Capillin

Details

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Internal ID 3a75b551-c36e-48d8-a4d2-f95057d56b89
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 1-phenylhexa-2,4-diyn-1-one
SMILES (Canonical) CC#CC#CC(=O)C1=CC=CC=C1
SMILES (Isomeric) CC#CC#CC(=O)C1=CC=CC=C1
InChI InChI=1S/C12H8O/c1-2-3-5-10-12(13)11-8-6-4-7-9-11/h4,6-9H,1H3
InChI Key RAZOKRUZEQERLH-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C12H8O
Molecular Weight 168.19 g/mol
Exact Mass 168.057514874 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 1.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1-phenylhexa-2,4-diyn-1-one
495-74-9
2,4-HEXADIYNOPHENONE
2,4-Hexadiyn-1-one, 1-phenyl-
1-Phenyl-2,4-hexadiyn-1-one
9JXZ3SJG0I
NSC 113499
BRN 1865168
NSC-113499
2, 4-Hexadiynophenone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Capillin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.9131 91.31%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6799 67.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9741 97.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9051 90.51%
P-glycoprotein inhibitior - 0.9743 97.43%
P-glycoprotein substrate - 0.9565 95.65%
CYP3A4 substrate - 0.7179 71.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7717 77.17%
CYP3A4 inhibition - 0.9498 94.98%
CYP2C9 inhibition - 0.9235 92.35%
CYP2C19 inhibition - 0.8995 89.95%
CYP2D6 inhibition - 0.9727 97.27%
CYP1A2 inhibition + 0.5950 59.50%
CYP2C8 inhibition - 0.8857 88.57%
CYP inhibitory promiscuity - 0.7409 74.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5264 52.64%
Carcinogenicity (trinary) Non-required 0.6074 60.74%
Eye corrosion + 0.9796 97.96%
Eye irritation + 0.9728 97.28%
Skin irritation + 0.9268 92.68%
Skin corrosion - 0.5069 50.69%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8416 84.16%
Micronuclear - 0.7041 70.41%
Hepatotoxicity + 0.6597 65.97%
skin sensitisation + 0.9089 90.89%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6067 60.67%
Acute Oral Toxicity (c) III 0.6389 63.89%
Estrogen receptor binding - 0.8545 85.45%
Androgen receptor binding - 0.7304 73.04%
Thyroid receptor binding - 0.7663 76.63%
Glucocorticoid receptor binding - 0.7680 76.80%
Aromatase binding - 0.6157 61.57%
PPAR gamma - 0.8213 82.13%
Honey bee toxicity - 0.9776 97.76%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.6853 68.53%

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 95.46% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.37% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.86% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.85% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.78% 94.62%
CHEMBL2535 P11166 Glucose transporter 83.07% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.41% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.11% 99.17%

Cross-Links

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PubChem 10321
NPASS NPC180968
LOTUS LTS0102435
wikiData Q18012475