Ac-r-N-DMAT

Details

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Internal ID be5fc40d-fe20-4300-a5db-331d75247eaa
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids
IUPAC Name 2-acetamido-3-[1-(2-methylbut-3-en-2-yl)indol-3-yl]propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H22N2O3/c1-5-18(3,4)20-11-13(14-8-6-7-9-16(14)20)10-15(17(22)23)19-12(2)21/h5-9,11,15H,1,10H2,2-4H3,(H,19,21)(H,22,23)
InChI Key LLVOASVXELWNBZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22N2O3
Molecular Weight 314.40 g/mol
Exact Mass 314.16304257 g/mol
Topological Polar Surface Area (TPSA) 71.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 3
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 Ac-r-N-DMAT

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9248 92.48%
Caco-2 - 0.5599 55.99%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5630 56.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9032 90.32%
OATP1B3 inhibitior + 0.9351 93.51%
MATE1 inhibitior - 0.9231 92.31%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5881 58.81%
P-glycoprotein inhibitior - 0.8482 84.82%
P-glycoprotein substrate - 0.6711 67.11%
CYP3A4 substrate + 0.5741 57.41%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.8585 85.85%
CYP3A4 inhibition - 0.5585 55.85%
CYP2C9 inhibition - 0.7460 74.60%
CYP2C19 inhibition - 0.5971 59.71%
CYP2D6 inhibition - 0.8948 89.48%
CYP1A2 inhibition - 0.7718 77.18%
CYP2C8 inhibition - 0.7934 79.34%
CYP inhibitory promiscuity - 0.7042 70.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5959 59.59%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9872 98.72%
Skin irritation - 0.7948 79.48%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6860 68.60%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5951 59.51%
skin sensitisation - 0.8535 85.35%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.4602 46.02%
Acute Oral Toxicity (c) III 0.5190 51.90%
Estrogen receptor binding - 0.5151 51.51%
Androgen receptor binding - 0.5279 52.79%
Thyroid receptor binding - 0.5366 53.66%
Glucocorticoid receptor binding + 0.6236 62.36%
Aromatase binding + 0.5854 58.54%
PPAR gamma + 0.5246 52.46%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9562 95.62%

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 98.29% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.49% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.14% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.43% 91.11%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 90.07% 94.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.78% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.39% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.72% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.80% 93.56%
CHEMBL5028 O14672 ADAM10 84.67% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.66% 96.00%
CHEMBL230 P35354 Cyclooxygenase-2 83.83% 89.63%
CHEMBL1255126 O15151 Protein Mdm4 82.82% 90.20%
CHEMBL3401 O75469 Pregnane X receptor 81.80% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 81.42% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.79% 99.23%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.78% 98.33%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 80.34% 81.29%

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 139591560
LOTUS LTS0118255
wikiData Q104171078