Cyclohexyl formate

Details

Top
Internal ID cf229c73-3dc3-43e4-9e99-b9eb02403b78
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name cyclohexyl formate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O2/c8-6-9-7-4-2-1-3-5-7/h6-7H,1-5H2
InChI Key VUXKVKAHWOVIDN-UHFFFAOYSA-N
Popularity 40 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H12O2
Molecular Weight 128.17 g/mol
Exact Mass 128.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
Formic acid, cyclohexyl ester
Cyclohexanol, formate
FEMA No. 2353
UNII-ESO2F2836U
ESO2F2836U
EINECS 224-415-3
NSC 11766
Cyclohexyl ester of formic acid
AI3-30436
NSC-11766
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Cyclohexyl formate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.5348 53.48%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7210 72.10%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9721 97.21%
OATP1B3 inhibitior + 0.9710 97.10%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9739 97.39%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9913 99.13%
CYP3A4 substrate - 0.6711 67.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7853 78.53%
CYP3A4 inhibition - 0.9722 97.22%
CYP2C9 inhibition - 0.8876 88.76%
CYP2C19 inhibition - 0.8159 81.59%
CYP2D6 inhibition - 0.9676 96.76%
CYP1A2 inhibition - 0.9133 91.33%
CYP2C8 inhibition - 0.9286 92.86%
CYP inhibitory promiscuity - 0.9523 95.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8120 81.20%
Carcinogenicity (trinary) Non-required 0.6329 63.29%
Eye corrosion + 0.9729 97.29%
Eye irritation + 0.9885 98.85%
Skin irritation + 0.5790 57.90%
Skin corrosion - 0.9328 93.28%
Ames mutagenesis - 0.7754 77.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5545 55.45%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5593 55.93%
skin sensitisation - 0.6304 63.04%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7883 78.83%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) IV 0.5550 55.50%
Estrogen receptor binding - 0.7759 77.59%
Androgen receptor binding - 0.9072 90.72%
Thyroid receptor binding - 0.8007 80.07%
Glucocorticoid receptor binding - 0.8144 81.44%
Aromatase binding - 0.7354 73.54%
PPAR gamma - 0.8705 87.05%
Honey bee toxicity - 0.7449 74.49%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.4072 40.72%

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
CHEMBL5203 P33316 dUTP pyrophosphatase 89.90% 99.18%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.93% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.90% 97.09%
CHEMBL1968 P07099 Epoxide hydrolase 1 83.94% 98.57%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.73% 94.78%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.95% 95.27%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.29% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.82% 92.62%
CHEMBL5957 P21589 5'-nucleotidase 81.57% 97.78%
CHEMBL5255 O00206 Toll-like receptor 4 81.10% 92.50%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.47% 86.67%

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.
Pterocarpus indicus

Cross-Links

Top
PubChem 20358
NPASS NPC250245