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BOC Sciences |
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| | PD 135390 Basic information |
| Product Name: | PD 135390 | | Synonyms: | PD 135390;Glycinamide, N-(4-morpholinylsulfonyl)phenylalanyl-N-[4-[(butylamino)carbonyl]-1-(cyclohexylmethyl)-2-hydroxy-5-methylhexyl]-2-(2-propenylthio)- (9CI);(Rac)-PD 135390 | | CAS: | 150351-31-8 | | MF: | C37H61N5O7S2 | | MW: | 752.04 | | EINECS: | | | Product Categories: | | | Mol File: | 150351-31-8.mol |  |
| | PD 135390 Chemical Properties |
| density | 1.21±0.1 g/cm3(Predicted) | | pka | 10.88±0.20(Predicted) |
| | PD 135390 Usage And Synthesis |
| Description | PD 135390 is a novel HIV-1 protease inhibitors identified by rational selection. The human immunodeficiency virus (HIV-1), associated with the AIDS (acquired immunodeficiency syndrome) epidemic, encodes an aspartyl protease that is essential for polyprotein processing in the virus (Navia et al., 1989). It has been demonstrated that inactivation of the protease either catalytically or by an inhibitor prevents infectious virion formation (Kohl et al., 1988; Darke et al., 1989). The acquired knowledge of key molecular interactions occurring between inhibitors and aspartyl proteases, as well as the structural similarities between HIV-1 protease and human renin was used to rationally select candidates for HIV-1 screening from the pool of analogs designed as renin inhibitors. A minimal number of chosen compounds were tested in an HIV-1 protease assay system. Two structurally novel peptides emerged as potent enzymatic protease inhibitors. This study highlights the selection process and characterizes the antiviral properties of the two novel analogs. | | Uses | (Rac)-PD 135390 is a dipeptide and an HIV-1 protease inhibitor with an IC50 of 2 nM. (Rac)-PD 135390 can be utilized in antiviral research[1]. | | References | [1] Humblet CC, et al. Characterization of two structurally novel HIV-1 protease inhibitors identified by rational selection. Antiviral Res. 1993 May;21(1):73-84. DOI:10.1016/0166-3542(93)90068-t |
| | PD 135390 Preparation Products And Raw materials |
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