(S)-2,6-Dimethyl-5-heptenal

Details

Top
Internal ID f153d95b-fb40-442a-a5f0-05814a248f91
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2S)-2,6-dimethylhept-5-enal
SMILES (Canonical) CC(CCC=C(C)C)C=O
SMILES (Isomeric) C[C@@H](CCC=C(C)C)C=O
InChI InChI=1S/C9H16O/c1-8(2)5-4-6-9(3)7-10/h5,7,9H,4,6H2,1-3H3/t9-/m0/s1
InChI Key YGFGZTXGYTUXBA-VIFPVBQESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C9H16O
Molecular Weight 140.22 g/mol
Exact Mass 140.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
SCHEMBL17242080
(S)-2,6-Dimethyl-5-heptenal
(s)-(+)-2,6-dimethyl-5-heptenal

2D Structure

Top
2D Structure of (S)-2,6-Dimethyl-5-heptenal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.7557 75.57%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Nucleus 0.7403 74.03%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9083 90.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8710 87.10%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9574 95.74%
CYP3A4 substrate - 0.6933 69.33%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.7942 79.42%
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 - 0.9974 99.74%
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 + 0.8872 88.72%
Skin irritation + 0.9349 93.49%
Skin corrosion + 0.5099 50.99%
Ames mutagenesis - 0.6678 66.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7478 74.78%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6025 60.25%
skin sensitisation + 0.9561 95.61%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7030 70.30%
Acute Oral Toxicity (c) III 0.8232 82.32%
Estrogen receptor binding - 0.9763 97.63%
Androgen receptor binding - 0.8780 87.80%
Thyroid receptor binding - 0.8908 89.08%
Glucocorticoid receptor binding - 0.8923 89.23%
Aromatase binding - 0.9070 90.70%
PPAR gamma - 0.8448 84.48%
Honey bee toxicity - 0.8890 88.90%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.8987 89.87%

Targets

Top

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 91.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.19% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.74% 89.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.37% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 82.62% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.20% 90.71%

Plants that contains it

Top
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.
Hypericum perforatum

Cross-Links

Top
PubChem 6994791
NPASS NPC157156