(1S,2S)-1,2-dimethylcyclopentane

Details

Top
Internal ID f0b7b417-7818-4487-98d0-211290675cb8
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name (1S,2S)-1,2-dimethylcyclopentane
SMILES (Canonical) CC1CCCC1C
SMILES (Isomeric) C[C@H]1CCC[C@@H]1C
InChI InChI=1S/C7H14/c1-6-4-3-5-7(6)2/h6-7H,3-5H2,1-2H3/t6-,7-/m0/s1
InChI Key RIRARCHMRDHZAR-BQBZGAKWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H14
Molecular Weight 98.19 g/mol
Exact Mass 98.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
SCHEMBL597948
trans-1,2-dimethylcyclopentan
AKOS006273274
(1S)-trans-1,2-dimethyl-cyclopentane
cyclopentane, 1,2-dimethyl-, (1S,2S)-
NS00079543
InChI=1/C7H14/c1-6-4-3-5-7(6)2/h6-7H,3-5H2,1-2H3/t6-,7-/m0/s

2D Structure

Top
2D Structure of (1S,2S)-1,2-dimethylcyclopentane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.8089 80.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.7446 74.46%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.9706 97.06%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9530 95.30%
P-glycoprotein inhibitior - 0.9830 98.30%
P-glycoprotein substrate - 0.9889 98.89%
CYP3A4 substrate - 0.7326 73.26%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7481 74.81%
CYP3A4 inhibition - 0.9803 98.03%
CYP2C9 inhibition - 0.9377 93.77%
CYP2C19 inhibition - 0.9323 93.23%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition - 0.7579 75.79%
CYP2C8 inhibition - 0.9945 99.45%
CYP inhibitory promiscuity - 0.8846 88.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.4903 49.03%
Eye corrosion + 0.9362 93.62%
Eye irritation + 0.9954 99.54%
Skin irritation + 0.7989 79.89%
Skin corrosion - 0.9858 98.58%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7112 71.12%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7907 79.07%
skin sensitisation + 0.8570 85.70%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6057 60.57%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4840 48.40%
Acute Oral Toxicity (c) IV 0.5782 57.82%
Estrogen receptor binding - 0.9287 92.87%
Androgen receptor binding - 0.8264 82.64%
Thyroid receptor binding - 0.8730 87.30%
Glucocorticoid receptor binding - 0.8910 89.10%
Aromatase binding - 0.8700 87.00%
PPAR gamma - 0.9318 93.18%
Honey bee toxicity - 0.9389 93.89%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.8500 85.00%
Fish aquatic toxicity + 0.9677 96.77%

Targets

Top

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 85.48% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.89% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.00% 99.18%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.25% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.20% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.47% 92.94%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.14% 95.27%

Plants that contains it

Top
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

Top
PubChem 641612
NPASS NPC66739