3-Cyclohexen-1-ol

Details

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Internal ID 25964a56-79b8-4a2e-a952-e14c70ab7b14
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name cyclohex-3-en-1-ol
SMILES (Canonical) C1CC(CC=C1)O
SMILES (Isomeric) C1CC(CC=C1)O
InChI InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h1-2,6-7H,3-5H2
InChI Key ABZZOPIABWYXSN-UHFFFAOYSA-N
Popularity 37 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 1.10
Atomic LogP (AlogP) 1.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Cyclohex-3-en-1-ol
822-66-2
Cyclohex-3-enol
3-Cyclohexenol
1-HYDROXY-3-CYCLOHEXENE
MFCD00040176
Cyclohexen-4-ol
4-Hydroxycyclohexene
3-Cyclohexene-1-ol
Cyclohex-1-en-4-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Cyclohexen-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 + 0.9958 99.58%
Caco-2 + 0.6868 68.68%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6047 60.47%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9700 97.00%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9532 95.32%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.7059 70.59%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7046 70.46%
CYP3A4 inhibition - 0.9673 96.73%
CYP2C9 inhibition - 0.9351 93.51%
CYP2C19 inhibition - 0.9383 93.83%
CYP2D6 inhibition - 0.9631 96.31%
CYP1A2 inhibition - 0.8595 85.95%
CYP2C8 inhibition - 0.9742 97.42%
CYP inhibitory promiscuity - 0.9343 93.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6739 67.39%
Eye corrosion + 0.9478 94.78%
Eye irritation + 0.9749 97.49%
Skin irritation + 0.8717 87.17%
Skin corrosion - 0.8590 85.90%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6843 68.43%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation + 0.7638 76.38%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7516 75.16%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6036 60.36%
Estrogen receptor binding - 0.9404 94.04%
Androgen receptor binding - 0.8892 88.92%
Thyroid receptor binding - 0.9114 91.14%
Glucocorticoid receptor binding - 0.8615 86.15%
Aromatase binding - 0.8969 89.69%
PPAR gamma - 0.9067 90.67%
Honey bee toxicity - 0.8924 89.24%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.5659 56.59%

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 87.89% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.17% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.22% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.05% 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.
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 556685
NPASS NPC27241