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Kopsia pauciflora

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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 UUID643fe021a5031006396507
Scientific name Kopsia pauciflora
Authority Hook.f.
First published in Fl. Brit. India 3: 639 (1882)

Description Top

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Kopsia pauciflora is a tree in the Apocynaceae family, known for its few-flowered nature. It can grow up to 10 meters tall with a trunk diameter of 15 centimeters. The bark is typically grey, olive-brown, or white. Its flowers are white with hints of yellow or green, and its fruits turn black when ripe. There are two accepted varieties of this tree, one found in Borneo and the other in Thailand, Cambodia, Peninsular Malaysia, Singapore, and Sumatra. It can be found in forests at altitudes up to 700 meters. In the past, it was considered vulnerable, but it is now classified as a synonym of Kopsia pauciflora var. pauciflora, which has a wider distribution.

Synonyms Top

No known synonyms.

Common names Top

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No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Kopsia pauciflora var. mitrephora (Sleesen) D.J.Middleton Gard. Bull. Singapore 55: 66 (2003)
Kopsia pauciflora var. pauciflora Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000221382
Tropicos 1802831
KEW urn:lsid:ipni.org:names:79516-1
The Plant List kew-106346
Open Tree Of Life 717820
NCBI Taxonomy 1037435
IPNI 79516-1
iNaturalist 496742
GBIF 7317012
Freebase /m/0wqczf_
Wikipedia Kopsia_pauciflora

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
Samarium(ii) iodide-mediated reactions applied to natural product total synthesis Heravi MM, Nazari A RSC Adv 30-Mar-2022
PMCID:PMC8965710
doi:10.1039/d1ra08163b
PMID:35424959
Recent Advances in the Synthesis of β-Carboline Alkaloids Szabó T, Volk B, Milen M Molecules 27-Jan-2021
PMCID:PMC7866041
doi:10.3390/molecules26030663
PMID:33513936
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
Kinabalurine A, A New Monoterpene Alkaloid from a North Borneo<i>Kopsia</i> Toh-Seok Kam, K. Yoganathan Chen Wei Informa UK Limited 07-Jul-2007
doi:10.1080/10575639608044899
Kopsia pauciflora, I. Structure et Configuration Absolue de Nouveaux Alcaloïdes Indoliques Dimeres de Type Aspidospermane-Eburnane de la Serie Pleiomutine-Kopsoffine C. Kan-Fan, T. Sevenet, H. P. Husson, K. C. Chan American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50037A024
Paucidactine A and B, new indole alkaloids with a novel ring system containing a lactone moiety Toh-Seok Kam, K. Yoganathan, Chen Wei Elsevier BV 13-May-2003
doi:10.1016/0040-4039(96)00633-8
Alkaloids from Kopsia pauciflora Toh-Seok Kam, Lalitha Arasu, K. Yoganathan Elsevier BV 04-Apr-2003
doi:10.1016/S0031-9422(96)00496-7
Lahadinines A and B, new cyano-substituted indole alkaloids from Kopsia pauciflora Toh-Seok Kam, K. Yoganathan Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00350-6
Monoterpene Alkaloids from <i>Kopsia pauciflora</i> Toh-Seok Kam, Kanagasundaram Yoganathan, Chen Wei American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960725+
Pauciflorines A and B, novel melanin biosynthesis inhibitors from Kopsia Toh-Seok Kam, K Yoganathan, Takashi Koyano, Kanki Komiyama Elsevier BV 25-Jul-2002
doi:10.1016/0040-4039(96)01180-X

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
> Alkaloids and derivatives / Aspidofractine alkaloids
11-Methoxykopsilongine 101081554 Click to see COC1=C(C2=C(C=C1)C34CCN5C3C6(CCC5)CCC4(N2C(=O)OC)C(C6)(C(=O)OC)O)OC 472.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
https://doi.org/10.1016/S0031-9422(97)00350-6
dimethyl (1S,12R,15S,19R,21S,24S)-21-hydroxy-15-oxido-5,7-dioxa-2-aza-15-azoniaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate 163189194 Click to see COC(=O)C1(CC23CCC[N+]4(C2C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)[O-])O 472.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
dimethyl (1S,12R,19R,21S,24S)-21-hydroxy-5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate 11015920 Click to see COC(=O)C1(CC23CCCN4C2C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)O 456.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
dimethyl (1S,12R,19R,21S,24S)-24-cyano-21-hydroxy-5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate 101938443 Click to see COC(=O)C1(CC23CCCN4C2(C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)C#N)O 481.50 unknown https://doi.org/10.1016/S0031-9422(97)00350-6
dimethyl (1S,12S,19R,21S,24R)-21,24-dihydroxy-15-oxido-5,7-dioxa-2-aza-15-azoniaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate 101938446 Click to see COC(=O)C1(CC23CCC[N+]4(C2(C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)O)[O-])O 488.50 unknown https://doi.org/10.1016/S0031-9422(97)00350-6
dimethyl (1S,12S,19R,21S,24R)-21,24-dihydroxy-5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate 101938445 Click to see COC(=O)C1(CC23CCCN4C2(C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)O)O 472.50 unknown https://doi.org/10.1016/S0031-9422(97)00350-6
dimethyl (1S,9R,16R,18S,21S)-18-hydroxy-4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate 163053161 Click to see COC1=CC=CC2=C1N(C34C25CCN6C5C(CCC6)(CC3)CC4(C(=O)OC)O)C(=O)OC 442.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
dimethyl (1S,9R,16R,18S,21S)-21-cyano-18-hydroxy-4,5-dimethoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate 101938444 Click to see COC1=C(C2=C(C=C1)C34CCN5C3(C6(CCC5)CCC4(N2C(=O)OC)C(C6)(C(=O)OC)O)C#N)OC 497.50 unknown https://doi.org/10.1016/S0031-9422(97)00350-6
Dimethyl 18-hydroxy-4,5-dimethoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate 72758498 Click to see COC1=C(C2=C(C=C1)C34CCN5C3C6(CCC5)CCC4(N2C(=O)OC)C(C6)(C(=O)OC)O)OC 472.50 unknown https://doi.org/10.1016/S0031-9422(97)00350-6
Dimethyl 21-cyano-18-hydroxy-4,5-dimethoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate 72822298 Click to see COC1=C(C2=C(C=C1)C34CCN5C3(C6(CCC5)CCC4(N2C(=O)OC)C(C6)(C(=O)OC)O)C#N)OC 497.50 unknown https://doi.org/10.1016/S0031-9422(97)00350-6
Dimethyl 21-hydroxy-15-oxido-5,7-dioxa-2-aza-15-azoniaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate 163192297 Click to see COC(=O)C1(CC23CCC[N+]4(C2C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)[O-])O 472.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Kopsamine N-oxide 163184433 Click to see COC(=O)C1(CC23CCC[N+]4(C2C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4)[O-])O 472.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Kopsinine 7069830 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Kopsoffine 158148 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)C6=CC7=C(C=C6)NC89C71CCN2C1C(CCC2)(CC8)CC9C(=O)OC 616.80 unknown https://doi.org/10.1021/NP50037A024
Kopsoffinol 180723 Click to see CC(C12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)C6=CC7=C(C=C6)NC89C71CCN2C1C(CCC2)(CC8)CC9C(=O)OC)O 632.80 unknown https://doi.org/10.1021/NP50037A024
methyl (15S,16R,19R)-16,22-dihydroxy-18,21-dioxo-8,10,20-trioxa-5,17-diazaoctacyclo[15.6.3.01,16.04,15.04,22.06,14.07,11.015,19]hexacosa-6(14),7(11),12-triene-5-carboxylate 101699202 Click to see COC(=O)N1C2=C(C=CC3=C2OCO3)C45C16CCC78C4(N(CCC7)C(=O)C5OC(=O)C6(C8)O)O 470.40 unknown https://doi.org/10.1016/0040-4039(96)00633-8
methyl (15S,16S,19R)-22-hydroxy-18,21-dioxo-8,10,20-trioxa-5,17-diazaoctacyclo[15.6.3.01,16.04,15.04,22.06,14.07,11.015,19]hexacosa-6(14),7(11),12-triene-5-carboxylate 101699203 Click to see COC(=O)N1C2=C(C=CC3=C2OCO3)C45C16CCC78C4N(CCC7)C(=O)C5OC(=O)C6(C8)O 454.40 unknown https://doi.org/10.1016/0040-4039(96)00633-8
methyl (1R,9R,16R,18R,21S)-6-[(15R,17R,19S)-15-[(1R)-1-hydroxyethyl]-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-18-carboxylate 162873522 Click to see CC(C12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)C6=CC7=C(C=C6)NC89C71CCN2C1C(CCC2)(CC8)CC9C(=O)OC)O 632.80 unknown https://doi.org/10.1021/NP50037A024
methyl (1R,9R,16S,18R,21S)-6-[(15S,17R,19S)-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-18-carboxylate 132966072 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)C6=CC7=C(C=C6)NC89C71CCN2C1C(CCC2)(CC8)CC9C(=O)OC 616.80 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
https://doi.org/10.1021/NP50037A024
methyl (1S,4R,15R,16R,19S,22R)-16,22-dihydroxy-18,21-dioxo-8,10,20-trioxa-5,17-diazaoctacyclo[15.6.3.01,16.04,15.04,22.06,14.07,11.015,19]hexacosa-6(14),7(11),12-triene-5-carboxylate 163105901 Click to see COC(=O)N1C2=C(C=CC3=C2OCO3)C45C16CCC78C4(N(CCC7)C(=O)C5OC(=O)C6(C8)O)O 470.40 unknown https://doi.org/10.1016/0040-4039(96)01180-X
methyl (1S,4R,15R,16R,19S,22R)-22-hydroxy-18,21-dioxo-8,10,20-trioxa-5,17-diazaoctacyclo[15.6.3.01,16.04,15.04,22.06,14.07,11.015,19]hexacosa-6(14),7(11),12-triene-5-carboxylate 163106491 Click to see COC(=O)N1C2=C(C=CC3=C2OCO3)C45C16CCC78C4N(CCC7)C(=O)C5OC(=O)C6(C8)O 454.40 unknown https://doi.org/10.1016/0040-4039(96)01180-X
Methyl (9R,18R,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 21123851 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
> Alkaloids and derivatives / Eburnan-type alkaloids
1-(17-Hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-15-yl)ethanone 162997612 Click to see CC(=O)C12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 310.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
1-[(15S,17R,19R)-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-15-yl]ethanone 102445440 Click to see CC(=O)C12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 310.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
CID 163190001 163190001 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O.CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 592.80 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Eburnamenin-14-ol, 14,15-dihydro-, (14alpha)- 442066 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Eburnamenin-14-ol, 14,15-dihydro-, (14beta)- 619344 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Eburnamenin-14(15H)-one 92112 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Eburnamine 101699 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Eburnamonine 3195 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
Vinburnine 71203 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
dimethyl (1R,9S,16R,19R,20S)-4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate 163106747 Click to see COC1=CC=CC2=C1N(C34C25CCN6CCCC(C6C3C(=O)OC)(C5=O)CC4)C(=O)OC 440.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
dimethyl (1R,9S,16R,19R)-4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate 102445439 Click to see COC1=CC=CC2=C1N(C34C25CCN6CCCC(C6C3C(=O)OC)(C5=O)CC4)C(=O)OC 440.50 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives / Indolecarboxylic acids
dimethyl (1S,12S,21S)-21-hydroxy-24-oxo-5,7-dioxa-2,15-diazahexacyclo[17.2.2.112,15.01,12.03,11.04,8]tetracosa-3(11),4(8),9,19(23)-tetraene-2,21-dicarboxylate 10552307 Click to see COC(=O)C1(CC2=CCC13C4(CCN(C4=O)CCC2)C5=C(N3C(=O)OC)C6=C(C=C5)OCO6)O 470.50 unknown https://doi.org/10.1016/0040-4039(96)01180-X
Dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.19,12.01,9.03,8]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate 85182567 Click to see COC1=C(C2=C(C=C1)C34CCN(C3=O)CCCC5=CCC4(N2C(=O)OC)C(C5)(C(=O)OC)O)OC 486.50 unknown https://doi.org/10.1016/0040-4039(96)01180-X
Dimethyl 21-hydroxy-24-oxo-5,7-dioxa-2,15-diazahexacyclo[17.2.2.112,15.01,12.03,11.04,8]tetracosa-3(11),4(8),9,19(23)-tetraene-2,21-dicarboxylate 85182286 Click to see COC(=O)C1(CC2=CCC13C4(CCN(C4=O)CCC2)C5=C(N3C(=O)OC)C6=C(C=C5)OCO6)O 470.50 unknown https://doi.org/10.1016/0040-4039(96)01180-X
Pauciflorine B 10552945 Click to see COC1=C(C2=C(C=C1)C34CCN(C3=O)CCCC5=CCC4(N2C(=O)OC)C(C5)(C(=O)OC)O)OC 486.50 unknown https://doi.org/10.1016/0040-4039(96)01180-X
> Organoheterocyclic compounds / Piperidines
(4R,4aR,6R,7R,7aR)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 10511685 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1021/NP960725+
https://doi.org/10.1016/S0031-9422(96)00496-7
(4R,4aR,6R,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 162906172 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1021/NP960725+
(4R,4aS,6R,7R,7aR)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 162906173 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1021/NP960725+
(4R,4aS,6R,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 10749975 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
https://doi.org/10.1080/10575639608044899
https://doi.org/10.1021/NP960725+
(4R,4aS,7R,7aR)-2,4,7-trimethyl-3,4,4a,5,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-one 162938007 Click to see CC1CN(CC2C1CC(=O)C2C)C 181.27 unknown https://doi.org/10.1021/NP960725+
(4R,4aS,7R,7aR)-4,7-dimethyl-1,2,3,4,4a,5,7,7a-octahydrocyclopenta[c]pyridin-6-one 162851424 Click to see CC1CNCC2C1CC(=O)C2C 167.25 unknown https://doi.org/10.1021/NP960725+
(4R,4aS,7R,7aS)-2,4,7-trimethyl-3,4,4a,5,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-one 10773755 Click to see CC1CN(CC2C1CC(=O)C2C)C 181.27 unknown https://doi.org/10.1021/NP960725+
https://doi.org/10.1016/S0031-9422(96)00496-7
(4R,4aS,7R,7aS)-4,7-dimethyl-1,2,3,4,4a,5,7,7a-octahydrocyclopenta[c]pyridin-6-one 10820982 Click to see CC1CNCC2C1CC(=O)C2C 167.25 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
https://doi.org/10.1021/NP960725+
(4S,4aR,6R,7R,7aR)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 10702612 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
https://doi.org/10.1021/NP960725+
(4S,4aR,6R,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 133618335 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1021/NP960725+
(4S,4aR,7R,7aR)-2,4,7-trimethyl-3,4,4a,5,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-one 10678976 Click to see CC1CN(CC2C1CC(=O)C2C)C 181.27 unknown https://doi.org/10.1016/S0031-9422(96)00496-7
https://doi.org/10.1021/NP960725+
(4S,4aR,7R,7aS)-2,4,7-trimethyl-3,4,4a,5,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-one 101412085 Click to see CC1CN(CC2C1CC(=O)C2C)C 181.27 unknown https://doi.org/10.1021/NP960725+
1H-Cyclopenta(c)pyridin-6-ol, octahydro-2,4,7-trimethyl-, (4R,4aS,6R,7S,7aR)- 588297 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1021/NP960725+
4,7-Dimethyl-1,2,3,4,4a,5,7,7a-octahydrocyclopenta[c]pyridin-6-one 85279757 Click to see CC1CNCC2C1CC(=O)C2C 167.25 unknown https://doi.org/10.1021/NP960725+
Dihydrotecomanine 541693 Click to see CC1CN(CC2C1CC(=O)C2C)C 181.27 unknown https://doi.org/10.1021/NP960725+

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