Callypentayne

Details

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Internal ID 1c2c2516-54ec-48c4-a52f-657ba77dbf6e
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (12Z,18Z)-henicosa-12,18-dien-1,3,8,10,20-pentayne
SMILES (Canonical) C#CC=CCCCCC=CC#CC#CCCCC#CC#C
SMILES (Isomeric) C#C/C=C\CCCC/C=C\C#CC#CCCCC#CC#C
InChI InChI=1S/C21H20/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h1-2,5,7,17,19H,9-15H2/b7-5-,19-17-
InChI Key BZASOWOKZUQCSW-PICUFFSDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H20
Molecular Weight 272.40 g/mol
Exact Mass 272.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 4.11
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Callyberyne A
CHEMBL448827
(12Z,18Z)-henicosa-12,18-dien-1,3,8,10,20-pentayne

2D Structure

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2D Structure of Callypentayne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9755 97.55%
Caco-2 + 0.5595 55.95%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Plasma membrane 0.3413 34.13%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.8439 84.39%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8016 80.16%
P-glycoprotein inhibitior - 0.7945 79.45%
P-glycoprotein substrate - 0.9107 91.07%
CYP3A4 substrate - 0.5518 55.18%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.7542 75.42%
CYP3A4 inhibition - 0.9579 95.79%
CYP2C9 inhibition - 0.8026 80.26%
CYP2C19 inhibition - 0.8902 89.02%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.5514 55.14%
CYP2C8 inhibition - 0.8138 81.38%
CYP inhibitory promiscuity + 0.5371 53.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4258 42.58%
Eye corrosion + 0.9773 97.73%
Eye irritation - 0.6113 61.13%
Skin irritation + 0.8854 88.54%
Skin corrosion - 0.7245 72.45%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6481 64.81%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5571 55.71%
skin sensitisation + 0.8325 83.25%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.4892 48.92%
Acute Oral Toxicity (c) III 0.7611 76.11%
Estrogen receptor binding + 0.5767 57.67%
Androgen receptor binding - 0.4897 48.97%
Thyroid receptor binding + 0.6414 64.14%
Glucocorticoid receptor binding - 0.5358 53.58%
Aromatase binding - 0.5052 50.52%
PPAR gamma + 0.7747 77.47%
Honey bee toxicity - 0.8449 84.49%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.8151 81.51%

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 92.71% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.68% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.59% 96.00%
CHEMBL230 P35354 Cyclooxygenase-2 82.81% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.69% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 81.67% 95.93%

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 10778600
NPASS NPC196831
LOTUS LTS0009475
wikiData Q104950322