Methylcyclopentane

Details

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Internal ID 19e0d593-56e2-44f7-a122-6ac4814aa134
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name methylcyclopentane
SMILES (Canonical) CC1CCCC1
SMILES (Isomeric) CC1CCCC1
InChI InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3
InChI Key GDOPTJXRTPNYNR-UHFFFAOYSA-N
Popularity 1,455 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 3.40
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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96-37-7
Cyclopentane, methyl-
Methyl cyclopentane
Methylpentamethylene
Methyl-cyclopentane
5G26CC1ASK
DTXSID3025590
CHEBI:88429
NSC-24836
DTXCID205590
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methylcyclopentane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.8312 83.12%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.7492 74.92%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.9764 97.64%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9688 96.88%
P-glycoprotein inhibitior - 0.9874 98.74%
P-glycoprotein substrate - 0.9850 98.50%
CYP3A4 substrate - 0.7583 75.83%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7481 74.81%
CYP3A4 inhibition - 0.9832 98.32%
CYP2C9 inhibition - 0.9416 94.16%
CYP2C19 inhibition - 0.9389 93.89%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition - 0.7575 75.75%
CYP2C8 inhibition - 0.9936 99.36%
CYP inhibitory promiscuity - 0.8930 89.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4384 43.84%
Eye corrosion + 0.9885 98.85%
Eye irritation + 0.9957 99.57%
Skin irritation + 0.9037 90.37%
Skin corrosion - 0.9677 96.77%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7535 75.35%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7209 72.09%
skin sensitisation + 0.8079 80.79%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7543 75.43%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5254 52.54%
Acute Oral Toxicity (c) III 0.6182 61.82%
Estrogen receptor binding - 0.9294 92.94%
Androgen receptor binding - 0.9260 92.60%
Thyroid receptor binding - 0.8682 86.82%
Glucocorticoid receptor binding - 0.9020 90.20%
Aromatase binding - 0.8789 87.89%
PPAR gamma - 0.9333 93.33%
Honey bee toxicity - 0.9522 95.22%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9315 93.15%

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 90.39% 97.25%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 86.84% 95.27%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.19% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.66% 99.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.47% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.69% 86.00%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 80.73% 90.71%
CHEMBL237 P41145 Kappa opioid receptor 80.18% 98.10%

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.
Glycyrrhiza

Cross-Links

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PubChem 7296
NPASS NPC59846
LOTUS LTS0046578
wikiData Q412979