(Z)-1-pyrrol-1-ylhexadec-7-en-10-yn-1-one

Details

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Internal ID 59b46e4b-86ae-4d92-8a2f-de5c420732a6
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles
IUPAC Name (Z)-1-pyrrol-1-ylhexadec-7-en-10-yn-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H29NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-20(22)21-18-15-16-19-21/h9-10,15-16,18-19H,2-5,8,11-14,17H2,1H3/b10-9-
InChI Key ZFTGBFIOZBPMEU-KTKRTIGZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H29NO
Molecular Weight 299.40 g/mol
Exact Mass 299.224914549 g/mol
Topological Polar Surface Area (TPSA) 22.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.61
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-1-pyrrol-1-ylhexadec-7-en-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 + 0.9948 99.48%
Caco-2 + 0.6525 65.25%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Plasma membrane 0.6437 64.37%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.7246 72.46%
OATP1B3 inhibitior + 0.9402 94.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.4862 48.62%
P-glycoprotein inhibitior - 0.7031 70.31%
P-glycoprotein substrate - 0.8073 80.73%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate + 0.6007 60.07%
CYP2D6 substrate - 0.8594 85.94%
CYP3A4 inhibition - 0.7476 74.76%
CYP2C9 inhibition - 0.5233 52.33%
CYP2C19 inhibition + 0.7549 75.49%
CYP2D6 inhibition - 0.8966 89.66%
CYP1A2 inhibition - 0.5119 51.19%
CYP2C8 inhibition + 0.4775 47.75%
CYP inhibitory promiscuity + 0.6473 64.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5776 57.76%
Eye corrosion - 0.8792 87.92%
Eye irritation - 0.9231 92.31%
Skin irritation - 0.5763 57.63%
Skin corrosion - 0.6957 69.57%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7746 77.46%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5658 56.58%
skin sensitisation - 0.8683 86.83%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.5855 58.55%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.5676 56.76%
Acute Oral Toxicity (c) III 0.6026 60.26%
Estrogen receptor binding + 0.7327 73.27%
Androgen receptor binding + 0.5285 52.85%
Thyroid receptor binding + 0.7085 70.85%
Glucocorticoid receptor binding - 0.6896 68.96%
Aromatase binding - 0.5113 51.13%
PPAR gamma + 0.8562 85.62%
Honey bee toxicity - 0.9658 96.58%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8378 83.78%
Fish aquatic toxicity + 0.8559 85.59%

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 98.81% 89.63%
CHEMBL2581 P07339 Cathepsin D 97.89% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.86% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.99% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.65% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 88.47% 97.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.08% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 84.32% 90.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.11% 92.86%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.21% 97.21%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.76% 91.81%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.85% 96.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.53% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.47% 93.56%

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 13846808
LOTUS LTS0116171
wikiData Q105374671