(E,6R)-2-methyl-6-[(1S,2R,3R,4R,11S,15S)-4-methyl-12-methylidene-15-tetracyclo[9.4.0.02,4.03,8]pentadec-7-enyl]hept-2-enoic acid

Details

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Internal ID c391f4e4-d460-4b0a-b2b5-7466fb8964b7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name (E,6R)-2-methyl-6-[(1S,2R,3R,4R,11S,15S)-4-methyl-12-methylidene-15-tetracyclo[9.4.0.02,4.03,8]pentadec-7-enyl]hept-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H36O2/c1-15(7-5-8-17(3)24(26)27)19-12-10-16(2)20-13-11-18-9-6-14-25(4)22(18)23(25)21(19)20/h8-9,15,19-23H,2,5-7,10-14H2,1,3-4H3,(H,26,27)/b17-8+/t15-,19+,20-,21+,22+,23-,25+/m1/s1
InChI Key KAAGZIORAICENU-IIAIHXIISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H36O2
Molecular Weight 368.60 g/mol
Exact Mass 368.271530387 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.10
Atomic LogP (AlogP) 6.40
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,6R)-2-methyl-6-[(1S,2R,3R,4R,11S,15S)-4-methyl-12-methylidene-15-tetracyclo[9.4.0.02,4.03,8]pentadec-7-enyl]hept-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.5760 57.60%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Plasma membrane 0.3843 38.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8079 80.79%
OATP1B3 inhibitior - 0.2424 24.24%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8352 83.52%
P-glycoprotein inhibitior - 0.5896 58.96%
P-glycoprotein substrate - 0.6705 67.05%
CYP3A4 substrate + 0.6359 63.59%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.9180 91.80%
CYP3A4 inhibition - 0.9025 90.25%
CYP2C9 inhibition + 0.6668 66.68%
CYP2C19 inhibition + 0.5644 56.44%
CYP2D6 inhibition - 0.9092 90.92%
CYP1A2 inhibition - 0.6322 63.22%
CYP2C8 inhibition - 0.6011 60.11%
CYP inhibitory promiscuity - 0.7975 79.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6364 63.64%
Eye corrosion - 0.9720 97.20%
Eye irritation - 0.9396 93.96%
Skin irritation - 0.6302 63.02%
Skin corrosion - 0.9693 96.93%
Ames mutagenesis - 0.6647 66.47%
Human Ether-a-go-go-Related Gene inhibition + 0.7033 70.33%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5331 53.31%
skin sensitisation + 0.5815 58.15%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8359 83.59%
Acute Oral Toxicity (c) III 0.8208 82.08%
Estrogen receptor binding + 0.7861 78.61%
Androgen receptor binding + 0.7244 72.44%
Thyroid receptor binding + 0.6083 60.83%
Glucocorticoid receptor binding + 0.7628 76.28%
Aromatase binding + 0.6757 67.57%
PPAR gamma + 0.5538 55.38%
Honey bee toxicity - 0.8739 87.39%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.44% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.45% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.64% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.89% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.48% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.83% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.10% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 88.92% 91.19%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.87% 96.47%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.45% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.09% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.85% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.78% 94.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.74% 95.89%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 85.53% 97.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.69% 93.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.95% 89.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.19% 96.38%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.36% 93.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.03% 90.71%
CHEMBL5028 O14672 ADAM10 80.78% 97.50%
CHEMBL1937 Q92769 Histone deacetylase 2 80.16% 94.75%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.06% 98.75%

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.
There are no matching plants.

Cross-Links

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PubChem 101932326
LOTUS LTS0035519
wikiData Q105137755