(Z)-henicos-3-en-1,8,20-triyne

Details

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Internal ID 86755dc8-395a-4286-89b1-1054935c9664
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (Z)-henicos-3-en-1,8,20-triyne
SMILES (Canonical) C#CCCCCCCCCCCC#CCCCC=CC#C
SMILES (Isomeric) C#CCCCCCCCCCCC#CCCC/C=C\C#C
InChI InChI=1S/C21H30/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h1-2,5,7H,6,8-14,16,18-21H2/b7-5-
InChI Key ODOHBJISRZXRAM-ALCCZGGFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H30
Molecular Weight 282.50 g/mol
Exact Mass 282.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.90
Atomic LogP (AlogP) 5.88
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-henicos-3-en-1,8,20-triyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.6276 62.76%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Plasma membrane 0.3870 38.70%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.8805 88.05%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5776 57.76%
P-glycoprotein inhibitior - 0.8133 81.33%
P-glycoprotein substrate - 0.9508 95.08%
CYP3A4 substrate - 0.5973 59.73%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.7542 75.42%
CYP3A4 inhibition - 0.9708 97.08%
CYP2C9 inhibition - 0.7984 79.84%
CYP2C19 inhibition - 0.8958 89.58%
CYP2D6 inhibition - 0.9624 96.24%
CYP1A2 inhibition - 0.5591 55.91%
CYP2C8 inhibition - 0.8360 83.60%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5500 55.00%
Carcinogenicity (trinary) Warning 0.4130 41.30%
Eye corrosion + 0.9782 97.82%
Eye irritation - 0.6347 63.47%
Skin irritation + 0.8467 84.67%
Skin corrosion - 0.8455 84.55%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3720 37.20%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5913 59.13%
skin sensitisation + 0.8308 83.08%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5558 55.58%
Acute Oral Toxicity (c) III 0.7874 78.74%
Estrogen receptor binding + 0.6521 65.21%
Androgen receptor binding - 0.7210 72.10%
Thyroid receptor binding + 0.6494 64.94%
Glucocorticoid receptor binding - 0.6092 60.92%
Aromatase binding + 0.6103 61.03%
PPAR gamma + 0.5574 55.74%
Honey bee toxicity - 0.9240 92.40%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9083 90.83%

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
CHEMBL221 P23219 Cyclooxygenase-1 91.84% 90.17%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 89.04% 92.95%
CHEMBL230 P35354 Cyclooxygenase-2 88.11% 89.63%
CHEMBL2039 P27338 Monoamine oxidase B 85.96% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.80% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.58% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.35% 96.00%

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.
There are no matching plants.

Cross-Links

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PubChem 10850502
LOTUS LTS0230777
wikiData Q105189954