Oximoaspergillimide

Details

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Internal ID 4bafec09-f58f-4e93-b529-2fd4f4a019fd
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Oximes > Ketoximes
IUPAC Name (2Z)-2-hydroxyimino-4-methyl-N-(3-methylbutanoyl)pentanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20N2O3/c1-7(2)5-9(13-16)11(15)12-10(14)6-8(3)4/h7-8,16H,5-6H2,1-4H3,(H,12,14,15)/b13-9-
InChI Key ZBPZAHHJROEFGA-LCYFTJDESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20N2O3
Molecular Weight 228.29 g/mol
Exact Mass 228.14739250 g/mol
Topological Polar Surface Area (TPSA) 78.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.55
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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(2Z)-2-hydroxyimino-4-methyl-N-(3-methylbutanoyl)pentanamide
RefChem:168929
(2E)-2-hydroxyimino-4-methyl-N-(3-methylbutanoyl)pentanamide
CHEBI:202771

2D Structure

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2D Structure of Oximoaspergillimide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8329 83.29%
Caco-2 + 0.5840 58.40%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7459 74.59%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9457 94.57%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9253 92.53%
P-glycoprotein inhibitior - 0.9528 95.28%
P-glycoprotein substrate - 0.9040 90.40%
CYP3A4 substrate - 0.6191 61.91%
CYP2C9 substrate + 0.6063 60.63%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9194 91.94%
CYP2C9 inhibition - 0.9078 90.78%
CYP2C19 inhibition - 0.8599 85.99%
CYP2D6 inhibition - 0.9179 91.79%
CYP1A2 inhibition - 0.8579 85.79%
CYP2C8 inhibition - 0.9893 98.93%
CYP inhibitory promiscuity - 0.9776 97.76%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5520 55.20%
Eye corrosion - 0.9585 95.85%
Eye irritation + 0.5927 59.27%
Skin irritation - 0.7483 74.83%
Skin corrosion - 0.9284 92.84%
Ames mutagenesis - 0.6036 60.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5773 57.73%
Micronuclear + 0.7800 78.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8504 85.04%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5772 57.72%
Acute Oral Toxicity (c) III 0.6078 60.78%
Estrogen receptor binding - 0.7060 70.60%
Androgen receptor binding - 0.7898 78.98%
Thyroid receptor binding + 0.5417 54.17%
Glucocorticoid receptor binding - 0.6995 69.95%
Aromatase binding - 0.6386 63.86%
PPAR gamma - 0.7968 79.68%
Honey bee toxicity - 0.9560 95.60%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.8054 80.54%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.24% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.81% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.78% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.13% 96.47%
CHEMBL2885 P07451 Carbonic anhydrase III 86.30% 87.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.93% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.78% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 82.72% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.90% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.92% 96.95%

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 132604365
LOTUS LTS0029096
wikiData Q77373430