Bicyclo[3.1.1]hept-3-en-2-ol

Details

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Internal ID 9f6ae21f-bcac-4d87-aa51-f6245a0e6290
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name bicyclo[3.1.1]hept-3-en-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O/c8-7-2-1-5-3-6(7)4-5/h1-2,5-8H,3-4H2
InChI Key PNOQCFFXXDNXKF-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O
Molecular Weight 110.15 g/mol
Exact Mass 110.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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77697-45-1
NSC231453
SCHEMBL17027688
DTXSID40310731
NSC-231453

2D Structure

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2D Structure of Bicyclo[3.1.1]hept-3-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 - 0.6653 66.53%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4256 42.56%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9704 97.04%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9698 96.98%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9714 97.14%
CYP3A4 substrate - 0.7163 71.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7323 73.23%
CYP3A4 inhibition - 0.9144 91.44%
CYP2C9 inhibition - 0.7875 78.75%
CYP2C19 inhibition - 0.5293 52.93%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition + 0.6073 60.73%
CYP2C8 inhibition - 0.9828 98.28%
CYP inhibitory promiscuity - 0.7997 79.97%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7210 72.10%
Carcinogenicity (trinary) Non-required 0.4938 49.38%
Eye corrosion + 0.5557 55.57%
Eye irritation + 0.7133 71.33%
Skin irritation + 0.7483 74.83%
Skin corrosion - 0.6192 61.92%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7349 73.49%
Micronuclear - 0.6465 64.65%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation + 0.8674 86.74%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4847 48.47%
Acute Oral Toxicity (c) III 0.5058 50.58%
Estrogen receptor binding - 0.8946 89.46%
Androgen receptor binding - 0.8550 85.50%
Thyroid receptor binding - 0.8369 83.69%
Glucocorticoid receptor binding - 0.7326 73.26%
Aromatase binding - 0.8828 88.28%
PPAR gamma - 0.8923 89.23%
Honey bee toxicity - 0.7342 73.42%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.7092 70.92%

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 87.73% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.84% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.77% 91.11%

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.
Abrus melanospermus subsp. melanospermus

Cross-Links

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PubChem 314195
NPASS NPC267889