(3Z,18Z)-henicosa-3,18-dien-1,8,10,20-tetrayne

Details

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Internal ID 48898dd4-228a-4571-9efc-3993214fc676
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (3Z,18Z)-henicosa-3,18-dien-1,8,10,20-tetrayne
SMILES (Canonical) C#CC=CCCCCCCC#CC#CCCCC=CC#C
SMILES (Isomeric) C#C/C=C\CCCCCCC#CC#CCCC/C=C\C#C
InChI InChI=1S/C21H24/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h1-2,5-8H,9-15,17,19H2/b7-5-,8-6-
InChI Key JLMGIKDCGVHZJL-SFECMWDFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H24
Molecular Weight 276.40 g/mol
Exact Mass 276.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.80
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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Callyberyne C
CHEMBL445529
(3Z,18Z)-henicosa-3,18-dien-1,8,10,20-tetrayne

2D Structure

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2D Structure of (3Z,18Z)-henicosa-3,18-dien-1,8,10,20-tetrayne

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 + 0.5833 58.33%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.3870 38.70%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8701 87.01%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6640 66.40%
P-glycoprotein inhibitior - 0.7657 76.57%
P-glycoprotein substrate - 0.9418 94.18%
CYP3A4 substrate - 0.6094 60.94%
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 - 0.7649 76.49%
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 - 0.5694 56.94%
Skin irritation + 0.8467 84.67%
Skin corrosion - 0.8455 84.55%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6828 68.28%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6038 60.38%
skin sensitisation + 0.8308 83.08%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.4859 48.59%
Acute Oral Toxicity (c) III 0.7874 78.74%
Estrogen receptor binding + 0.6712 67.12%
Androgen receptor binding + 0.5597 55.97%
Thyroid receptor binding + 0.6340 63.40%
Glucocorticoid receptor binding - 0.5662 56.62%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7368 73.68%
Honey bee toxicity - 0.9166 91.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7900 79.00%
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 89.54% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 88.14% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.30% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.82% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.82% 91.11%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 82.20% 92.95%

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.
Corydalis turtschaninovii

Cross-Links

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PubChem 10636218
NPASS NPC62779
LOTUS LTS0016314
wikiData Q105130894