1-Pyrrol-1-ylhexadeca-2,7-dien-10-yn-1-one

Details

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Internal ID 72e322a2-c6e4-4cf6-a904-87c4ca9cfb14
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles
IUPAC Name 1-pyrrol-1-ylhexadeca-2,7-dien-10-yn-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H27NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-20(22)21-18-15-16-19-21/h9-10,14-19H,2-5,8,11-13H2,1H3
InChI Key DPEZRVODGRVDEX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H27NO
Molecular Weight 297.40 g/mol
Exact Mass 297.209264485 g/mol
Topological Polar Surface Area (TPSA) 22.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.38
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrol-1-ylhexadeca-2,7-dien-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 + 0.9916 99.16%
Caco-2 + 0.6666 66.66%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5907 59.07%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.7836 78.36%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5068 50.68%
P-glycoprotein inhibitior - 0.6973 69.73%
P-glycoprotein substrate - 0.7830 78.30%
CYP3A4 substrate + 0.5051 50.51%
CYP2C9 substrate + 0.8003 80.03%
CYP2D6 substrate - 0.8875 88.75%
CYP3A4 inhibition - 0.7295 72.95%
CYP2C9 inhibition + 0.5499 54.99%
CYP2C19 inhibition + 0.6857 68.57%
CYP2D6 inhibition - 0.9085 90.85%
CYP1A2 inhibition + 0.5969 59.69%
CYP2C8 inhibition + 0.5227 52.27%
CYP inhibitory promiscuity + 0.7427 74.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.4914 49.14%
Eye corrosion - 0.8165 81.65%
Eye irritation - 0.8853 88.53%
Skin irritation - 0.5509 55.09%
Skin corrosion - 0.7568 75.68%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7281 72.81%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5304 53.04%
skin sensitisation - 0.8315 83.15%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5521 55.21%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5671 56.71%
Acute Oral Toxicity (c) III 0.6552 65.52%
Estrogen receptor binding + 0.7930 79.30%
Androgen receptor binding + 0.6532 65.32%
Thyroid receptor binding + 0.8031 80.31%
Glucocorticoid receptor binding - 0.6073 60.73%
Aromatase binding + 0.6773 67.73%
PPAR gamma + 0.8772 87.72%
Honey bee toxicity - 0.9725 97.25%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6413 64.13%
Fish aquatic toxicity + 0.9409 94.09%

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
CHEMBL2581 P07339 Cathepsin D 96.06% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 94.95% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.89% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.80% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.82% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 86.81% 90.17%
CHEMBL1781 P11387 DNA topoisomerase I 84.63% 97.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.19% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.66% 96.95%

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.
Achillea ageratifolia

Cross-Links

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PubChem 162842862
LOTUS LTS0255315
wikiData Q104986468