(1R,5S)-2,5,6,6-tetramethylcyclohex-2-ene-1-carbaldehyde

Details

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Internal ID 406e0a33-6831-4e52-b7fc-9cae574a28ed
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name (1R,5S)-2,5,6,6-tetramethylcyclohex-2-ene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H18O/c1-8-5-6-9(2)11(3,4)10(8)7-12/h5,7,9-10H,6H2,1-4H3/t9-,10+/m0/s1
InChI Key BTFBPMQRSSBITM-VHSXEESVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O
Molecular Weight 166.26 g/mol
Exact Mass 166.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.81
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 (1R,5S)-2,5,6,6-tetramethylcyclohex-2-ene-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 + 0.9959 99.59%
Caco-2 + 0.7564 75.64%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4533 45.33%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.9208 92.08%
OATP1B3 inhibitior + 0.8569 85.69%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8827 88.27%
P-glycoprotein inhibitior - 0.9466 94.66%
P-glycoprotein substrate - 0.9390 93.90%
CYP3A4 substrate - 0.5747 57.47%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8100 81.00%
CYP3A4 inhibition - 0.8589 85.89%
CYP2C9 inhibition - 0.8692 86.92%
CYP2C19 inhibition - 0.8063 80.63%
CYP2D6 inhibition - 0.9232 92.32%
CYP1A2 inhibition - 0.8343 83.43%
CYP2C8 inhibition - 0.9636 96.36%
CYP inhibitory promiscuity - 0.6278 62.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5617 56.17%
Carcinogenicity (trinary) Non-required 0.5777 57.77%
Eye corrosion + 0.4790 47.90%
Eye irritation + 0.7531 75.31%
Skin irritation + 0.8400 84.00%
Skin corrosion - 0.7547 75.47%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6084 60.84%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6448 64.48%
skin sensitisation + 0.9547 95.47%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.4804 48.04%
Acute Oral Toxicity (c) III 0.8293 82.93%
Estrogen receptor binding - 0.8700 87.00%
Androgen receptor binding - 0.6893 68.93%
Thyroid receptor binding - 0.8573 85.73%
Glucocorticoid receptor binding - 0.9352 93.52%
Aromatase binding - 0.8650 86.50%
PPAR gamma - 0.8652 86.52%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9869 98.69%

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 91.15% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.06% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.98% 86.00%
CHEMBL1871 P10275 Androgen Receptor 85.05% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.23% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.07% 100.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.04% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.51% 86.33%

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 14432941
LOTUS LTS0255072
wikiData Q104945568