Cyclopropylmethanol

Details

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Internal ID 74840bbf-c4bd-44bf-9e4b-2804a05992f0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name cyclopropylmethanol
SMILES (Canonical) C1CC1CO
SMILES (Isomeric) C1CC1CO
InChI InChI=1S/C4H8O/c5-3-4-1-2-4/h4-5H,1-3H2
InChI Key GUDMZGLFZNLYEY-UHFFFAOYSA-N
Popularity 163 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O
Molecular Weight 72.11 g/mol
Exact Mass 72.057514874 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Cyclopropanemethanol
2516-33-8
Cyclopropyl carbinol
Cyclopropylcarbinol
Cyclopropylmethyl alcohol
(Hydroxymethyl)cyclopropane
Cyclopropanemethyl alcohol
Cyclopropylcarbinyl alcohol
Hydroxymethylcyclopropane
MFCD00001309
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclopropylmethanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9739 97.39%
Caco-2 + 0.4907 49.07%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4909 49.09%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9744 97.44%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9510 95.10%
P-glycoprotein inhibitior - 0.9885 98.85%
P-glycoprotein substrate - 0.9841 98.41%
CYP3A4 substrate - 0.7929 79.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6937 69.37%
CYP3A4 inhibition - 0.9576 95.76%
CYP2C9 inhibition - 0.8243 82.43%
CYP2C19 inhibition - 0.8551 85.51%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.6802 68.02%
CYP2C8 inhibition - 0.9866 98.66%
CYP inhibitory promiscuity - 0.8953 89.53%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5287 52.87%
Eye corrosion + 0.9615 96.15%
Eye irritation + 0.9864 98.64%
Skin irritation + 0.7373 73.73%
Skin corrosion + 0.5503 55.03%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7044 70.44%
Micronuclear - 0.8241 82.41%
Hepatotoxicity + 0.5326 53.26%
skin sensitisation + 0.5512 55.12%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5308 53.08%
Acute Oral Toxicity (c) III 0.4785 47.85%
Estrogen receptor binding - 0.9215 92.15%
Androgen receptor binding - 0.9392 93.92%
Thyroid receptor binding - 0.8717 87.17%
Glucocorticoid receptor binding - 0.8681 86.81%
Aromatase binding - 0.8523 85.23%
PPAR gamma - 0.9065 90.65%
Honey bee toxicity - 0.9366 93.66%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.6914 69.14%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 91.64% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.43% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.12% 97.25%
CHEMBL237 P41145 Kappa opioid receptor 84.62% 98.10%
CHEMBL226 P30542 Adenosine A1 receptor 83.70% 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.
Hypericum japonicum
Portulaca oleracea

Cross-Links

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PubChem 75644
NPASS NPC198778