7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-4,5,9-triol

Details

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Internal ID 515a54c4-6775-4a7a-80f9-95cfec3ce3c4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-4,5,9-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O3/c1-6-19(4)10-12-13(21)9-15-18(2,3)8-7-16(23)20(15,5)17(12)14(22)11-19/h6,10,13-17,21-23H,1,7-9,11H2,2-5H3
InChI Key GPSPSNASZGKBJQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O3
Molecular Weight 320.50 g/mol
Exact Mass 320.23514488 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-4,5,9-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.5540 55.40%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6736 67.36%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9233 92.33%
OATP1B3 inhibitior + 0.9334 93.34%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.6351 63.51%
P-glycoprotein inhibitior - 0.8513 85.13%
P-glycoprotein substrate - 0.7583 75.83%
CYP3A4 substrate + 0.6299 62.99%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.7736 77.36%
CYP2C9 inhibition - 0.8846 88.46%
CYP2C19 inhibition - 0.8091 80.91%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.8949 89.49%
CYP2C8 inhibition - 0.6550 65.50%
CYP inhibitory promiscuity - 0.8019 80.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6196 61.96%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9712 97.12%
Skin irritation + 0.5200 52.00%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.7323 73.23%
Human Ether-a-go-go-Related Gene inhibition - 0.4094 40.94%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5092 50.92%
skin sensitisation + 0.5320 53.20%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6364 63.64%
Acute Oral Toxicity (c) III 0.7663 76.63%
Estrogen receptor binding + 0.6409 64.09%
Androgen receptor binding + 0.5601 56.01%
Thyroid receptor binding + 0.6416 64.16%
Glucocorticoid receptor binding + 0.6563 65.63%
Aromatase binding + 0.5325 53.25%
PPAR gamma - 0.5863 58.63%
Honey bee toxicity - 0.7737 77.37%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9951 99.51%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.49% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.59% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.13% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.87% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.56% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.07% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.45% 91.07%
CHEMBL1937 Q92769 Histone deacetylase 2 80.78% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.67% 82.69%

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.
Kaempferia marginata

Cross-Links

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PubChem 73015996
LOTUS LTS0036441
wikiData Q105015101