1-Pyrrol-1-ylhexadeca-2,6,8-trien-10-yn-1-one

Details

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Internal ID 1defe946-b335-4efd-87d9-005919ff6364
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles
IUPAC Name 1-pyrrol-1-ylhexadeca-2,6,8-trien-10-yn-1-one
SMILES (Canonical) CCCCCC#CC=CC=CCCC=CC(=O)N1C=CC=C1
SMILES (Isomeric) CCCCCC#CC=CC=CCCC=CC(=O)N1C=CC=C1
InChI InChI=1S/C20H25NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-20(22)21-18-15-16-19-21/h8-11,14-19H,2-5,12-13H2,1H3
InChI Key GQXSUEBJBXDGSF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H25NO
Molecular Weight 295.40 g/mol
Exact Mass 295.193614421 g/mol
Topological Polar Surface Area (TPSA) 22.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.16
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrol-1-ylhexadeca-2,6,8-trien-10-yn-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.6849 68.49%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Plasma membrane 0.5729 57.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8373 83.73%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8067 80.67%
BSEP inhibitior - 0.5412 54.12%
P-glycoprotein inhibitior - 0.6540 65.40%
P-glycoprotein substrate - 0.7858 78.58%
CYP3A4 substrate + 0.5179 51.79%
CYP2C9 substrate + 0.8002 80.02%
CYP2D6 substrate - 0.8832 88.32%
CYP3A4 inhibition - 0.8198 81.98%
CYP2C9 inhibition + 0.5402 54.02%
CYP2C19 inhibition + 0.6420 64.20%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition + 0.6168 61.68%
CYP2C8 inhibition - 0.6334 63.34%
CYP inhibitory promiscuity + 0.7139 71.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.4560 45.60%
Eye corrosion - 0.8159 81.59%
Eye irritation - 0.9154 91.54%
Skin irritation - 0.5330 53.30%
Skin corrosion - 0.7480 74.80%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7401 74.01%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6304 63.04%
skin sensitisation - 0.8163 81.63%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5632 56.32%
Mitochondrial toxicity + 0.5587 55.87%
Nephrotoxicity + 0.6808 68.08%
Acute Oral Toxicity (c) III 0.6806 68.06%
Estrogen receptor binding + 0.7315 73.15%
Androgen receptor binding + 0.7194 71.94%
Thyroid receptor binding + 0.7320 73.20%
Glucocorticoid receptor binding - 0.6273 62.73%
Aromatase binding + 0.7421 74.21%
PPAR gamma + 0.6980 69.80%
Honey bee toxicity - 0.9487 94.87%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7253 72.53%
Fish aquatic toxicity + 0.8796 87.96%

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
CHEMBL230 P35354 Cyclooxygenase-2 97.56% 89.63%
CHEMBL2581 P07339 Cathepsin D 95.60% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 93.49% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.22% 99.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.87% 85.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.40% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.06% 92.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.65% 97.25%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.49% 92.86%
CHEMBL1781 P11387 DNA topoisomerase I 81.16% 97.00%

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.
Achillea ageratifolia

Cross-Links

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PubChem 162909327
LOTUS LTS0039150
wikiData Q105015607