2,2-Dimethyl-3-(4-methyl-7-oxooct-3-enyl)cyclopropane-1-carbaldehyde

Details

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Internal ID 6d16f5e1-47c2-453e-8aff-b036a637aa06
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 2,2-dimethyl-3-(4-methyl-7-oxooct-3-enyl)cyclopropane-1-carbaldehyde
SMILES (Canonical) CC(=CCCC1C(C1(C)C)C=O)CCC(=O)C
SMILES (Isomeric) CC(=CCCC1C(C1(C)C)C=O)CCC(=O)C
InChI InChI=1S/C15H24O2/c1-11(8-9-12(2)17)6-5-7-13-14(10-16)15(13,3)4/h6,10,13-14H,5,7-9H2,1-4H3
InChI Key DFFNANWUVIXRPP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,2-Dimethyl-3-(4-methyl-7-oxooct-3-enyl)cyclopropane-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 + 0.9920 99.20%
Caco-2 + 0.6132 61.32%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6315 63.15%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.8855 88.55%
OATP1B3 inhibitior + 0.8805 88.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6344 63.44%
P-glycoprotein inhibitior - 0.9010 90.10%
P-glycoprotein substrate - 0.8992 89.92%
CYP3A4 substrate - 0.5192 51.92%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8099 80.99%
CYP3A4 inhibition - 0.8454 84.54%
CYP2C9 inhibition - 0.8127 81.27%
CYP2C19 inhibition - 0.7504 75.04%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.6311 63.11%
CYP2C8 inhibition - 0.8876 88.76%
CYP inhibitory promiscuity - 0.7546 75.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5917 59.17%
Eye corrosion - 0.8863 88.63%
Eye irritation - 0.7906 79.06%
Skin irritation + 0.6098 60.98%
Skin corrosion - 0.9787 97.87%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation + 0.8869 88.69%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.7386 73.86%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4512 45.12%
Acute Oral Toxicity (c) III 0.6855 68.55%
Estrogen receptor binding - 0.7646 76.46%
Androgen receptor binding - 0.7803 78.03%
Thyroid receptor binding - 0.6272 62.72%
Glucocorticoid receptor binding - 0.5093 50.93%
Aromatase binding - 0.7191 71.91%
PPAR gamma - 0.4935 49.35%
Honey bee toxicity - 0.8018 80.18%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9731 97.31%

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 94.68% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.37% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 86.40% 90.17%
CHEMBL340 P08684 Cytochrome P450 3A4 86.15% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.11% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.65% 99.17%

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 72738640
LOTUS LTS0181024
wikiData Q104977841