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Lablab purpureus subsp. purpureus

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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
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Details Top

Internal ID UUID643fd8d93a763423741100
Scientific name Lablab purpureus subsp. purpureus
Authority (L.) Sweet
First published in Unknown

Description Top

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Common names Top

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Varieties (abbr. var.) 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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000181643
USDA Plants LAPUP3
Tropicos 13071676
INPN 710422
KEW urn:lsid:ipni.org:names:77172986-1
iNaturalist 208802
GBIF 7224611
USDA GRIN 314607
CMAUP NPO31286

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)!
Title Authors Publication Released IDs
Purification and separation of eight steroidal plant-growth regulators from Dolichos lablab seed. Takao YOKOTA, Jun BABA, Shigeki KOBA, NOBUTAKA TAKAHASHI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.48.2529
Brassinolide-related bioactive sterols in Dolichos lablab: Brassinolide, castasterone and a new analog, homodolicholide. Takao YOKOTA, Jun BABA, Nobutaka TAKAHASHI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.47.1409
Brassinolide-related new bioactive steroids from Dolichos lablab seed. Jun BABA, Takao YOKOTA, Nobutaka TAKAHASHI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.47.659
Aminopropylaminoalcohols in the seeds of Dolichos lablab K Hamana Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80180-M
Cytokinins in immature seeds of Dolichos lablab Takao Yokota, Junichi Ueda, Nobutaka Takahashi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85156-4
Medicinal foodstuffs. XII. Saponin constituents with adjuvant activity from hyacinth bean, the seeds of Dolichos lablab L. (1): Structures of lablabosides A, B, and C. Yoshikawa M, Murakami T, Komatsu H, Matsuda H Chem Pharm Bull (Tokyo) 01-May-1998
doi:10.1248/CPB.46.812
PMID:9621416
A saponin conjugated with 2,3-dihydro-2,5-dihydroxy-6-methyl-4H-pyran-4-one from Dolichos lablab. Yoshiki Y, Kim JH, Okubo K, Nagoya I, Sakabe T, Tamura N Phytochemistry 01-Jan-1995
doi:10.1016/0031-9422(94)00571-A
PMID:7766056

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 / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Laurate 8139 Click to see CCCCCCCCCCCC(=O)OC 214.34 unknown via CMAUP database
Methyl Tetradecanoate 31284 Click to see CCCCCCCCCCCCCC(=O)OC 242.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Heneicosanoic acid 16898 Click to see CCCCCCCCCCCCCCCCCCCCC(=O)O 326.60 unknown via CMAUP database
Nonadecanoic acid 12591 Click to see CCCCCCCCCCCCCCCCCCC(=O)O 298.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Tridecanoic acid 12530 Click to see CCCCCCCCCCCCC(=O)O 214.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown via CMAUP database
Undecanoic Acid 8180 Click to see CCCCCCCCCCC(=O)O 186.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
Tricosanoic acid 17085 Click to see CCCCCCCCCCCCCCCCCCCCCCC(=O)O 354.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 13909679 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown https://doi.org/10.1248/CPB.46.812
Calenduloside F 13909684 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown https://doi.org/10.1248/CPB.46.812
Chromosaponin I 74376401 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9CC(=O)C(=C(O9)C)O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1069.20 unknown https://doi.org/10.1016/0031-9422(94)00571-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
(2alpha,3alpha,5alpha,22R,23R)-Ergost-24(28)-ene-2,3,22,23-tetrol 13870428 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2CCC4C3(CC(C(C4)O)O)C)C)O)O 448.70 unknown https://doi.org/10.1271/BBB1961.48.2529
(2R,3S,17R)-17-[(2S,3R,4R)-3,4-dihydroxy-6-methyl-5-methylideneheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 101587911 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 462.70 unknown https://doi.org/10.1271/BBB1961.47.1409
https://doi.org/10.1271/BBB1961.47.659
https://doi.org/10.1271/BBB1961.48.2529
24-epi-Castasterone 13039027 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown https://doi.org/10.1271/BBB1961.47.1409
6-Deoxocastasterone 13870433 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CCC4C3(CC(C(C4)O)O)C)C)O)O 450.70 unknown https://doi.org/10.1271/BBB1961.48.2529
Castasterone 133534 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown https://doi.org/10.1271/BBB1961.48.2529
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
(4R,5S,15R)-15-[(2S,3R,4R)-3,4-dihydroxy-6-methyl-5-methylideneheptan-2-yl]-4,5-dihydroxy-2,16-dimethyl-9-oxatetracyclo[9.7.0.02,7.012,16]octadecan-8-one 101608671 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 478.70 unknown https://doi.org/10.1271/BBB1961.47.1409
https://doi.org/10.1271/BBB1961.48.2529
2-Butyl-3-methyl-Pyrazine 13390415 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 478.70 unknown https://doi.org/10.1271/BBB1961.48.2529
24-Epibrassinolide 3239 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 480.70 unknown https://doi.org/10.1271/BBB1961.47.1409
28-Homodolicholide 13517132 Click to see CC=C(C(C)C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 492.70 unknown https://doi.org/10.1271/BBB1961.48.2529
https://doi.org/10.1271/BBB1961.47.1409
Brassinolide 115196 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 480.70 unknown https://doi.org/10.1271/BBB1961.48.2529
> Nucleosides, nucleotides, and analogues / Purine nucleosides
(2S,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[[(Z)-4-hydroxy-3-methylbut-2-enyl]amino]purin-9-yl]oxolane-3,4-diol 94936831 Click to see CC(=CCNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)CO)O)O)CO 351.36 unknown https://doi.org/10.1016/0031-9422(81)85156-4
Zeatin riboside 6440982 Click to see CC(=CCNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)CO)O)O)CO 351.36 unknown https://doi.org/10.1016/0031-9422(81)85156-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Piperidine-2-carboxylate 25200477 Click to see C1CC[NH2+]C(C1)C(=O)[O-] 129.16 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
1,4-Diaminobutane 1045 Click to see C(CCN)CN 88.15 unknown https://doi.org/10.1016/0031-9422(92)80180-M
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Spermidine 1102 Click to see C(CCNCCCN)CN 145.25 unknown https://doi.org/10.1016/0031-9422(92)80180-M
Spermine 1103 Click to see C(CCNCCCN)CNCCCN 202.34 unknown https://doi.org/10.1016/0031-9422(92)80180-M
Thermospermine 194365 Click to see C(CCNCCCNCCCN)CN 202.34 unknown https://doi.org/10.1016/0031-9422(92)80180-M
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
trans-Zeatin 449093 Click to see CC(=CCNC1=NC=NC2=C1NC=N2)CO 219.24 unknown https://doi.org/10.1016/0031-9422(81)85156-4
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Phaseollidin 119268 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C 324.40 unknown via CMAUP database

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