3-Cyclohexene-1-methanol, (R)-

Details

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Internal ID bc6f43d8-a734-407f-927b-a4af245fe422
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name [(1R)-cyclohex-3-en-1-yl]methanol
SMILES (Canonical) C1CC(CC=C1)CO
SMILES (Isomeric) C1C[C@H](CC=C1)CO
InChI InChI=1S/C7H12O/c8-6-7-4-2-1-3-5-7/h1-2,7-8H,3-6H2/t7-/m0/s1
InChI Key VEIYJWQZNGASMA-ZETCQYMHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O
Molecular Weight 112.17 g/mol
Exact Mass 112.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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3-Cyclohexene-1beta-methanol
5709-99-9
SCHEMBL10516170
DTXSID30486156

2D Structure

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2D Structure of 3-Cyclohexene-1-methanol, (R)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 + 0.6749 67.49%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4510 45.10%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9621 96.21%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9491 94.91%
P-glycoprotein inhibitior - 0.9894 98.94%
P-glycoprotein substrate - 0.9652 96.52%
CYP3A4 substrate - 0.7046 70.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7284 72.84%
CYP3A4 inhibition - 0.9269 92.69%
CYP2C9 inhibition - 0.8244 82.44%
CYP2C19 inhibition - 0.8655 86.55%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.7528 75.28%
CYP2C8 inhibition - 0.9488 94.88%
CYP inhibitory promiscuity - 0.7934 79.34%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6587 65.87%
Eye corrosion + 0.9417 94.17%
Eye irritation + 0.9334 93.34%
Skin irritation + 0.5346 53.46%
Skin corrosion - 0.9273 92.73%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5462 54.62%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation + 0.8380 83.80%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4805 48.05%
Acute Oral Toxicity (c) III 0.8720 87.20%
Estrogen receptor binding - 0.9500 95.00%
Androgen receptor binding - 0.8915 89.15%
Thyroid receptor binding - 0.8964 89.64%
Glucocorticoid receptor binding - 0.8722 87.22%
Aromatase binding - 0.7802 78.02%
PPAR gamma - 0.8640 86.40%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7830 78.30%

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 92.44% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.39% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.12% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.69% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 85.26% 95.93%

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.
Tetradium ruticarpum

Cross-Links

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PubChem 12299190
NPASS NPC129472