N-Methyl Piperolactam A

Details

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Internal ID b5ed7826-bfb9-49fd-a687-f957335aba14
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 15-hydroxy-14-methoxy-10-methyl-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H13NO3/c1-18-12-7-9-5-3-4-6-10(9)15-14(12)11(17(18)20)8-13(21-2)16(15)19/h3-8,19H,1-2H3
InChI Key SXOOWJJLSWDXTQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H13NO3
Molecular Weight 279.29 g/mol
Exact Mass 279.08954328 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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15-hydroxy-14-methoxy-10-methyl-10-azatetracyclo(7.6.1.02,7.012,16)hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one
15-hydroxy-14-methoxy-10-methyl-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one
RefChem:163670
CHEMBL505869

2D Structure

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2D Structure of N-Methyl Piperolactam A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 + 0.8391 83.91%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.6478 64.78%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.8693 86.93%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8564 85.64%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7504 75.04%
P-glycoprotein substrate - 0.7081 70.81%
CYP3A4 substrate + 0.5746 57.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8171 81.71%
CYP3A4 inhibition - 0.6230 62.30%
CYP2C9 inhibition - 0.7530 75.30%
CYP2C19 inhibition - 0.5625 56.25%
CYP2D6 inhibition - 0.8888 88.88%
CYP1A2 inhibition + 0.9313 93.13%
CYP2C8 inhibition + 0.4681 46.81%
CYP inhibitory promiscuity + 0.7211 72.11%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Warning 0.3758 37.58%
Eye corrosion - 0.9895 98.95%
Eye irritation + 0.6282 62.82%
Skin irritation - 0.7937 79.37%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7109 71.09%
Micronuclear + 0.7859 78.59%
Hepatotoxicity + 0.6304 63.04%
skin sensitisation - 0.9248 92.48%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6701 67.01%
Nephrotoxicity - 0.8199 81.99%
Acute Oral Toxicity (c) III 0.5148 51.48%
Estrogen receptor binding + 0.8842 88.42%
Androgen receptor binding + 0.6400 64.00%
Thyroid receptor binding + 0.6706 67.06%
Glucocorticoid receptor binding + 0.9406 94.06%
Aromatase binding + 0.7774 77.74%
PPAR gamma + 0.6439 64.39%
Honey bee toxicity - 0.9372 93.72%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.8412 84.12%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.96% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.84% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.72% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.47% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.86% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.89% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.39% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.62% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.77% 85.14%
CHEMBL1255126 O15151 Protein Mdm4 85.72% 90.20%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.42% 96.67%
CHEMBL2056 P21728 Dopamine D1 receptor 85.18% 91.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.13% 94.75%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.32% 80.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.13% 89.00%
CHEMBL4208 P20618 Proteasome component C5 82.37% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.61% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.47% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.01% 99.15%

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.
Dalbergia louvelii
Piper ribesioides

Cross-Links

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PubChem 25264744
NPASS NPC207873
ChEMBL CHEMBL505869
LOTUS LTS0037768
wikiData Q105263241