Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T73215 | Target Info | |||
Target Name | Leukocyte surface antigen Leu-16 (CD20) | ||||
Synonyms |
Membrane-spanning 4-domains subfamily A member 1; Leu-16; Bp35; B-lymphocyte surface antigen B1; B-lymphocyte antigen CD20
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Target Type | Successful Target | ||||
Gene Name | MS4A1 | ||||
Biochemical Class | CD20 calcium channel | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Angiotensinogenase renin (REN) | Successful Target | ||||
UniProt ID | RENI_HUMAN | |||||
Gene Name | REN | |||||
Synonyms |
Renin; Angiotensinogenase
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | Ki = 100 nM | [1] | ||
Co-Target Name | Cathepsin D (CTSD) | Clinical trial Target | ||||
UniProt ID | CATD_HUMAN | |||||
Gene Name | CTSD | |||||
Synonyms |
CPSD; CD
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 0.0016 ug.mL-1 | [2] | ||
Co-Target Name | Cathepsin L (CTSL) | Clinical trial Target | ||||
UniProt ID | CATL1_HUMAN | |||||
Gene Name | CTSL | |||||
Synonyms |
Major excreted protein; MEP; Cathepsin L1; CTSL1
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 800 nM | [3] | ||
Co-Target Name | Plasmodium Plasmepsin 2 (Malaria PLA2) | Patented-recorded Target | ||||
UniProt ID | PLM2_PLAFA | |||||
Gene Name | Malaria PLA2 | |||||
Synonyms |
Plasmepsin-2; PFAPD; Aspartic hemoglobinase II
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 0.42 nM | [4] | ||
Co-Target Name | Cathepsin E (CTSE) | Literature-reported Target | ||||
UniProt ID | CATE_HUMAN | |||||
Gene Name | CTSE | |||||
Synonyms |
Cathepsin E
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 0.08 nM | [5] | ||
Co-Target Name | Plasmodium Plasmepsin 1 (Malaria PLA1) | Literature-reported Target | ||||
UniProt ID | PLM1_PLAFA | |||||
Gene Name | Malaria PLA1 | |||||
Synonyms |
Plasmepsin I; PFAPG; Aspartic hemoglobinase I
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 0.9 nM | [4] | ||
Co-Target Name | Pepsinogen-5 (PGA5) | Literature-reported Target | ||||
UniProt ID | PEPA5_HUMAN | |||||
Gene Name | PGA5 | |||||
Synonyms |
Pepsin A-5
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 59 nM | [6] | ||
Co-Target Name | Disintegrin and metalloproteinase domain-containing protein 9 (ADAM9) | Co-Target | ||||
UniProt ID | ADAM9_HUMAN | |||||
Gene Name | ADAM9 | |||||
Synonyms |
ADAM 9; Cellular disintegrin-related protein; Meltrin-gamma; Metalloprotease/disintegrin/cysteine-rich protein 9; Myeloma cell metalloproteinase
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Representative Drug(s) | Iboctadekin + rituximab | Drug Info | IC50 = 56.3 nM | [7] |
References | Top | ||||
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REF 1 | Inhibition of the renin-angiotensin system. A new approach to the therapy of hypertension. J Med Chem. 1981 Apr;24(4):355-61. | ||||
REF 2 | Inhibition of Cathepsin D protease activity by. Med Chem Res. 2012 Dec 18;22:3953-8. | ||||
REF 3 | Identification of 3-acetyl-2-aminoquinolin-4-one as a novel, nonpeptidic scaffold for specific calpain inhibitory activity. J Med Chem. 2009 May 14;52(9):3093-7. | ||||
REF 4 | 2-Aminoquinazolin-4(3H)-one based plasmepsin inhibitors with improved hydrophilicity and selectivity. Bioorg Med Chem. 2018 May 15;26(9):2488-2500. | ||||
REF 5 | Tasiamide F, a potent inhibitor of cathepsins D and E from a marine cyanobacterium. Bioorg Med Chem. 2016 Aug 1;24(15):3276-82. | ||||
REF 6 | Auxiliary agents for the peroral administration of peptide and protein drugs: synthesis and evaluation of novel pepstatin analogues. J Med Chem. 1998 Jun 18;41(13):2339-44. | ||||
REF 7 | Grassystatins A-C from marine cyanobacteria, potent cathepsin E inhibitors that reduce antigen presentation. J Med Chem. 2009 Sep 24;52(18):5732-47. |
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