Target Poor or Non Binder(s) Information
Target General Information | Top | ||||
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Target ID | T36806 | Target Info | |||
Target Name | Kidney-type arginase (ARG2) | ||||
Synonyms |
Non-hepatic arginase; Human penile arginase; Arginase II; ARG2
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Target Type | Clinical trial Target | ||||
Gene Name | ARG2 | ||||
Biochemical Class | Carbon-nitrogen hydrolase | ||||
UniProt ID |
Poor Binders of This Target (in total, 1 binders) | Download | Top | |||
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Compound Name |
2-Amino-6-borono-2-(2-hydroxyethyl)hexanoic acid
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Investigative | Compound Info | ||
Synonyms |
CHEMBL2348494; BDBM50431957
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Activity |
IC50 = 57000 nM
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[1] |
Non Binders of This Target (in total, 3 non binders) | Download | Top | |||
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Compound Name |
(2S)-2-Amino-6-borono-2-(2-piperidin-1-ylethyl)hexanoic acid
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Investigative | Compound Info | ||
Synonyms |
CHEMBL2326091; SCHEMBL10207709; BDBM50427902; ZINC170183245
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Activity |
IC50 > 300000 nM
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[2] | |||
Compound Name |
Chembl4250607
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Investigative | Compound Info | ||
Synonyms |
BDBM50462601
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Activity |
Ki = 322000 nM
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[3] | |||
Compound Name |
Chembl4238387
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Investigative | Compound Info | ||
Synonyms |
BDBM50462600
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Activity |
Ki = 437000 nM
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[3] |
References | Top | ||||
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REF 1 | 2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors. Bioorg Med Chem Lett. 2013 Apr 1;23(7):2027-30. | ||||
REF 2 | Discovery of (R)-2-amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic acid and congeners as highly potent inhibitors of human arginases I and II for treatment of myocardial reperfusion injury. J Med Chem. 2013 Mar 28;56(6):2568-80. | ||||
REF 3 | Rational design of novel irreversible inhibitors for human arginase. Bioorg Med Chem. 2018 Aug 7;26(14):3939-3946. |
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