Atransfusarin

Details

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Internal ID 18d745d0-3b3d-4b02-8b03-cc9ef8cc1e3c
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids and derivatives
IUPAC Name methyl 2-[[5-[(3S)-3-hydroxybutyl]pyridine-2-carbonyl]amino]acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18N2O4/c1-9(16)3-4-10-5-6-11(14-7-10)13(18)15-8-12(17)19-2/h5-7,9,16H,3-4,8H2,1-2H3,(H,15,18)/t9-/m0/s1
InChI Key AFHZRVUWHGTZOB-VIFPVBQESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18N2O4
Molecular Weight 266.29 g/mol
Exact Mass 266.12665706 g/mol
Topological Polar Surface Area (TPSA) 88.50 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Atransfusarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8408 84.08%
Caco-2 + 0.5353 53.53%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7966 79.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8540 85.40%
P-glycoprotein inhibitior - 0.9518 95.18%
P-glycoprotein substrate - 0.5350 53.50%
CYP3A4 substrate + 0.5451 54.51%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.8329 83.29%
CYP2C9 inhibition - 0.8468 84.68%
CYP2C19 inhibition - 0.8639 86.39%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.8509 85.09%
CYP2C8 inhibition - 0.8289 82.89%
CYP inhibitory promiscuity - 0.9659 96.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6979 69.79%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.9720 97.20%
Skin irritation - 0.8145 81.45%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5988 59.88%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9214 92.14%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8043 80.43%
Acute Oral Toxicity (c) III 0.6873 68.73%
Estrogen receptor binding - 0.7322 73.22%
Androgen receptor binding - 0.8522 85.22%
Thyroid receptor binding + 0.6139 61.39%
Glucocorticoid receptor binding + 0.7179 71.79%
Aromatase binding - 0.7147 71.47%
PPAR gamma - 0.6564 65.64%
Honey bee toxicity - 0.7936 79.36%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.9366 93.66%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.52% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 94.02% 89.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.28% 94.45%
CHEMBL3437 Q16853 Amine oxidase, copper containing 92.25% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 91.70% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.95% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.76% 99.17%
CHEMBL2535 P11166 Glucose transporter 89.06% 98.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.81% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.48% 94.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.48% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.13% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.13% 90.71%
CHEMBL4208 P20618 Proteasome component C5 84.08% 90.00%
CHEMBL4040 P28482 MAP kinase ERK2 83.59% 83.82%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.15% 95.50%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 82.57% 95.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.18% 96.00%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 81.94% 89.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.93% 95.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.79% 92.29%

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 146683511
LOTUS LTS0271217
wikiData Q104911243