Propylcyclopropane

Details

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Internal ID 02d2dc6a-4e70-467a-86c7-d04835273c4f
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name propylcyclopropane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12/c1-2-3-6-4-5-6/h6H,2-5H2,1H3
InChI Key MWVPQZRIWVPJCA-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12
Molecular Weight 84.16 g/mol
Exact Mass 84.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Cyclopropane, propyl-
Propane, 1-cyclopropyl-
DTXSID20178851
Cyclopropane, propyl
RefChem:176533
DTXCID80101342
MWVPQZRIWVPJCA-UHFFFAOYSA-N
2415-72-7
SCHEMBL5172
SCHEMBL22771
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Propylcyclopropane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9898 98.98%
Caco-2 + 0.8862 88.62%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5147 51.47%
OATP2B1 inhibitior - 0.8430 84.30%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9575 95.75%
P-glycoprotein inhibitior - 0.9892 98.92%
P-glycoprotein substrate - 0.9162 91.62%
CYP3A4 substrate - 0.7417 74.17%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9821 98.21%
CYP2C9 inhibition - 0.8926 89.26%
CYP2C19 inhibition - 0.9190 91.90%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.6317 63.17%
CYP2C8 inhibition - 0.9632 96.32%
CYP inhibitory promiscuity - 0.7417 74.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.4689 46.89%
Eye corrosion + 0.9887 98.87%
Eye irritation + 0.9891 98.91%
Skin irritation + 0.7809 78.09%
Skin corrosion - 0.9812 98.12%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6910 69.10%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6979 69.79%
skin sensitisation + 0.9063 90.63%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7563 75.63%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6302 63.02%
Acute Oral Toxicity (c) III 0.5918 59.18%
Estrogen receptor binding - 0.9263 92.63%
Androgen receptor binding - 0.9575 95.75%
Thyroid receptor binding - 0.8858 88.58%
Glucocorticoid receptor binding - 0.9045 90.45%
Aromatase binding - 0.8583 85.83%
PPAR gamma - 0.9177 91.77%
Honey bee toxicity - 0.9579 95.79%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9545 95.45%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.50% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.64% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.99% 97.09%
CHEMBL2581 P07339 Cathepsin D 86.78% 98.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.79% 96.61%
CHEMBL230 P35354 Cyclooxygenase-2 83.38% 89.63%
CHEMBL226 P30542 Adenosine A1 receptor 82.78% 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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 17014
NPASS NPC235265