1-(1-Methylpyrrolidin-2-yl)-4-phenylbut-3-en-2-one

Details

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Internal ID 507c5289-7dd8-4144-a155-aef8e691c4c3
Taxonomy Alkaloids and derivatives
IUPAC Name 1-(1-methylpyrrolidin-2-yl)-4-phenylbut-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H19NO/c1-16-11-5-8-14(16)12-15(17)10-9-13-6-3-2-4-7-13/h2-4,6-7,9-10,14H,5,8,11-12H2,1H3
InChI Key CQBUTECROSOOEZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H19NO
Molecular Weight 229.32 g/mol
Exact Mass 229.146664230 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(1-Methylpyrrolidin-2-yl)-4-phenylbut-3-en-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.9001 90.01%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.4326 43.26%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9252 92.52%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior - 0.6364 63.64%
P-glycoprotein inhibitior - 0.9311 93.11%
P-glycoprotein substrate - 0.7629 76.29%
CYP3A4 substrate - 0.6072 60.72%
CYP2C9 substrate - 0.6031 60.31%
CYP2D6 substrate + 0.4321 43.21%
CYP3A4 inhibition - 0.9743 97.43%
CYP2C9 inhibition - 0.9091 90.91%
CYP2C19 inhibition + 0.5328 53.28%
CYP2D6 inhibition - 0.7285 72.85%
CYP1A2 inhibition - 0.5414 54.14%
CYP2C8 inhibition - 0.8873 88.73%
CYP inhibitory promiscuity - 0.8975 89.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6654 66.54%
Eye corrosion - 0.9704 97.04%
Eye irritation - 0.8749 87.49%
Skin irritation - 0.5514 55.14%
Skin corrosion - 0.5684 56.84%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7820 78.20%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6727 67.27%
skin sensitisation - 0.8467 84.67%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.9221 92.21%
Acute Oral Toxicity (c) III 0.5718 57.18%
Estrogen receptor binding - 0.8469 84.69%
Androgen receptor binding - 0.5544 55.44%
Thyroid receptor binding - 0.7240 72.40%
Glucocorticoid receptor binding - 0.8139 81.39%
Aromatase binding + 0.6461 64.61%
PPAR gamma - 0.6827 68.27%
Honey bee toxicity - 0.9727 97.27%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7473 74.73%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.08% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.89% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.33% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.84% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.75% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.59% 90.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.66% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.76% 95.89%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.47% 96.25%

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.
Darlingia darlingiana

Cross-Links

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PubChem 86113873
LOTUS LTS0180106
wikiData Q104967897