(1R,4aR,7S,10aR)-7-ethenyl-1,4a,7,10a-tetramethyl-2,3,4,5,6,8,9,10-octahydrophenanthrene-1-carboxylic acid

Details

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Internal ID f86d04cf-4903-45dc-8c97-1b2de2e06f9b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1R,4aR,7S,10aR)-7-ethenyl-1,4a,7,10a-tetramethyl-2,3,4,5,6,8,9,10-octahydrophenanthrene-1-carboxylic acid
SMILES (Canonical) CC1(CCC2=C(C1)CCC3(C2(CCCC3(C)C(=O)O)C)C)C=C
SMILES (Isomeric) C[C@@]1(CCC2=C(C1)CC[C@@]3([C@@]2(CCC[C@@]3(C)C(=O)O)C)C)C=C
InChI InChI=1S/C21H32O2/c1-6-18(2)12-9-16-15(14-18)8-13-21(5)19(16,3)10-7-11-20(21,4)17(22)23/h6H,1,7-14H2,2-5H3,(H,22,23)/t18-,19+,20-,21+/m0/s1
InChI Key UBOGRCPGKWZYDV-JSXRDJHFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O2
Molecular Weight 316.50 g/mol
Exact Mass 316.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.74
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,7S,10aR)-7-ethenyl-1,4a,7,10a-tetramethyl-2,3,4,5,6,8,9,10-octahydrophenanthrene-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 + 0.9961 99.61%
Caco-2 + 0.8672 86.72%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4786 47.86%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.8771 87.71%
OATP1B3 inhibitior - 0.4358 43.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.6868 68.68%
P-glycoprotein inhibitior - 0.8532 85.32%
P-glycoprotein substrate - 0.8905 89.05%
CYP3A4 substrate + 0.5583 55.83%
CYP2C9 substrate - 0.6248 62.48%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.8020 80.20%
CYP2C9 inhibition + 0.7504 75.04%
CYP2C19 inhibition + 0.6461 64.61%
CYP2D6 inhibition - 0.9336 93.36%
CYP1A2 inhibition - 0.7505 75.05%
CYP2C8 inhibition - 0.7926 79.26%
CYP inhibitory promiscuity - 0.8689 86.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5941 59.41%
Eye corrosion - 0.9827 98.27%
Eye irritation - 0.5703 57.03%
Skin irritation - 0.6006 60.06%
Skin corrosion - 0.9767 97.67%
Ames mutagenesis - 0.6562 65.62%
Human Ether-a-go-go-Related Gene inhibition + 0.6693 66.93%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5060 50.60%
skin sensitisation + 0.6904 69.04%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6097 60.97%
Acute Oral Toxicity (c) III 0.7750 77.50%
Estrogen receptor binding - 0.6217 62.17%
Androgen receptor binding + 0.6986 69.86%
Thyroid receptor binding + 0.6424 64.24%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6235 62.35%
PPAR gamma - 0.5828 58.28%
Honey bee toxicity - 0.9128 91.28%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7200 72.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.03% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.32% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.26% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 86.05% 91.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.13% 91.07%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.24% 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.
Platycladus orientalis

Cross-Links

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PubChem 162918247
LOTUS LTS0146988
wikiData Q105269535