7-Ethenyl-8,8a,9-trihydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-1-carboxylic acid

Details

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Internal ID e7b6d460-7b1b-43d3-bf77-b9e5ffe6ee41
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 7-ethenyl-8,8a,9-trihydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O5/c1-5-17(2)10-7-12-18(3)8-6-9-19(4,16(23)24)13(18)11-14(21)20(12,25)15(17)22/h5,12-15,21-22,25H,1,6-11H2,2-4H3,(H,23,24)
InChI Key KSAYCDQHYVZYAT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O5
Molecular Weight 352.50 g/mol
Exact Mass 352.22497412 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.34
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Ethenyl-8,8a,9-trihydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9382 93.82%
Caco-2 - 0.5894 58.94%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6795 67.95%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.8568 85.68%
OATP1B3 inhibitior + 0.7948 79.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8071 80.71%
BSEP inhibitior + 0.6547 65.47%
P-glycoprotein inhibitior - 0.8717 87.17%
P-glycoprotein substrate - 0.8862 88.62%
CYP3A4 substrate + 0.5985 59.85%
CYP2C9 substrate - 0.8101 81.01%
CYP2D6 substrate - 0.8674 86.74%
CYP3A4 inhibition - 0.6786 67.86%
CYP2C9 inhibition - 0.8874 88.74%
CYP2C19 inhibition - 0.8213 82.13%
CYP2D6 inhibition - 0.9615 96.15%
CYP1A2 inhibition - 0.7715 77.15%
CYP2C8 inhibition - 0.7404 74.04%
CYP inhibitory promiscuity - 0.9868 98.68%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6842 68.42%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9528 95.28%
Skin irritation + 0.6333 63.33%
Skin corrosion - 0.9150 91.50%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7090 70.90%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6334 63.34%
skin sensitisation - 0.7557 75.57%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6477 64.77%
Acute Oral Toxicity (c) III 0.5130 51.30%
Estrogen receptor binding + 0.7970 79.70%
Androgen receptor binding - 0.4908 49.08%
Thyroid receptor binding + 0.7268 72.68%
Glucocorticoid receptor binding + 0.8273 82.73%
Aromatase binding + 0.7397 73.97%
PPAR gamma - 0.5525 55.25%
Honey bee toxicity - 0.8523 85.23%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9934 99.34%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.80% 94.45%
CHEMBL237 P41145 Kappa opioid receptor 88.27% 98.10%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.12% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 86.44% 91.19%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.47% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.48% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.91% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.78% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.53% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.23% 93.04%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.21% 91.11%
CHEMBL1902 P62942 FK506-binding protein 1A 80.09% 97.05%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.01% 91.07%

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.
Vellozia patens

Cross-Links

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PubChem 162967664
LOTUS LTS0012304
wikiData Q105145333