(1R,4R)-2,5,5-trimethyl-4-(4-methylpent-3-enyl)cyclohex-2-en-1-ol

Details

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Internal ID ab25c8b8-abba-436d-add1-6e54a9321130
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (1R,4R)-2,5,5-trimethyl-4-(4-methylpent-3-enyl)cyclohex-2-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O/c1-11(2)7-6-8-13-9-12(3)14(16)10-15(13,4)5/h7,9,13-14,16H,6,8,10H2,1-5H3/t13-,14-/m1/s1
InChI Key XJGGQZRGBNCENL-ZIAGYGMSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4R)-2,5,5-trimethyl-4-(4-methylpent-3-enyl)cyclohex-2-en-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.8138 81.38%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4466 44.66%
OATP2B1 inhibitior - 0.8476 84.76%
OATP1B1 inhibitior + 0.8727 87.27%
OATP1B3 inhibitior + 0.9237 92.37%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8745 87.45%
P-glycoprotein inhibitior - 0.9267 92.67%
P-glycoprotein substrate - 0.8969 89.69%
CYP3A4 substrate - 0.5316 53.16%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.7263 72.63%
CYP3A4 inhibition - 0.8312 83.12%
CYP2C9 inhibition - 0.9141 91.41%
CYP2C19 inhibition - 0.9179 91.79%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.8873 88.73%
CYP2C8 inhibition - 0.9666 96.66%
CYP inhibitory promiscuity - 0.8524 85.24%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6698 66.98%
Eye corrosion - 0.9346 93.46%
Eye irritation - 0.4800 48.00%
Skin irritation + 0.7258 72.58%
Skin corrosion - 0.9741 97.41%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5090 50.90%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.9096 90.96%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5297 52.97%
Acute Oral Toxicity (c) III 0.8305 83.05%
Estrogen receptor binding - 0.7691 76.91%
Androgen receptor binding - 0.9030 90.30%
Thyroid receptor binding - 0.7161 71.61%
Glucocorticoid receptor binding - 0.5344 53.44%
Aromatase binding - 0.7171 71.71%
PPAR gamma - 0.5803 58.03%
Honey bee toxicity - 0.8894 88.94%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9565 95.65%

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 91.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.75% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.80% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 87.51% 94.75%
CHEMBL221 P23219 Cyclooxygenase-1 86.67% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 84.85% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.04% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.86% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.56% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162934757
LOTUS LTS0047506
wikiData Q105328933