6,6-Dimethyl-2-methylidenecyclohex-3-ene-1-carbaldehyde

Details

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Internal ID bfe6b28f-de5f-40fe-b1af-9617ccfc595c
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name 6,6-dimethyl-2-methylidenecyclohex-3-ene-1-carbaldehyde
SMILES (Canonical) CC1(CC=CC(=C)C1C=O)C
SMILES (Isomeric) CC1(CC=CC(=C)C1C=O)C
InChI InChI=1S/C10H14O/c1-8-5-4-6-10(2,3)9(8)7-11/h4-5,7,9H,1,6H2,2-3H3
InChI Key HIQSWLVZAOEUPK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.34
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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33399-07-4
DTXSID50577277
HIQSWLVZAOEUPK-UHFFFAOYSA-N
2-Methylene-6,6-dimethyl-3-cyclohexene-1-carbaldehyde
2-methylene-6,6-dimethylcyclohex-3-ene-1-carboxaldehyde

2D Structure

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2D Structure of 6,6-Dimethyl-2-methylidenecyclohex-3-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 + 0.9928 99.28%
Caco-2 + 0.8599 85.99%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4515 45.15%
OATP2B1 inhibitior - 0.8644 86.44%
OATP1B1 inhibitior + 0.8788 87.88%
OATP1B3 inhibitior + 0.8925 89.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9590 95.90%
P-glycoprotein inhibitior - 0.9767 97.67%
P-glycoprotein substrate - 0.9435 94.35%
CYP3A4 substrate - 0.5343 53.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8372 83.72%
CYP3A4 inhibition - 0.7625 76.25%
CYP2C9 inhibition - 0.8329 83.29%
CYP2C19 inhibition - 0.7623 76.23%
CYP2D6 inhibition - 0.9257 92.57%
CYP1A2 inhibition - 0.8417 84.17%
CYP2C8 inhibition - 0.9585 95.85%
CYP inhibitory promiscuity - 0.6743 67.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5317 53.17%
Carcinogenicity (trinary) Non-required 0.5795 57.95%
Eye corrosion + 0.7898 78.98%
Eye irritation + 0.9232 92.32%
Skin irritation + 0.7110 71.10%
Skin corrosion - 0.8105 81.05%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7208 72.08%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.9698 96.98%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6312 63.12%
Acute Oral Toxicity (c) III 0.8399 83.99%
Estrogen receptor binding - 0.9626 96.26%
Androgen receptor binding - 0.8069 80.69%
Thyroid receptor binding - 0.7687 76.87%
Glucocorticoid receptor binding - 0.8296 82.96%
Aromatase binding - 0.7537 75.37%
PPAR gamma - 0.8613 86.13%
Honey bee toxicity - 0.8969 89.69%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9877 98.77%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.92% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 91.32% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.17% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.57% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.26% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.43% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.22% 94.80%

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.
Crocus sativus

Cross-Links

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PubChem 15715941
NPASS NPC20594