(4S)-3,3,4-trimethylcyclohexene-1-carbaldehyde

Details

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Internal ID d8e7f75a-4942-4d6f-b6ad-a896bf8abf13
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name (4S)-3,3,4-trimethylcyclohexene-1-carbaldehyde
SMILES (Canonical) CC1CCC(=CC1(C)C)C=O
SMILES (Isomeric) C[C@H]1CCC(=CC1(C)C)C=O
InChI InChI=1S/C10H16O/c1-8-4-5-9(7-11)6-10(8,2)3/h6-8H,4-5H2,1-3H3/t8-/m0/s1
InChI Key ANWGQUDDFBXFAP-QMMMGPOBSA-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 2.80
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S)-3,3,4-trimethylcyclohexene-1-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.8904 89.04%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.5032 50.32%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9126 91.26%
OATP1B3 inhibitior - 0.3150 31.50%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8965 89.65%
P-glycoprotein inhibitior - 0.9806 98.06%
P-glycoprotein substrate - 0.9473 94.73%
CYP3A4 substrate - 0.5764 57.64%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8245 82.45%
CYP3A4 inhibition - 0.9366 93.66%
CYP2C9 inhibition - 0.8955 89.55%
CYP2C19 inhibition - 0.8570 85.70%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.8088 80.88%
CYP2C8 inhibition - 0.9593 95.93%
CYP inhibitory promiscuity - 0.7087 70.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5466 54.66%
Eye corrosion - 0.8472 84.72%
Eye irritation + 0.6365 63.65%
Skin irritation + 0.8615 86.15%
Skin corrosion - 0.9155 91.55%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5954 59.54%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.9335 93.35%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5528 55.28%
Acute Oral Toxicity (c) III 0.8690 86.90%
Estrogen receptor binding - 0.8840 88.40%
Androgen receptor binding - 0.8015 80.15%
Thyroid receptor binding - 0.8448 84.48%
Glucocorticoid receptor binding - 0.9129 91.29%
Aromatase binding - 0.9238 92.38%
PPAR gamma - 0.8769 87.69%
Honey bee toxicity - 0.9284 92.84%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9787 97.87%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.16% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.90% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.55% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.88% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.41% 97.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.27% 93.40%
CHEMBL2581 P07339 Cathepsin D 83.75% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.46% 97.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163040247
LOTUS LTS0205546
wikiData Q104915476