2-Cyclohexen-1-ol, (1R)-

Details

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Internal ID 814bcb23-d880-4d53-9bf9-ca289a42cb1f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (1R)-cyclohex-2-en-1-ol
SMILES (Canonical) C1CC=CC(C1)O
SMILES (Isomeric) C1CC=C[C@@H](C1)O
InChI InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h2,4,6-7H,1,3,5H2/t6-/m0/s1
InChI Key PQANGXXSEABURG-LURJTMIESA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O
Molecular Weight 98.14 g/mol
Exact Mass 98.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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3413-44-3
2-Cyclohexen-1-ol, (1R)-
(R)-2-Cyclohexen-1-ol
r-2-cyclohexen-1-ol
(1R)-2-Cyclohexen-1-ol
DTXSID80440607
CS-0263308
EN300-86118

2D Structure

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2D Structure of 2-Cyclohexen-1-ol, (1R)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.6462 64.62%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6410 64.10%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9700 97.00%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9589 95.89%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9857 98.57%
CYP3A4 substrate - 0.7140 71.40%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7046 70.46%
CYP3A4 inhibition - 0.9740 97.40%
CYP2C9 inhibition - 0.9308 93.08%
CYP2C19 inhibition - 0.9325 93.25%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition - 0.8380 83.80%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.9311 93.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6591 65.91%
Eye corrosion + 0.9075 90.75%
Eye irritation + 0.9837 98.37%
Skin irritation + 0.8851 88.51%
Skin corrosion - 0.6276 62.76%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6894 68.94%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5218 52.18%
skin sensitisation + 0.7834 78.34%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6406 64.06%
Acute Oral Toxicity (c) III 0.4795 47.95%
Estrogen receptor binding - 0.9328 93.28%
Androgen receptor binding - 0.9426 94.26%
Thyroid receptor binding - 0.8864 88.64%
Glucocorticoid receptor binding - 0.7962 79.62%
Aromatase binding - 0.8896 88.96%
PPAR gamma - 0.8970 89.70%
Honey bee toxicity - 0.8832 88.32%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.7477 74.77%

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 87.56% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 87.13% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.06% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.01% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.85% 96.09%

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.
Foeniculum vulgare
Tetradium ruticarpum
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 10486804
NPASS NPC299539