Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T65291 | Target Info | |||
Target Name | Fatty aldehyde dehydrogenase (ALDH3A2) | ||||
Synonyms |
Microsomal aldehyde dehydrogenase; Aldehyde dehydrogenase family 3 member A2; Aldehyde dehydrogenase 10; ALDH10
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Target Type | Successful Target | ||||
Gene Name | ALDH3A2 | ||||
Biochemical Class | Aldehyde/oxo donor oxidoreductase | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Lysyl oxidase homolog 2 (LOXL2) | Clinical trial Target | ||||
UniProt ID | LOXL2_HUMAN | |||||
Gene Name | LOXL2 | |||||
Synonyms |
Lysyl oxidaserelated protein WS914; Lysyl oxidaserelated protein 2; Lysyl oxidaselike protein 2; LOXL2
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 150 nM | [1] | ||
Co-Target Name | Monoglyceride lipase (MAGL) | Clinical trial Target | ||||
UniProt ID | MGLL_HUMAN | |||||
Gene Name | MGLL | |||||
Synonyms |
Monoacylglycerol lipase; MGL; Lysophospholipaselike; Lysophospholipase-like; Lysophospholipase homolog; HUK5; HU-K5
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 360 nM | [2] | ||
Co-Target Name | Lysyl oxidase (LOX) | Literature-reported Target | ||||
UniProt ID | LYOX_HUMAN | |||||
Gene Name | LOX | |||||
Synonyms |
Protein-lysine 6-oxidase
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 320 nM | [1] | ||
Co-Target Name | Histone-lysine N-methyltransferase EHMT2 (EHMT2) | Literature-reported Target | ||||
UniProt ID | EHMT2_HUMAN | |||||
Gene Name | EHMT2 | |||||
Synonyms |
Protein G9a; NG36; Lysine N-methyltransferase 1C; KMT1C; Histone H3-K9 methyltransferase 3; HLA-B-associated transcript 8; H3-K9-HMTase 3; G9A; Euchromatic histone-lysine N-methyltransferase 2; C6orf30; BAT8
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 600 nM | [3] | ||
Co-Target Name | Lysyl oxidase homolog 4 (LOXL4) | Co-Target | ||||
UniProt ID | LOXL4_HUMAN | |||||
Gene Name | LOXL4 | |||||
Synonyms |
Lysyl oxidase-like protein 4; Lysyl oxidase-related protein C
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 59 nM | [1] | ||
Co-Target Name | Lysyl oxidase homolog 3 (LOXL3) | Co-Target | ||||
UniProt ID | LOXL3_HUMAN | |||||
Gene Name | LOXL3 | |||||
Synonyms |
Lysyl oxidase-like protein 3
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 93 nM | [1] | ||
Co-Target Name | Gasdermin-D (GSDMD) | Co-Target | ||||
UniProt ID | GSDMD_HUMAN | |||||
Gene Name | GSDMD | |||||
Synonyms |
Gasdermin domain-containing protein 1
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Representative Drug(s) | Disulfiram | Drug Info | IC50 = 400 nM | [4] |
References | Top | ||||
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REF 1 | Inhibition of the LOX enzyme family members with old and new ligands. Selectivity analysis revisited. Bioorg Med Chem Lett. 2018 Oct 1;28(18):3113-3118. | ||||
REF 2 | Therapeutic Potential of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and N-Acylethanolamine Acid Amidase Inhibitors. J Med Chem. 2017 Jan 12;60(1):4-46. | ||||
REF 3 | Inhibition of histone lysine methyltransferases G9a and GLP by ejection of structural Zn(II). Bioorg Med Chem Lett. 2018 Apr 15;28(7):1234-1238. | ||||
REF 4 | Gasdermin D (GSDMD) as a new target for the treatment of infection. Med. Chem. Commun. 2019;10:660-667. |
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