Methyl 7-cyanohept-2-en-4,6-diynoate

Details

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Internal ID da2fc3eb-349b-4a4c-9fa7-de6b4b7eecec
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl 7-cyanohept-2-en-4,6-diynoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H5NO2/c1-12-9(11)7-5-3-2-4-6-8-10/h5,7H,1H3
InChI Key GGFQWVHFZCYUGM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H5NO2
Molecular Weight 159.14 g/mol
Exact Mass 159.032028402 g/mol
Topological Polar Surface Area (TPSA) 50.10 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.25
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 7-cyanohept-2-en-4,6-diynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 - 0.5719 57.19%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5618 56.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9236 92.36%
P-glycoprotein inhibitior - 0.9760 97.60%
P-glycoprotein substrate - 0.9506 95.06%
CYP3A4 substrate - 0.5351 53.51%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8711 87.11%
CYP3A4 inhibition - 0.9474 94.74%
CYP2C9 inhibition - 0.8668 86.68%
CYP2C19 inhibition - 0.9205 92.05%
CYP2D6 inhibition - 0.9692 96.92%
CYP1A2 inhibition - 0.6889 68.89%
CYP2C8 inhibition - 0.9272 92.72%
CYP inhibitory promiscuity - 0.8399 83.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6444 64.44%
Carcinogenicity (trinary) Non-required 0.6462 64.62%
Eye corrosion + 0.9634 96.34%
Eye irritation + 0.9515 95.15%
Skin irritation + 0.7398 73.98%
Skin corrosion + 0.9542 95.42%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6466 64.66%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5678 56.78%
skin sensitisation + 0.6523 65.23%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.7832 78.32%
Acute Oral Toxicity (c) II 0.7359 73.59%
Estrogen receptor binding - 0.8777 87.77%
Androgen receptor binding - 0.7965 79.65%
Thyroid receptor binding - 0.7380 73.80%
Glucocorticoid receptor binding - 0.7213 72.13%
Aromatase binding - 0.6832 68.32%
PPAR gamma - 0.7997 79.97%
Honey bee toxicity - 0.6208 62.08%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.5430 54.30%

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 90.61% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.86% 91.11%
CHEMBL1871 P10275 Androgen Receptor 81.14% 96.43%
CHEMBL4040 P28482 MAP kinase ERK2 80.96% 83.82%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.83% 96.00%

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 73797384
LOTUS LTS0223128
wikiData Q105008015