(3E,5E)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexa-3,5-dien-2-one

Details

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Internal ID 286ed409-f56f-484f-b803-d61d7a9315eb
Taxonomy Alkaloids and derivatives
IUPAC Name (3E,5E)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexa-3,5-dien-2-one
SMILES (Canonical) CN1CCCC1CC(=O)C=CC=CC2=CC=CC=C2
SMILES (Isomeric) CN1CCC[C@@H]1CC(=O)/C=C/C=C/C2=CC=CC=C2
InChI InChI=1S/C17H21NO/c1-18-13-7-11-16(18)14-17(19)12-6-5-10-15-8-3-2-4-9-15/h2-6,8-10,12,16H,7,11,13-14H2,1H3/b10-5+,12-6+/t16-/m1/s1
InChI Key PEYDJQPYPIFSAO-OHXLYVNLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H21NO
Molecular Weight 255.35 g/mol
Exact Mass 255.162314293 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,5E)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexa-3,5-dien-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 + 0.8851 88.51%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.4326 43.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9099 90.99%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior + 0.6378 63.78%
P-glycoprotein inhibitior - 0.8578 85.78%
P-glycoprotein substrate - 0.7111 71.11%
CYP3A4 substrate - 0.5454 54.54%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate + 0.3647 36.47%
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 - 0.8529 85.29%
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 - 0.9126 91.26%
Skin irritation - 0.5514 55.14%
Skin corrosion - 0.5684 56.84%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7230 72.30%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5416 54.16%
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 - 0.9172 91.72%
Acute Oral Toxicity (c) III 0.5718 57.18%
Estrogen receptor binding + 0.5497 54.97%
Androgen receptor binding - 0.7049 70.49%
Thyroid receptor binding - 0.7408 74.08%
Glucocorticoid receptor binding - 0.8440 84.40%
Aromatase binding + 0.6377 63.77%
PPAR gamma - 0.5708 57.08%
Honey bee toxicity - 0.9709 97.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.20% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.98% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.40% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.58% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.77% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.56% 96.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.93% 93.00%
CHEMBL4208 P20618 Proteasome component C5 82.75% 90.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.31% 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.
Bombax ceiba
Darlingia darlingiana
Pachira aquatica

Cross-Links

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PubChem 163186899
LOTUS LTS0273702
wikiData Q105353262