Piperdardine

Details

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Internal ID 499c75cf-e9c1-4714-aae3-19a19b4bc287
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name (2E,4E)-7-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylhepta-2,4-dien-1-one
SMILES (Canonical) C1CCN(CC1)C(=O)C=CC=CCCC2=CC3=C(C=C2)OCO3
SMILES (Isomeric) C1CCN(CC1)C(=O)/C=C/C=C/CCC2=CC3=C(C=C2)OCO3
InChI InChI=1S/C19H23NO3/c21-19(20-12-6-3-7-13-20)9-5-2-1-4-8-16-10-11-17-18(14-16)23-15-22-17/h1-2,5,9-11,14H,3-4,6-8,12-13,15H2/b2-1+,9-5+
InChI Key FNECAUUPWFQEGF-RPFQBYKKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO3
Molecular Weight 313.40 g/mol
Exact Mass 313.16779360 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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SCHEMBL15471330
SCHEMBL17073998
AKOS040735490

2D Structure

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2D Structure of Piperdardine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.8160 81.60%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7406 74.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9336 93.36%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7930 79.30%
P-glycoprotein inhibitior + 0.7623 76.23%
P-glycoprotein substrate - 0.8123 81.23%
CYP3A4 substrate - 0.5148 51.48%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition + 0.7018 70.18%
CYP2C9 inhibition - 0.8788 87.88%
CYP2C19 inhibition - 0.6068 60.68%
CYP2D6 inhibition + 0.8288 82.88%
CYP1A2 inhibition + 0.8777 87.77%
CYP2C8 inhibition - 0.8108 81.08%
CYP inhibitory promiscuity + 0.8272 82.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5932 59.32%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.6620 66.20%
Skin irritation - 0.7307 73.07%
Skin corrosion - 0.8626 86.26%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4812 48.12%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8192 81.92%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.8199 81.99%
Acute Oral Toxicity (c) III 0.8109 81.09%
Estrogen receptor binding + 0.7486 74.86%
Androgen receptor binding + 0.8464 84.64%
Thyroid receptor binding + 0.5345 53.45%
Glucocorticoid receptor binding - 0.5237 52.37%
Aromatase binding + 0.6443 64.43%
PPAR gamma + 0.5810 58.10%
Honey bee toxicity - 0.9219 92.19%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5652 56.52%
Fish aquatic toxicity + 0.8457 84.57%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 98.27% 83.57%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.67% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.26% 96.77%
CHEMBL2581 P07339 Cathepsin D 94.55% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.95% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.49% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.16% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.14% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.57% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.52% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.49% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.99% 94.80%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.44% 96.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.45% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.57% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.24% 96.00%

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.
Piper longum
Piper nigrum
Piper sintenense
Piper tuberculatum

Cross-Links

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PubChem 10086948
NPASS NPC281915
LOTUS LTS0013945
wikiData Q104998246