(1R)-4-methyl-1-propan-2-ylcyclohex-2-en-1-ol

Details

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Internal ID bdae7f39-2ad1-4cfb-98b9-452d59bcb6bf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (1R)-4-methyl-1-propan-2-ylcyclohex-2-en-1-ol
SMILES (Canonical) CC1CCC(C=C1)(C(C)C)O
SMILES (Isomeric) CC1CC[C@](C=C1)(C(C)C)O
InChI InChI=1S/C10H18O/c1-8(2)10(11)6-4-9(3)5-7-10/h4,6,8-9,11H,5,7H2,1-3H3/t9?,10-/m1/s1
InChI Key BJOGDSZCIIOXEK-QVDQXJPCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R)-4-methyl-1-propan-2-ylcyclohex-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 + 0.9957 99.57%
Caco-2 + 0.7267 72.67%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4609 46.09%
OATP2B1 inhibitior - 0.8489 84.89%
OATP1B1 inhibitior + 0.9677 96.77%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9418 94.18%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9188 91.88%
CYP3A4 substrate - 0.5581 55.81%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.7764 77.64%
CYP3A4 inhibition - 0.8899 88.99%
CYP2C9 inhibition - 0.8617 86.17%
CYP2C19 inhibition - 0.8965 89.65%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition - 0.7875 78.75%
CYP2C8 inhibition - 0.9783 97.83%
CYP inhibitory promiscuity - 0.9491 94.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6523 65.23%
Eye corrosion - 0.6566 65.66%
Eye irritation + 0.7686 76.86%
Skin irritation + 0.8650 86.50%
Skin corrosion - 0.7785 77.85%
Ames mutagenesis - 0.6370 63.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6157 61.57%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6120 61.20%
skin sensitisation + 0.9066 90.66%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6369 63.69%
Acute Oral Toxicity (c) III 0.8912 89.12%
Estrogen receptor binding - 0.9489 94.89%
Androgen receptor binding - 0.8384 83.84%
Thyroid receptor binding - 0.7475 74.75%
Glucocorticoid receptor binding - 0.8121 81.21%
Aromatase binding - 0.9275 92.75%
PPAR gamma - 0.8770 87.70%
Honey bee toxicity - 0.9115 91.15%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.6460 64.60%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.76% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.68% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.41% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.28% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.96% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 84.69% 95.93%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.46% 86.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.85% 94.80%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.70% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 82.24% 90.17%
CHEMBL4072 P07858 Cathepsin B 81.96% 93.67%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 81.08% 99.00%
CHEMBL238 Q01959 Dopamine transporter 80.46% 95.88%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.14% 100.00%

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.
Haplopappus foliosus

Cross-Links

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PubChem 163187984
LOTUS LTS0043120
wikiData Q104937214