(R)-(+)-4-Isopropylcyclohex-1-ene-1-carboxaldehyde

Details

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Internal ID 50b28957-b27c-47b4-a6ca-88df3d12b1f4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (4R)-4-propan-2-ylcyclohexene-1-carbaldehyde
SMILES (Canonical) CC(C)C1CCC(=CC1)C=O
SMILES (Isomeric) CC(C)[C@@H]1CCC(=CC1)C=O
InChI InChI=1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,7-8,10H,4-6H2,1-2H3/t10-/m0/s1
InChI Key AEVLWICMAHGAMS-JTQLQIEISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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8950Q87R4M
(R)-(+)-4-Isopropylcyclohex-1-ene-1-carboxaldehyde
94369-75-2
UNII-8950Q87R4M
1-Cyclohexene-1-carboxaldehyde, 4-(1-methylethyl)-, (4R)-
SCHEMBL8844802

2D Structure

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2D Structure of (R)-(+)-4-Isopropylcyclohex-1-ene-1-carboxaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.8421 84.21%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.4022 40.22%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.9178 91.78%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8961 89.61%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9350 93.50%
CYP3A4 substrate - 0.6219 62.19%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.9729 97.29%
CYP2C9 inhibition - 0.9120 91.20%
CYP2C19 inhibition - 0.9169 91.69%
CYP2D6 inhibition - 0.9559 95.59%
CYP1A2 inhibition - 0.7829 78.29%
CYP2C8 inhibition - 0.9710 97.10%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6282 62.82%
Eye corrosion + 0.8242 82.42%
Eye irritation + 0.9137 91.37%
Skin irritation + 0.8203 82.03%
Skin corrosion - 0.9524 95.24%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6072 60.72%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6190 61.90%
skin sensitisation + 0.9517 95.17%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5521 55.21%
Acute Oral Toxicity (c) IV 0.6643 66.43%
Estrogen receptor binding - 0.9697 96.97%
Androgen receptor binding - 0.7957 79.57%
Thyroid receptor binding - 0.9026 90.26%
Glucocorticoid receptor binding - 0.8186 81.86%
Aromatase binding - 0.8767 87.67%
PPAR gamma - 0.8852 88.52%
Honey bee toxicity - 0.8910 89.10%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9863 98.63%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.74% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.07% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.73% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.78% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.13% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.58% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.38% 93.56%

Cross-Links

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PubChem 12305140
NPASS NPC147723
LOTUS LTS0231554
wikiData Q104910632