PM-94128

Details

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Internal ID d0e85b43-0be4-434b-94ed-c7c35676ef98
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Amino acids and derivatives > Gamma amino acids and derivatives
IUPAC Name 4-amino-2,3-dihydroxy-N-[1-(8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl)-3-methylbutyl]-6-methylheptanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H34N2O6/c1-11(2)8-14(23)19(26)20(27)21(28)24-15(9-12(3)4)17-10-13-6-5-7-16(25)18(13)22(29)30-17/h5-7,11-12,14-15,17,19-20,25-27H,8-10,23H2,1-4H3,(H,24,28)
InChI Key ZGMSHKBULLTJHQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34N2O6
Molecular Weight 422.50 g/mol
Exact Mass 422.24168681 g/mol
Topological Polar Surface Area (TPSA) 142.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of PM-94128

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6632 66.32%
Caco-2 - 0.7116 71.16%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4190 41.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9090 90.90%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 0.9046 90.46%
OCT2 inhibitior - 0.9817 98.17%
BSEP inhibitior - 0.8797 87.97%
P-glycoprotein inhibitior - 0.6491 64.91%
P-glycoprotein substrate + 0.7479 74.79%
CYP3A4 substrate + 0.5996 59.96%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.7913 79.13%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.8884 88.84%
CYP2C19 inhibition - 0.8397 83.97%
CYP2D6 inhibition - 0.8836 88.36%
CYP1A2 inhibition - 0.8166 81.66%
CYP2C8 inhibition - 0.8445 84.45%
CYP inhibitory promiscuity - 0.9340 93.40%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5037 50.37%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9736 97.36%
Skin irritation - 0.8168 81.68%
Skin corrosion - 0.9446 94.46%
Ames mutagenesis - 0.5254 52.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5440 54.40%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5818 58.18%
skin sensitisation - 0.8791 87.91%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.4542 45.42%
Acute Oral Toxicity (c) III 0.5936 59.36%
Estrogen receptor binding + 0.6938 69.38%
Androgen receptor binding + 0.6111 61.11%
Thyroid receptor binding + 0.5825 58.25%
Glucocorticoid receptor binding - 0.5323 53.23%
Aromatase binding - 0.5298 52.98%
PPAR gamma + 0.5784 57.84%
Honey bee toxicity - 0.9251 92.51%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.7110 71.10%

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
CHEMBL2581 P07339 Cathepsin D 98.49% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.73% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.92% 95.56%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 95.41% 83.10%
CHEMBL3359 P21462 Formyl peptide receptor 1 93.04% 93.56%
CHEMBL2094135 Q96BI3 Gamma-secretase 92.91% 98.05%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.99% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.34% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.24% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.09% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 87.00% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.66% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.68% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 84.09% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.62% 95.89%
CHEMBL236 P41143 Delta opioid receptor 83.18% 99.35%
CHEMBL5028 O14672 ADAM10 82.48% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.42% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 82.04% 93.31%
CHEMBL221 P23219 Cyclooxygenase-1 81.61% 90.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 9888503
LOTUS LTS0261089
wikiData Q105375327