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Ophiorrhiza pumila

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe54e4eae7864113907
Scientific name Ophiorrhiza pumila
Authority Champ. ex Benth.
First published in Hooker's J. Bot. Kew Gard. Misc. 4: 169 (1852)

Ethnobotanical Use Top

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General Uses Top

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Scientific and model organism uses:
Ophiorrhiza pumila is used as a research organism in studies of monoterpene indole alkaloid (MIA) biosynthesis, notably in the camptothecin pathway, and for comparative phylogenetic analyses within Rubiaceae. It is maintained in sequence databases (e.g., GenBank/NCBI) and referenced as a genetic resource for pathway reconstruction and gene discovery.

Properties relevant to use:
The presence of a biosynthetic pathway capable of generating MIAs in O. pumila supports its use in elicitation studies, transcriptomic analyses of alkaloid metabolism, and root culture systems that model specialized metabolite production.

Standards and regulation:
No specific standards apply to the plant as a research taxon; standard scientific resource policies apply (e.g., NCBI data policies).

Synonyms Top

Scientific name Authority First published in
Ophiorrhiza humilis Y.C.Tseng Fl. Hainan. 3: 583 (1974)
Ophiorrhiza inflata Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 488 (1888)
Ophiorrhiza pumila var. inflata (Maxim.) Masam. Trans. Nat. Hist. Soc. Formosa 29: 238. 1939

Common names Top

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Language Common/alternative name
Japanese チャボイナモリ
Chinese 小蛇根草
Chinese 溪畔蛇根草
Chinese 白花蛇根草
Chinese 短小蛇根草
Chinese 琼崖蛇根草
Chinese 绿蛇根草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000257203
Tropicos 27913302
KEW urn:lsid:ipni.org:names:758576-1
The Plant List kew-140558
Open Tree Of Life 608350
NCBI Taxonomy 157934
IPNI 758576-1
iNaturalist 504870
GBIF 5340840
EOL 1102492
USDA GRIN 468242

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_016586305.1 Opu_r1.4 Scaffold Kazusa DNA Research Institute 2020-12-09 130 419.71 Mb

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
Strategies, Achievements, and Potential Challenges of Plant and Microbial Chassis in the Biosynthesis of Plant Secondary Metabolites Han T, Miao G Molecules 02-May-2024
PMCID:PMC11085123
doi:10.3390/molecules29092106
PMID:38731602
Telomere-to-telomere genome assembly of Oldenlandia diffusa Gao Y, Xu D, Hu Z DNA Res 11-Apr-2024
PMCID:PMC11041053
doi:10.1093/dnares/dsae012
PMID:38600880
Chromosome-level Alstonia scholaris genome unveils evolutionary insights into biosynthesis of monoterpenoid indole alkaloids Chen H, Sahu SK, Wang S, Liu J, Yang J, Cheng L, Chiu TY, Liu H iScience 27-Mar-2024
PMCID:PMC11033161
doi:10.1016/j.isci.2024.109599
PMID:38646178
Induction of Monoterpenoid Oxindole Alkaloids Production and Related Biosynthetic Gene Expression in Response to Signaling Molecules in Hamelia patens Plant Cultures López-Vázquez AL, Sepúlveda-García EB, Rubio-Rodríguez E, Ponce-Noyola T, Trejo-Tapia G, Barrera-Cortés J, Cerda-García-Rojas CM, Ramos-Valdivia AC Plants (Basel) 27-Mar-2024
PMCID:PMC11013434
doi:10.3390/plants13070966
PMID:38611495
The Madagascar palm genome provides new insights on the evolution of Apocynaceae specialized metabolism Cuello C, Jansen HJ, Abdallah C, Zamar Mbadinga DL, Birer Williams C, Durand M, Oudin A, Papon N, Giglioli-Guivarc'h N, Dirks RP, Jensen MK, O'Connor SE, Besseau S, Courdavault V Heliyon 14-Mar-2024
PMCID:PMC10963385
doi:10.1016/j.heliyon.2024.e28078
PMID:38533072
Enhancement of specialized metabolites using CRISPR/Cas gene editing technology in medicinal plants Das S, Kwon M, Kim JY Front Plant Sci 21-Feb-2024
PMCID:PMC10915232
doi:10.3389/fpls.2024.1279738
PMID:38450402
Genomic characterization of WRKY transcription factors related to secoiridoid biosynthesis in Gentiana macrophylla Yin Y, Fu H, Mi F, Yang Y, Wang Y, Li Z, He Y, Yue Z BMC Plant Biol 23-Jan-2024
PMCID:PMC10804491
doi:10.1186/s12870-024-04727-z
PMID:38262919
Eco-friendly approaches to phytochemical production: elicitation and beyond Jalota K, Sharma V, Agarwal C, Jindal S Nat Prod Bioprospect 10-Jan-2024
PMCID:PMC10776560
doi:10.1007/s13659-023-00419-7
PMID:38195902
High quality genomes produced from single MinION flow cells clarify polyploid and demographic histories of critically endangered Fraxinus (ash) species Fleck SJ, Tomlin C, da Silva Coelho FA, Richter M, Danielson ES, Backenstose N, Krabbenhoft T, Lindqvist C, Albert VA Commun Biol 06-Jan-2024
PMCID:PMC10771460
doi:10.1038/s42003-023-05748-4
PMID:38184717
Plant disease resistance outputs regulated by AP2/ERF transcription factor family Ma N, Sun P, Li ZY, Zhang FJ, Wang XF, You CX, Zhang CL, Zhang Z Stress Biol 02-Jan-2024
PMCID:PMC10758382
doi:10.1007/s44154-023-00140-y
PMID:38163824
Transcriptome and Metabolome Analysis of Isoquinoline Alkaloid Biosynthesis of Coptis chinensis in Different Years Min X, Zhu T, Hu X, Hou C, He J, Liu X Genes (Basel) 18-Dec-2023
PMCID:PMC10742649
doi:10.3390/genes14122232
PMID:38137054
Integrating genomic and multiomic data for Angelica sinensis provides insights into the evolution and biosynthesis of pharmaceutically bioactive compounds Li S, Chiu TY, Jin X, Cao D, Xu M, Zhu M, Zhou Q, Liu C, Zong Y, Wang S, Yu K, Zhang F, Bai M, Liu G, Liang Y, Zhang C, Simonsen HT, Zhao J, Liu B, Zhao S Commun Biol 24-Nov-2023
PMCID:PMC10674023
doi:10.1038/s42003-023-05569-5
PMID:38001348
The Rauvolfia tetraphylla genome suggests multiple distinct biosynthetic routes for yohimbane monoterpene indole alkaloids Stander EA, Lehka B, Carqueijeiro I, Cuello C, Hansson FG, Jansen HJ, Dugé De Bernonville T, Birer Williams C, Vergès V, Lezin E, Lorensen MD, Dang TT, Oudin A, Lanoue A, Durand M, Giglioli-Guivarc’h N, Janfelt C, Papon N, Dirks RP, O’connor SE, Jensen MK, Besseau S, Courdavault V Commun Biol 24-Nov-2023
PMCID:PMC10673892
doi:10.1038/s42003-023-05574-8
PMID:38001233
Genome mining of metabolic gene clusters in the Rubiaceae family Correia de Lemos SM, Paschoal AR, Guyot R, Medema M, Domingues DS Comput Struct Biotechnol J 20-Nov-2023
PMCID:PMC10698576
doi:10.1016/j.csbj.2023.11.034
PMID:38075396
A target enrichment probe set for resolving phylogenetic relationships in the coffee family, Rubiaceae Ball LD, Bedoya AM, Taylor CM, Lagomarsino LP Appl Plant Sci 17-Nov-2023
PMCID:PMC10719880
doi:10.1002/aps3.11554
PMID:38106541

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 / Camptothecins
(+-)-Camptothecin 2538 Click to see 348.40 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
https://doi.org/10.1016/S0040-4039(00)95021-4
https://doi.org/10.1016/S0040-4020(02)01196-1
(19S)-19-ethyl-19-hydroxy-8-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaene-14,18-dione 11028089 Click to see 556.50 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
https://doi.org/10.1016/S0040-4039(00)95021-4
(4S)-4-Ethyl-4-hydroxy-10-methoxy-1H-pyrano[3',4' 494163 Click to see CCC1(C2=C(COC1=O)C(=O)N3CC4=CC5=C(C=CC=C5OC)N=C4C3=C2)O 378.40 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[[(19S)-19-acetyloxy-19-ethyl-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaen-8-yl]oxy]oxan-2-yl]methyl acetate 10509193 Click to see CCC1(C2=C(COC1=O)C(=O)N3CC4=CC5=C(C=CC=C5OC6C(C(C(C(O6)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)N=C4C3=C2)OC(=O)C 736.70 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
[3,4,5-Triacetyloxy-6-[(19-acetyloxy-19-ethyl-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaen-8-yl)oxy]oxan-2-yl]methyl acetate 85165658 Click to see 736.70 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
19-Ethyl-19-hydroxy-8-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaene-14,18-dione 14729431 Click to see 556.50 unknown https://doi.org/10.1016/S0040-4039(00)95021-4
https://doi.org/10.1016/S0040-4039(97)10404-X
9-Methoxycamptothecin 123617 Click to see 378.40 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Camptothecin 24360 Click to see 348.40 unknown https://doi.org/10.1016/S0040-4039(00)95021-4
https://doi.org/10.1093/PCP/PCG051
https://doi.org/10.1007/S002990100320
https://doi.org/10.1016/S0040-4039(01)80563-3
https://doi.org/10.1016/S0031-9422(97)00614-6
https://doi.org/10.1016/S0040-4039(97)10404-X
https://doi.org/10.1016/S0040-4020(02)01196-1
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methylanthraquinone 160817 Click to see 238.24 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1-Methyl-2,3-dihydroxyanthraquinone 11391150 Click to see 254.24 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
1,2-Dihydroxy-3-methoxy-4-methylanthracene-9,10-dione 163192670 Click to see 284.26 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
1,2-Dihydroxy-3-methylanthraquinone 429241 Click to see 254.24 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
2-Hydroxy-3-methylanthraquinone 10889963 Click to see 238.24 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-3-(hydroxymethyl)-5,5-dimethyl-4-[(E,3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 21674142 Click to see 386.40 unknown https://doi.org/10.1016/S0040-4039(00)95021-4
3-(Hydroxymethyl)-5,5-dimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73821784 Click to see 386.40 unknown https://doi.org/10.1016/S0040-4039(00)95021-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/S0031-9422(97)00614-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
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/S0040-4039(97)10404-X
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
Loganin pentaacetate 443344 Click to see 600.60 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Methyl 6-acetyloxy-7-methyl-1-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 598308 Click to see 600.60 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2R,3S,4R,5S,6R)-3,4,5-triacetyloxy-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]oxan-2-yl]methyl acetate 162847343 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C)OC(=O)C)OC(=O)C 526.50 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
[3,4,5-triacetyloxy-6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]oxan-2-yl]methyl acetate 13846830 Click to see 526.50 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[[(1R,18S,19R,20S)-19-ethenyl-14-oxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2,4,6,8,10,15-hexaen-18-yl]oxy]oxan-2-yl]methyl acetate 11227637 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CC4C5=NC6=CC=CC=C6C=C5CN4C(=O)C3=CO2)C=C)OC(=O)C)OC(=O)C)OC(=O)C 664.70 unknown https://doi.org/10.1016/S0040-4039(97)00858-7
[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[[(1S,18S,19R,20S)-19-ethenyl-14-oxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2,4,6,8,10,15-hexaen-18-yl]oxy]oxan-2-yl]methyl acetate 15343940 Click to see 664.70 unknown https://doi.org/10.1016/S0040-4039(97)00858-7
[3,4,5-Triacetyloxy-6-[(19-ethenyl-14-oxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2,4,6,8,10,15-hexaen-18-yl)oxy]oxan-2-yl]methyl acetate 72759677 Click to see 664.70 unknown https://doi.org/10.1016/S0040-4039(97)00858-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-Methyl 3-(3-(3,4-Dihydroxyphenyl)Acryloyloxy)-1,4,5-Trihydroxycyclohexanecarboxylate 46230348 Click to see 368.30 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
3-O-Caffeoylquinic acid methyl ester 6476139 Click to see 368.30 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Methyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate 73412063 Click to see 368.30 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(16R,18S,19R)-19-ethenyl-16-methoxy-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-14-one 101208613 Click to see COC1C2=C(C=C3C4=NC5=CC=CC=C5C=C4CN3C2=O)C(C(O1)OC6C(C(C(C(O6)CO)O)O)O)C=C 524.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
(16S,18S,19R)-19-ethenyl-16-methoxy-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-14-one 11168431 Click to see 524.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
(1R,18S,19R,20S)-19-ethenyl-18-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2,4,6,8,10,15-hexaen-14-one 163187593 Click to see C=CC1C2CC3C4=NC5=CC=CC=C5C=C4CN3C(=O)C2=COC1OC6C(C(C(C(O6)CO)O)O)O 496.50 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
(1R,18S,19R,20S)-19-ethenyl-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2,4,6,8,10,15-hexaen-14-one 11420564 Click to see C=CC1C2CC3C4=NC5=CC=CC=C5C=C4CN3C(=O)C2=COC1OC6C(C(C(C(O6)CO)O)O)O 496.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
18-[3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-19-vinyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2(11),4,6,8,15-pentaene-10,14-dione 14440700 Click to see 512.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
https://doi.org/10.1016/S0040-4039(97)10404-X
https://doi.org/10.1016/S0040-4039(01)80563-3
19-Ethenyl-16-methoxy-18-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-14-one 85422536 Click to see 524.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
19-Ethenyl-18-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2,4,6,8,10,15-hexaen-14-one 2989 Click to see 496.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
https://doi.org/10.1016/S0040-4039(00)95021-4
https://doi.org/10.1016/S0040-4039(97)10404-X
Deoxypumiloside 46173817 Click to see C=CC1C2CC3C4=NC5=CC=CC=C5C=C4CN3C(=O)C2=COC1OC6C(C(C(C(O6)CO)O)O)O 496.50 unknown https://doi.org/10.1016/S0040-4039(01)80563-3
https://doi.org/10.1016/S0040-4020(02)01196-1
https://doi.org/10.1016/S0040-4039(00)95021-4
Pumiloside 10346314 Click to see 512.50 unknown https://doi.org/10.1016/S0040-4039(01)80563-3
https://doi.org/10.1016/S0040-4020(02)01196-1
https://doi.org/10.1016/S0040-4039(97)10404-X
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
3-epi-Vincosamide; Isovincoside lactam; Strictosidine lactam 5015264 Click to see 498.50 unknown https://doi.org/10.1016/S0040-4020(02)01196-1
https://doi.org/10.1016/S0040-4039(97)10404-X
Strictosamide 10345799 Click to see 498.50 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
https://doi.org/10.1016/S0040-4020(02)01196-1
> Organoheterocyclic compounds / Tetrapyrroles and derivatives
Phaeophytin A 135421897 Click to see CCC1=C(C2=NC1=CC3=C(C4=C(C(C(=C5C(C(C(=CC6=NC(=C2)C(=C6C)C=C)N5)C)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C4=N3)C(=O)OC)O)C)C 871.20 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
Phaeophytin b 135410870 Click to see 885.20 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12-formyl-17,21,26-trimethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,5(26),6,8,10,12,14,16,18,20(23)-decaene-3-carboxylate 6602299 Click to see CCC1=C2C=C3C(=C4C(=O)C(C(=C5C(C(C(=N5)C=C6C(=C(C(=CC(=C1C=O)N2)N6)C=C)C)C)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C4=N3)C(=O)OC)C 885.20 unknown https://doi.org/10.1016/S0040-4039(97)10404-X
methyl 16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 5351507 Click to see 871.20 unknown https://doi.org/10.1016/S0040-4039(97)10404-X

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