Piperolactam D

Details

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Internal ID 11fca883-c83e-4383-bf98-c0ec4224d96f
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 15-hydroxy-13,14-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one
SMILES (Canonical) COC1=C2C3=C(C4=CC=CC=C4C=C3NC2=O)C(=C1OC)O
SMILES (Isomeric) COC1=C2C3=C(C4=CC=CC=C4C=C3NC2=O)C(=C1OC)O
InChI InChI=1S/C17H13NO4/c1-21-15-13-12-10(18-17(13)20)7-8-5-3-4-6-9(8)11(12)14(19)16(15)22-2/h3-7,19H,1-2H3,(H,18,20)
InChI Key PHKYZFGDNGACRM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H13NO4
Molecular Weight 295.29 g/mol
Exact Mass 295.08445790 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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116084-93-6
1-Hydroxy-2,3-dimethoxydibenz[cd,f]indol-4(5H)-one
CHEBI:174802
DTXSID901229282
AKOS040736251
NCGC00384743-01!
1-Hydroxy-2,3-dimethoxydibenz[cd,f]indol-4(5H)-one, 9CI
10-Amino-2,3-dimethoxy-4-hydroxyphenanthrene-1-carboxylic acid lactam
15-hydroxy-13,14-dimethoxy-10-azatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(15),2,4,6,8,12(16),13-heptaen-11-one
15-hydroxy-13,14-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one

2D Structure

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2D Structure of Piperolactam D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.8677 86.77%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6344 63.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8606 86.06%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6116 61.16%
P-glycoprotein inhibitior - 0.7040 70.40%
P-glycoprotein substrate - 0.8651 86.51%
CYP3A4 substrate + 0.5974 59.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8343 83.43%
CYP3A4 inhibition - 0.6989 69.89%
CYP2C9 inhibition - 0.9103 91.03%
CYP2C19 inhibition - 0.8398 83.98%
CYP2D6 inhibition - 0.8000 80.00%
CYP1A2 inhibition + 0.8258 82.58%
CYP2C8 inhibition + 0.5826 58.26%
CYP inhibitory promiscuity + 0.5463 54.63%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4678 46.78%
Eye corrosion - 0.9935 99.35%
Eye irritation + 0.5295 52.95%
Skin irritation - 0.8534 85.34%
Skin corrosion - 0.9721 97.21%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6341 63.41%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9388 93.88%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7954 79.54%
Acute Oral Toxicity (c) III 0.4600 46.00%
Estrogen receptor binding + 0.8501 85.01%
Androgen receptor binding + 0.6683 66.83%
Thyroid receptor binding + 0.6947 69.47%
Glucocorticoid receptor binding + 0.9078 90.78%
Aromatase binding + 0.7247 72.47%
PPAR gamma + 0.7820 78.20%
Honey bee toxicity - 0.9384 93.84%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.7781 77.81%

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 99.65% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.15% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.06% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.73% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 91.71% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.01% 99.23%
CHEMBL2581 P07339 Cathepsin D 89.47% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.97% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 88.35% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.10% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.06% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.20% 94.62%
CHEMBL4208 P20618 Proteasome component C5 85.08% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.50% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.05% 99.15%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.62% 96.67%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 82.40% 81.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.11% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.02% 93.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.97% 96.09%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.59% 94.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.32% 92.62%

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.
Curcuma zedoaria
Piper attenuatum
Piper kadsura
Piper longum
Piper macropiper

Cross-Links

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PubChem 14039008
NPASS NPC294196
LOTUS LTS0255341
wikiData Q105209039