2,6-Dimethyl-2-heptenal

Details

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Internal ID 3f01c3a2-1f05-479e-8e9e-0ca8364594d3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (E)-2,6-dimethylhept-2-enal
SMILES (Canonical) CC(C)CCC=C(C)C=O
SMILES (Isomeric) CC(C)CC/C=C(\C)/C=O
InChI InChI=1S/C9H16O/c1-8(2)5-4-6-9(3)7-10/h6-8H,4-5H2,1-3H3/b9-6+
InChI Key YXVDCUSVRUNXEM-RMKNXTFCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O
Molecular Weight 140.22 g/mol
Exact Mass 140.120115130 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 4

Synonyms

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2,6,6-Trimethyl-2-hexenal
SCHEMBL1783297
YXVDCUSVRUNXEM-RMKNXTFCSA-N

2D Structure

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2D Structure of 2,6-Dimethyl-2-heptenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.8620 86.20%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Nucleus 0.7403 74.03%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9083 90.83%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8910 89.10%
P-glycoprotein inhibitior - 0.9859 98.59%
P-glycoprotein substrate - 0.9138 91.38%
CYP3A4 substrate - 0.6568 65.68%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.9851 98.51%
CYP2C9 inhibition - 0.9265 92.65%
CYP2C19 inhibition - 0.9229 92.29%
CYP2D6 inhibition - 0.9534 95.34%
CYP1A2 inhibition - 0.7287 72.87%
CYP2C8 inhibition - 0.9968 99.68%
CYP inhibitory promiscuity - 0.7571 75.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5545 55.45%
Eye corrosion + 0.8157 81.57%
Eye irritation + 0.9380 93.80%
Skin irritation + 0.9349 93.49%
Skin corrosion + 0.5099 50.99%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6520 65.20%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.9561 95.61%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5158 51.58%
Acute Oral Toxicity (c) III 0.8232 82.32%
Estrogen receptor binding - 0.9860 98.60%
Androgen receptor binding - 0.9298 92.98%
Thyroid receptor binding - 0.8899 88.99%
Glucocorticoid receptor binding - 0.8951 89.51%
Aromatase binding - 0.8975 89.75%
PPAR gamma - 0.9009 90.09%
Honey bee toxicity - 0.9120 91.20%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.8987 89.87%

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
CHEMBL2581 P07339 Cathepsin D 91.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.64% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.09% 89.34%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.81% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.32% 99.17%

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.
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 5352222
NPASS NPC158383