4-Chloro-D-threonine

Details

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Internal ID 022a2419-9bbc-49e0-a49c-6a9ceb521602
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name (2R,3R)-2-amino-4-chloro-3-hydroxybutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8ClNO3/c5-1-2(7)3(6)4(8)9/h2-3,7H,1,6H2,(H,8,9)/t2-,3+/m0/s1
InChI Key CETUIFTXYGHITB-STHAYSLISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8ClNO3
Molecular Weight 153.56 g/mol
Exact Mass 153.0192708 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -2.70
Atomic LogP (AlogP) -1.00
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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D-Threonine, 4-chloro-
132958-66-8
4-Chloro-D-threonine

2D Structure

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2D Structure of 4-Chloro-D-threonine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9119 91.19%
Caco-2 - 0.9595 95.95%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4793 47.93%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9696 96.96%
OATP1B3 inhibitior + 0.9131 91.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9528 95.28%
P-glycoprotein inhibitior - 0.9859 98.59%
P-glycoprotein substrate - 0.9857 98.57%
CYP3A4 substrate - 0.7409 74.09%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.7801 78.01%
CYP3A4 inhibition - 0.7935 79.35%
CYP2C9 inhibition - 0.9479 94.79%
CYP2C19 inhibition - 0.8601 86.01%
CYP2D6 inhibition - 0.8356 83.56%
CYP1A2 inhibition - 0.8643 86.43%
CYP2C8 inhibition - 0.9875 98.75%
CYP inhibitory promiscuity - 0.9782 97.82%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5872 58.72%
Eye corrosion - 0.9749 97.49%
Eye irritation - 0.5292 52.92%
Skin irritation - 0.7198 71.98%
Skin corrosion - 0.8148 81.48%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8168 81.68%
Micronuclear - 0.5526 55.26%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9350 93.50%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5551 55.51%
Estrogen receptor binding - 0.9100 91.00%
Androgen receptor binding - 0.9252 92.52%
Thyroid receptor binding - 0.7762 77.62%
Glucocorticoid receptor binding - 0.8639 86.39%
Aromatase binding - 0.8962 89.62%
PPAR gamma - 0.7020 70.20%
Honey bee toxicity - 0.9320 93.20%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.9052 90.52%
Fish aquatic toxicity - 0.9414 94.14%

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 99.04% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.51% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.83% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.27% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 81.07% 90.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.24% 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 71355953
LOTUS LTS0160625
wikiData Q104956045