Cyclohexanecarboxaldehyde

Details

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Internal ID 05429c08-584d-4f33-892f-d439f370b16d
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name cyclohexanecarbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O/c8-6-7-4-2-1-3-5-7/h6-7H,1-5H2
InChI Key KVFDZFBHBWTVID-UHFFFAOYSA-N
Popularity 906 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O
Molecular Weight 112.17 g/mol
Exact Mass 112.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2043-61-0
Cyclohexanecarbaldehyde
Cyclohexanal
Formylcyclohexane
Cyclohexanealdehyde
Hexahydrobenzaldehyde
Cyclohexanaldehyde
Cyclohexylcarboxaldehyde
1-Formylcyclohexane
Cyclohexylformaldehyde
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclohexanecarboxaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.6103 61.03%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4870 48.70%
OATP2B1 inhibitior - 0.8452 84.52%
OATP1B1 inhibitior + 0.9564 95.64%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9616 96.16%
P-glycoprotein inhibitior - 0.9890 98.90%
P-glycoprotein substrate - 0.9915 99.15%
CYP3A4 substrate - 0.7310 73.10%
CYP2C9 substrate - 0.6198 61.98%
CYP2D6 substrate - 0.7375 73.75%
CYP3A4 inhibition - 0.9794 97.94%
CYP2C9 inhibition - 0.9393 93.93%
CYP2C19 inhibition - 0.9599 95.99%
CYP2D6 inhibition - 0.9798 97.98%
CYP1A2 inhibition - 0.8064 80.64%
CYP2C8 inhibition - 0.9772 97.72%
CYP inhibitory promiscuity - 0.8835 88.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6889 68.89%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9936 99.36%
Skin irritation + 0.8797 87.97%
Skin corrosion - 0.6506 65.06%
Ames mutagenesis - 0.8347 83.47%
Human Ether-a-go-go-Related Gene inhibition - 0.6485 64.85%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6355 63.55%
skin sensitisation + 0.7165 71.65%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.4783 47.83%
Acute Oral Toxicity (c) III 0.6753 67.53%
Estrogen receptor binding - 0.8293 82.93%
Androgen receptor binding - 0.9070 90.70%
Thyroid receptor binding - 0.8473 84.73%
Glucocorticoid receptor binding - 0.8304 83.04%
Aromatase binding - 0.7428 74.28%
PPAR gamma - 0.8799 87.99%
Honey bee toxicity - 0.9105 91.05%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.7659 76.59%

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
CHEMBL3012 Q13946 Phosphodiesterase 7A 89.07% 99.29%
CHEMBL5203 P33316 dUTP pyrophosphatase 86.03% 99.18%
CHEMBL2664 P23526 Adenosylhomocysteinase 84.65% 86.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.53% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.98% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.97% 95.50%
CHEMBL1968 P07099 Epoxide hydrolase 1 80.74% 98.57%

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.
Gossypium hirsutum

Cross-Links

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PubChem 16275
LOTUS LTS0187117
wikiData Q72459569