6-Methylhept-5-enal

Details

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Internal ID 164032ac-f798-482d-b400-67de6c023b5d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name 6-methylhept-5-enal
SMILES (Canonical) CC(=CCCCC=O)C
SMILES (Isomeric) CC(=CCCCC=O)C
InChI InChI=1S/C8H14O/c1-8(2)6-4-3-5-7-9/h6-7H,3-5H2,1-2H3
InChI Key GUIZUDCRTPIDCW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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SCHEMBL10885356

2D Structure

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2D Structure of 6-Methylhept-5-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.8767 87.67%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Nucleus 0.4214 42.14%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9015 90.15%
OATP1B3 inhibitior + 0.9287 92.87%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9022 90.22%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9433 94.33%
CYP3A4 substrate - 0.6503 65.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7873 78.73%
CYP3A4 inhibition - 0.9758 97.58%
CYP2C9 inhibition - 0.9350 93.50%
CYP2C19 inhibition - 0.9233 92.33%
CYP2D6 inhibition - 0.9515 95.15%
CYP1A2 inhibition - 0.7175 71.75%
CYP2C8 inhibition - 0.9920 99.20%
CYP inhibitory promiscuity - 0.7894 78.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6367 63.67%
Eye corrosion + 0.9146 91.46%
Eye irritation + 0.9797 97.97%
Skin irritation + 0.9244 92.44%
Skin corrosion + 0.5482 54.82%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7188 71.88%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9284 92.84%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.7284 72.84%
Acute Oral Toxicity (c) III 0.7911 79.11%
Estrogen receptor binding - 0.9640 96.40%
Androgen receptor binding - 0.9326 93.26%
Thyroid receptor binding - 0.9017 90.17%
Glucocorticoid receptor binding - 0.8958 89.58%
Aromatase binding - 0.8516 85.16%
PPAR gamma - 0.7947 79.47%
Honey bee toxicity - 0.9512 95.12%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.6442 64.42%

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 88.64% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.38% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 85.78% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.34% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.71% 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.
Cleistopholis patens

Cross-Links

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PubChem 11586306
LOTUS LTS0169611
wikiData Q105020190