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Monochaetum vulcanicum

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 UUID644048c743eb7951259754
Scientific name Monochaetum vulcanicum
Authority Cogn.
First published in A.L.P.de Candolle & A.C.P.de Candolle, Monogr. Phan. 7: 401 (1891)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Monochaetum carazoi Cogn. Monogr. Phan. 7: 481. 1891; et ex Th. Dur.
Monochaetum vulcanicum f. costaricense Gleason Amer. J. Bot. 16: 591 (1929)
Monochaetum vulcanicum f. glandulosum Gleason Amer. J. Bot. 16: 591 (1929)
Monochaetum vulcanicum f. typicum Gleason Amer. J. Bot. 16: 591 (1929)

Common names Top

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Language Common/alternative name
Chinese 火山单缨木

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001081117
Tropicos 20302710
KEW urn:lsid:ipni.org:names:573738-1
The Plant List tro-20302710
Open Tree Of Life 225162
Observations.org 339610
NCBI Taxonomy 1160581
IPNI 163769-2
iNaturalist 123577
GBIF 6634590
EOL 5441456
Elurikkus 578840
CMAUP NPO27072

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)!
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Title Authors Publication Released IDs
A new ursane triterpene from Monochaetum vulcanicum that inhibits DNA polymerase beta lyase. Chaturvedula VS, Gao Z, Jones SH, Feng X, Hecht SM, Kingston DG J Nat Prod 01-May-2004
doi:10.1021/NP030531B
PMID:15165161

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/NP030531B
(1S,2R,4aS,6aS,6bR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 5316084 Click to see 472.70 unknown https://doi.org/10.1021/NP030531B
10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 73218938 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1C)C)C(=O)O 602.80 unknown https://doi.org/10.1021/NP030531B
10-acetyloxy-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 73803814 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)C2C1C)C)C(=O)O 514.70 unknown https://doi.org/10.1021/NP030531B
3-(p-Coumaroyl)ursolic acid 24203733 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1C)C)C(=O)O 602.80 unknown https://doi.org/10.1021/NP030531B
3-O-Acetylcorosolic acid 21578960 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)C2C1C)C)C(=O)O 514.70 unknown https://doi.org/10.1021/NP030531B
Colosolic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP030531B
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP030531B
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1021/NP030531B
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1021/NP030531B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Methost-8-enol 6452640 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3CCC4C(C)CCCC(C)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5R,6R)-2-[[(3S,8R,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163035648 Click to see 590.90 unknown https://doi.org/10.1021/NP030531B
2-[[17-(5-Ethyl-6-methylheptan-2-yl)-10,13,14-trimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75072132 Click to see CCC(CCC(C)C1CCC2(C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)C(C)C 590.90 unknown https://doi.org/10.1021/NP030531B
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/10.1021/NP030531B
Chondrillast-7-enol 5283639 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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/10.1021/NP030531B
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP030531B
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid amides / 2-heteroaryl carboxamides
2-[[(5Z)-2-amino-5-[3-[(4,5-dibromo-1H-pyrrole-2-carbonyl)amino]propylidene]imidazol-4-yl]amino]ethanesulfonic acid 10436427 Click to see 512.18 unknown via CMAUP database
4,5-Dibromo-1h-pyrrole-2-carboxamide 14056555 Click to see C1=C(NC(=C1Br)Br)C(=O)N 267.91 unknown via CMAUP database
Cyclooroidin 10739060 Click to see 389.05 unknown via CMAUP database
N-[5-[(E)-3-aminoprop-1-enyl]-1H-imidazol-2-yl]-4,5-dibromo-1H-pyrrole-2-carboxamide 23425087 Click to see 389.05 unknown via CMAUP database
Oroidin 6312649 Click to see 389.05 unknown via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine 1123 Click to see 125.15 unknown via CMAUP database
> Organohalogen compounds / Aryl halides / Aryl bromides
4,5-dibromo-1H-pyrrole-2-carbonitrile 324098 Click to see 249.89 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles / Substituted imidazoles / Aminoimidazoles
5-[(E)-3-aminoprop-1-enyl]-1H-imidazol-2-amine 10820593 Click to see 138.17 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones
2,2,6,6-Tetramethyl-4-piperidone 13220 Click to see CC1(CC(=O)CC(N1)(C)C)C 155.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Dihydropyridines
2,4,6,6-Tetramethyl-3(6H)-pyridinone 21775038 Click to see CC1=CC(N=C(C1=O)C)(C)C 151.21 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives
methyl 4,5-dibromo-1H-pyrrole-2-carboxylate 324097 Click to see 282.92 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives / Pyrrole carboxylic acids / Pyrrole 2-carboxylic acids
4,5-Dibromo-2-Pyrrolic Acid 161830 Click to see C1=C(NC(=C1Br)Br)C(=O)O 268.89 unknown via CMAUP database

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