(1R,4aR,6S,8aS,10aR)-6-ethenyl-1,4a,6-trimethyl-3,4,7,8,8a,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid

Details

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Internal ID dee69265-ce1d-476e-a586-49bb0317d369
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name (1R,4aR,6S,8aS,10aR)-6-ethenyl-1,4a,6-trimethyl-3,4,7,8,8a,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O2/c1-5-18(2)12-9-14-7-8-16-19(3,15(14)13-18)10-6-11-20(16,4)17(21)22/h5,13-14,16H,1,6-12H2,2-4H3,(H,21,22)/t14-,16+,18+,19-,20+/m0/s1
InChI Key RRYPRCLLARNSER-XTDQBWQRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O2
Molecular Weight 302.50 g/mol
Exact Mass 302.224580195 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.21
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4aR,6S,8aS,10aR)-6-ethenyl-1,4a,6-trimethyl-3,4,7,8,8a,9,10,10a-octahydro-2H-phenanthrene-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 + 0.9962 99.62%
Caco-2 + 0.8284 82.84%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.4127 41.27%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8996 89.96%
OATP1B3 inhibitior - 0.4703 47.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.7733 77.33%
P-glycoprotein inhibitior - 0.7233 72.33%
P-glycoprotein substrate - 0.8785 87.85%
CYP3A4 substrate + 0.5430 54.30%
CYP2C9 substrate - 0.5859 58.59%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.8276 82.76%
CYP2C9 inhibition + 0.8949 89.49%
CYP2C19 inhibition + 0.7575 75.75%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.7748 77.48%
CYP2C8 inhibition - 0.5651 56.51%
CYP inhibitory promiscuity - 0.8959 89.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5883 58.83%
Eye corrosion - 0.9683 96.83%
Eye irritation - 0.8609 86.09%
Skin irritation - 0.6521 65.21%
Skin corrosion - 0.9781 97.81%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6662 66.62%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.7018 70.18%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7047 70.47%
Acute Oral Toxicity (c) III 0.7692 76.92%
Estrogen receptor binding + 0.6323 63.23%
Androgen receptor binding + 0.5328 53.28%
Thyroid receptor binding + 0.7071 70.71%
Glucocorticoid receptor binding + 0.6724 67.24%
Aromatase binding + 0.7585 75.85%
PPAR gamma - 0.5572 55.72%
Honey bee toxicity - 0.9154 91.54%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.50% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.82% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.35% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.44% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.70% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 84.71% 91.19%
CHEMBL2581 P07339 Cathepsin D 82.70% 98.95%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.60% 82.05%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.58% 93.00%

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.
Coleonema pulchellum

Cross-Links

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PubChem 163190537
LOTUS LTS0257819
wikiData Q105244453