsi A, Husain SA Front Pharmacol 26-Mar-2024
PMCID:PMC11002180
doi:10.3389/fphar.2023.1273993
PMID:38596245
Sequence-Structure Analysis Unlocking the Potential Functional Application of the Local 3D Motifs of Plant-Derived Diterpene Synthases Zhao Y, Liang Y, Luo G, Li Y, Han X, Wen M Biomolecules 17-Jan-2024
PMCID:PMC10813164
doi:10.3390/biom14010120
PMID:38254720
Natural products modulate NLRP3 in ulcerative colitis Xue JC, Yuan S, Hou XT, Meng H, Liu BH, Cheng WW, Zhao M, Li HB, Guo XF, Di C, Li MJ, Zhang QG Front Pharmacol 02-Oct-2023
PMCID:PMC10577194
doi:10.3389/fphar.2023.1265825
PMID:37849728
Adaptation to pollination by fungus gnats underlies the evolution of pollination syndrome in the genus Euonymus Mochizuki K, Okamoto T, Chen KH, Wang CN, Evans M, Kramer AT, Kawakita A Ann Bot 23-Aug-2023
PMCID:PMC10583214
doi:10.1093/aob/mcad081
PMID:37610846
Drug target of natural products and COVID-19: how far has science progressed? Raman K, Rajagopal K, Ramesh B, Nallasivan PK, Raja MK, Jupudi S, Byran G, Khan SL, Bin Emran T Ann Med Surg (Lond) 19-Apr-2023
PMCID:PMC10289732
doi:10.1097/MS9.0000000000000703
PMID:37363478
Emerging drugs targeting cellular redox homeostasis to eliminate acute myeloid leukemia stem cells Costa RG, Silva SL, Dias IR, Oliveira MD, Rodrigues AC, Dias RB, Bezerra DP Redox Biol 02-Apr-2023
PMCID:PMC10119960
doi:10.1016/j.redox.2023.102692
PMID:37031536
Traditional Chinese medicine in thyroid-associated orbitopathy Hai YP, Lee AC, Chen K, Kahaly GJ J Endocrinol Invest 12-Feb-2023
PMCID:PMC10185651
doi:10.1007/s40618-023-02024-4
PMID:36781592
Plant-derived compounds for treating autosomal dominant polycystic kidney disease Zhang J, Chen J, Xu J, Xue C, Mao Z Front Nephrol 03-Feb-2023
PMCID:PMC10479581
doi:10.3389/fneph.2023.1071441
PMID:37675342
Site-specific nanomodulator capable of modulation apoptosis for enhanced colorectal cancer chemo-photothermal therapy Wang S, Zhou L, Tian H, Li B, Su M, Li Q, Nice EC, Huang C, Shao J, He T J Nanobiotechnology 20-Jan-2023
PMCID:PMC9863191
doi:10.1186/s12951-023-01779-5
PMID:36670444
The complete chloroplast genome of Tripterygium wilfordii Hook. f. (Celastraceae) Zhong Y, Zhang J, Bao Z Mitochondrial DNA B Resour 23-Sep-2022
PMCID:PMC9518234
doi:10.1080/23802359.2022.2119103
PMID:36188665
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Potential medicinal plants involved in inhibiting 3CLpro activity: A practical alternate approach to combating COVID-19 Yang F, Jiang XL, Tariq A, Sadia S, Ahmed Z, Sardans J, Aleem M, Ullah R, Bussmann RW J Integr Med 09-Aug-2022
PMCID:PMC9359926
doi:10.1016/j.joim.2022.08.001
PMID:35985974
Nanoscale Technologies in the Fight against COVID-19: From Innovative Nanomaterials to Computer-Aided Discovery of Potential Antiviral Plant-Derived Drugs Iraci N, Corsaro C, Giofrè SV, Neri G, Mezzasalma AM, Vacalebre M, Speciale A, Saija A, Cimino F, Fazio E Biomolecules 30-Jul-2022
PMCID:PMC9405735
doi:10.3390/biom12081060
PMID:36008954
雷公藤制剂治疗IgA肾病的作用机制 N/A Zhong Nan Da Xue Xue Bao Yi Xue Ban 28-May-2022
PMCID:PMC10929912
doi:10.11817/j.issn.1672-7347.2022.210410
PMID:35753727
Endoplasmic Reticulum Stress in Liver Diseases Ajoolabady A, Kaplowitz N, Lebeaupin C, Kroemer G, Kaufman RJ, Malhi H, Ren J Hepatology 24-May-2022
PMCID:PMC9637239
doi:10.1002/hep.32562
PMID:35524448

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenanthrenes and derivatives
Dihydrocelastrol 10411574 Click to see CC1=C2CC=C3C(C2=CC(=C1O)O)(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 452.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3S,3aS,5aR,5bR,7S,7aR,11aR,11bR,13aS,13bS)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-ol 163195203 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.1248/CPB.37.2836
3-(2-Hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-ol 4603262 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.1248/CPB.37.2836
Zeorin 159931 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.1248/CPB.37.2836
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(5,7-Dibenzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl) pyridine-2-carboxylate 163083827 Click to see CC1(C2CC(C3(C(CCC(C3(C2OC(=O)C4=CC=CC=N4)O1)(C)O)OC(=O)C5=CC=CC=C5)C)OC(=O)C6=CC=CC=C6)C 599.70 unknown https://doi.org/10.1248/CPB.35.4683
[(1S,2S,5S,6S,7S,9R,12R)-5,7-dibenzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] pyridine-2-carboxylate 163083828 Click to see CC1(C2CC(C3(C(CCC(C3(C2OC(=O)C4=CC=CC=N4)O1)(C)O)OC(=O)C5=CC=CC=C5)C)OC(=O)C6=CC=CC=C6)C 599.70 unknown https://doi.org/10.1248/CPB.35.4683
Regelidine 13968328 Click to see CC1(C2CC(C3(C(CCC(C3(C2OC(=O)C4=CN=CC=C4)O1)(C)O)OC(=O)C5=CC=CC=C5)C)OC(=O)C6=CC=CC=C6)C 599.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,5S,6R,9R,11R,14R,15R,19S,21S)-11-hydroxy-2,5,6,10,10,14,21-heptamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 44575701 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)C 454.70 unknown https://doi.org/10.1248/CPB.35.2125
(1S,2R,6R,11S,14R,15R)-11-hydroxy-2,5,6,10,10,14,21-heptamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 122130063 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)C 454.70 unknown via CMAUP database
10-Hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 4274774 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
https://doi.org/10.1016/J.FCT.2010.11.044
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
3-Epikatonic acid 10434225 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)00007-8
Celastrol 122724 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown https://doi.org/10.1016/J.FCT.2010.11.044
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
https://doi.org/10.1016/S0031-9422(00)00007-8
CID 21672631 21672631 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)O)C(=O)OC 484.70 unknown https://doi.org/10.1248/CPB.35.2125
Desoxoglabrolide 5257561 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)C 454.70 unknown https://doi.org/10.1248/CPB.35.2125
methyl (1R,4aR,6bR,10S,12aR)-4,10-dihydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-2-carboxylate 5320901 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C)O)C(=O)OC 486.70 unknown via CMAUP database
methyl (1R,4aR,6bR,9R,12aR)-4-acetyloxy-9-(hydroxymethyl)-1,4a,6a,6b,9,12a-hexamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-2-carboxylate 5320898 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)C)OC(=O)C)C(=O)OC 542.70 unknown via CMAUP database
methyl (2S,4aR,6bR,10S,12aR)-4,10-dihydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylate 5320902 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)OC)C)C)C)C 486.70 unknown via CMAUP database
methyl (2S,4aR,6bR,12aR)-4-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylate 5320899 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)OC)C)C)C)C 484.70 unknown via CMAUP database
Methyl 4-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-2-carboxylate 14466907 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)O)C(=O)OC 484.70 unknown https://doi.org/10.1248/CPB.35.2125
Methyl 4-hydroxy-9-(hydroxymethyl)-1,4a,6a,6b,9,12a-hexamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-2-carboxylate 14466909 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)C)O)C(=O)OC 500.70 unknown https://doi.org/10.1248/CPB.35.2125
Oleanolic acid acetate 6708573 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)00007-8
Orthosphenic acid 20056194 Click to see CC1C23CCC4C(C2CC(C1(OC3)O)O)(CCC5(C4(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C 488.70 unknown https://doi.org/10.1016/S0031-9422(00)00007-8
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
Regelin 163808 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)O)C(=O)OC 484.70 unknown via CMAUP database
Regelin C 122391246 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)O)C(=O)OC 484.70 unknown https://doi.org/10.1248/CPB.35.2125
https://doi.org/10.1248/CPB.37.2836
https://doi.org/10.1248/CPB.35.4683
Regelinol 163809 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)C)O)C(=O)OC 500.70 unknown https://doi.org/10.1248/CPB.35.2125
https://doi.org/10.1248/CPB.37.2836
https://doi.org/10.1248/CPB.35.4683
Salaspermic acid 44593364 Click to see CC1C23CCC4C(C2CCC1(OC3)O)(CCC5(C4(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)00007-8
Triptotriterpenic acid A 21594203 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)O)C)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)00007-8
Wilforlide A 158477 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)C 454.70 unknown https://doi.org/10.1248/CPB.35.2125
https://doi.org/10.1248/CPB.37.2836
https://doi.org/10.1016/S0031-9422(00)00007-8
https://doi.org/10.1016/J.BSE.2016.07.005
Wilforlide B 174362 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)C 452.70 unknown https://doi.org/10.1016/S0031-9422(00)00007-8
https://doi.org/10.1016/J.BSE.2016.07.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
5-Hydroxy-15-(4-hydroxy-5,6-dimethylheptan-2-yl)-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-1(11)-en-10-one 162814795 Click to see CC(C)C(C)C(CC(C)C1CCC2C1(CCC3=C2C(=O)C4C5(C3(CCC(C5)O)C)O4)C)O 444.60 unknown https://doi.org/10.1248/CPB.37.2836
https://doi.org/10.1248/CPB.35.4683
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Triptophenolide 173273 Click to see CC(C)C1=C(C2=C(C=C1)C3(CCC4=C(C3CC2)COC4=O)C)O 312.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.BSE.2016.07.005
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.BSE.2016.07.005
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
{[2-Hydroxy-1,1-bis(hydroxymethyl)ethyl]ammonio}acetate 6992779 Click to see C(C(=O)[O-])[NH2+]C(CO)(CO)CO 179.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(2R,4aS,6aS,6aS,14aS,14bR)-10-hydroxy-2,4a,6a,6a,14a-pentamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 5701992 Click to see CC12CCC(CC1C3(CCC4(C(=CC=C5C4=CC(=O)C(=C5)O)C3(CC2)C)C)C)(C)C(=O)O 436.60 unknown via CMAUP database
(6aS,6bS,8aS,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-8,9,12,12a,13,14-hexahydro-7H-picen-2-one 46881919 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
3-Hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 3527193 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
3-Hydroxy-4,6b,8a,11,12b,14a-hexamethyl-7,8,8a,9,12,12a,12b,13,14,14a-decahydropicen-2(6bh)-one 162727 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127101/
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
3-[[7-(2-hydroxy-3-methoxy-3-methylbutyl)-2-(2-methylbut-3-en-2-yl)-5-(3-methylbut-2-enyl)-1H-indol-3-yl]methyl]-6-methylpiperazine-2,5-dione 142737379 Click to see CC1C(=O)NC(C(=O)N1)CC2=C(NC3=C(C=C(C=C23)CC=C(C)C)CC(C(C)(C)OC)O)C(C)(C)C=C 509.70 unknown https://doi.org/10.1248/CPB.35.2125
> Organoheterocyclic compounds / Isoquinolines and derivatives
1-(3-(6,7-Dimethoxyisoquinolin-1-yl)propyl)guanidine 10062645 Click to see COC1=C(C=C2C(=C1)C=CN=C2CCCN=C(N)N)OC 288.34 unknown via CMAUP database
Crispine B 10105261 Click to see COC1=C(C=C2C3=[N+](CCC3)C=CC2=C1)OC 230.28 unknown via CMAUP database
Crispine D 10069639 Click to see COC1=C(C=C2C(=C1)C(=CN=C2CCCN=C(N)N)CCCCN=C(N)N)OC 401.50 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(+)-Crispine A 11673094 Click to see COC1=C(C=C2C3CCCN3CCC2=C1)OC 233.31 unknown via CMAUP database
2-[3-[(1S)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]propyl]guanidine 24823534 Click to see COC1=C(C=C2C(NCCC2=C1)CCCN=C(N)N)OC 292.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[3-(6-Deoxy-alpha-L-mannopyranosyloxy)-4-hydroxyphenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one 21721958 Click to see CC1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 11377340 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)OC)O)CO)O)O)O)O)O 666.60 unknown via CMAUP database
Linariifolioside 5492485 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 652.60 unknown via CMAUP database

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