Polyandrocarpamide B

Details

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Internal ID 59f77580-4251-4ee5-958f-2fc2941db89f
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name N-[2-(4-hydroxy-3-iodophenyl)ethyl]-2-(1H-indol-3-yl)-2-oxoacetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H15IN2O3/c19-14-9-11(5-6-16(14)22)7-8-20-18(24)17(23)13-10-21-15-4-2-1-3-12(13)15/h1-6,9-10,21-22H,7-8H2,(H,20,24)
InChI Key LYSQOZZYHKCETK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H15IN2O3
Molecular Weight 434.20 g/mol
Exact Mass 434.01274 g/mol
Topological Polar Surface Area (TPSA) 82.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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DTXSID10156148
1H-Indole-3-acetamide, N-(2-(4-hydroxy-3-iodophenyl)ethyl)-alpha-oxo-

2D Structure

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2D Structure of Polyandrocarpamide B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 - 0.7478 74.78%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7567 75.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8645 86.45%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.8409 84.09%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7330 73.30%
P-glycoprotein inhibitior - 0.7564 75.64%
P-glycoprotein substrate + 0.5209 52.09%
CYP3A4 substrate + 0.5622 56.22%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.8403 84.03%
CYP3A4 inhibition - 0.5995 59.95%
CYP2C9 inhibition - 0.5280 52.80%
CYP2C19 inhibition + 0.5167 51.67%
CYP2D6 inhibition - 0.6616 66.16%
CYP1A2 inhibition + 0.8664 86.64%
CYP2C8 inhibition + 0.8133 81.33%
CYP inhibitory promiscuity + 0.7984 79.84%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7910 79.10%
Carcinogenicity (trinary) Non-required 0.6062 60.62%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9817 98.17%
Skin irritation - 0.8024 80.24%
Skin corrosion - 0.9430 94.30%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5541 55.41%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.8742 87.42%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.8412 84.12%
Acute Oral Toxicity (c) III 0.6395 63.95%
Estrogen receptor binding + 0.8314 83.14%
Androgen receptor binding + 0.8817 88.17%
Thyroid receptor binding + 0.5431 54.31%
Glucocorticoid receptor binding + 0.7733 77.33%
Aromatase binding + 0.7706 77.06%
PPAR gamma + 0.7094 70.94%
Honey bee toxicity - 0.8956 89.56%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.4917 49.17%

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 99.39% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.27% 98.95%
CHEMBL2535 P11166 Glucose transporter 93.93% 98.75%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 90.69% 92.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.44% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.20% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.58% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.01% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.43% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.23% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 84.29% 94.73%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 84.08% 81.14%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.81% 93.81%
CHEMBL4208 P20618 Proteasome component C5 83.51% 90.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 82.08% 83.10%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.00% 97.21%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 80.90% 96.67%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 80.86% 89.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.10% 99.17%

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.
There are no matching plants.

Cross-Links

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PubChem 179828
LOTUS LTS0097327
wikiData Q83024162