Diosbulbisin D

Details

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Internal ID a7ff3620-337b-4cce-bdff-aaf9794f7194
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,2S,4S,5'S,6S,7S,8S,9S,12S,13R)-8-hydroxy-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-17,19-diene-6,2'-oxolane]-16-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H38O5/c1-16-26(12-11-23(2,15-28)32-26)31-22-14-21-19-6-5-17-13-18(29)7-9-24(17,3)20(19)8-10-25(21,4)27(16,22)30/h5-6,13,16,19-22,28,30H,7-12,14-15H2,1-4H3/t16-,19-,20+,21+,22+,23+,24+,25+,26+,27-/m1/s1
InChI Key SIGQBHIFPCZXLG-BHRXFIPESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O5
Molecular Weight 442.60 g/mol
Exact Mass 442.27192431 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.93
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL1079606

2D Structure

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2D Structure of Diosbulbisin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9821 98.21%
Caco-2 - 0.5441 54.41%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8336 83.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3561 35.61%
OATP1B3 inhibitior + 0.9112 91.12%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5148 51.48%
BSEP inhibitior + 0.9864 98.64%
P-glycoprotein inhibitior + 0.5729 57.29%
P-glycoprotein substrate - 0.5269 52.69%
CYP3A4 substrate + 0.7166 71.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8924 89.24%
CYP3A4 inhibition - 0.7294 72.94%
CYP2C9 inhibition - 0.9014 90.14%
CYP2C19 inhibition - 0.9338 93.38%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.8662 86.62%
CYP2C8 inhibition + 0.6064 60.64%
CYP inhibitory promiscuity - 0.8644 86.44%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.5738 57.38%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9756 97.56%
Skin irritation + 0.6756 67.56%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.7207 72.07%
Human Ether-a-go-go-Related Gene inhibition + 0.7041 70.41%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.9298 92.98%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.8364 83.64%
Acute Oral Toxicity (c) III 0.6871 68.71%
Estrogen receptor binding + 0.9084 90.84%
Androgen receptor binding + 0.7768 77.68%
Thyroid receptor binding + 0.7278 72.78%
Glucocorticoid receptor binding + 0.8969 89.69%
Aromatase binding + 0.8552 85.52%
PPAR gamma + 0.5398 53.98%
Honey bee toxicity - 0.8033 80.33%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9813 98.13%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.31% 97.25%
CHEMBL1871 P10275 Androgen Receptor 95.83% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 95.73% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.89% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.63% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.53% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.24% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.69% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.22% 96.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.53% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.69% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.61% 98.95%
CHEMBL4208 P20618 Proteasome component C5 82.70% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.71% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.55% 91.07%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.01% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.66% 97.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Dioscorea bulbifera

Cross-Links

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PubChem 44606588
LOTUS LTS0141598
wikiData Q105253740