7-ethenyl-2,6-dihydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carbaldehyde

Details

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Internal ID 30801590-87da-4bf6-b516-ca227bf910ea
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Hydroxysteroids
IUPAC Name 7-ethenyl-2,6-dihydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O3/c1-5-18(2)11-13-6-7-15-19(3,14(13)10-17(18)23)9-8-16(22)20(15,4)12-21/h5,11-12,14-17,22-23H,1,6-10H2,2-4H3
InChI Key FLRZSIWHIJTYQM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O3
Molecular Weight 318.40 g/mol
Exact Mass 318.21949481 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.5744 57.44%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7254 72.54%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9134 91.34%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.7000 70.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8854 88.54%
P-glycoprotein substrate - 0.7531 75.31%
CYP3A4 substrate + 0.6424 64.24%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.7083 70.83%
CYP3A4 inhibition - 0.7187 71.87%
CYP2C9 inhibition - 0.8327 83.27%
CYP2C19 inhibition - 0.7949 79.49%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.8411 84.11%
CYP2C8 inhibition - 0.7494 74.94%
CYP inhibitory promiscuity - 0.9116 91.16%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4771 47.71%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9297 92.97%
Skin irritation + 0.6106 61.06%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5084 50.84%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5209 52.09%
skin sensitisation - 0.6313 63.13%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7366 73.66%
Acute Oral Toxicity (c) I 0.4403 44.03%
Estrogen receptor binding + 0.7690 76.90%
Androgen receptor binding + 0.6093 60.93%
Thyroid receptor binding + 0.6951 69.51%
Glucocorticoid receptor binding + 0.7516 75.16%
Aromatase binding + 0.5894 58.94%
PPAR gamma + 0.5620 56.20%
Honey bee toxicity - 0.8373 83.73%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.70% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.51% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.50% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.67% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.18% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.41% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.07% 95.89%
CHEMBL5028 O14672 ADAM10 81.88% 97.50%

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.
Euphorbia quinquecostata

Cross-Links

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PubChem 85362190
LOTUS LTS0262897
wikiData Q104997430