BMS-626529 [701213-36-7]
Referentie A3253-10mg
Formaat : 10mg
Merk : APExBIO Technology
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BMS-626529
mRNA synthesis
In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
Tyramide Signal Amplification (TSA)
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
Phos Binding Reagent Acrylamide
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
Cell Counting Kit-8 (CCK-8)
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
Inhibitor Cocktails
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
EC50
HIV-1 attachment inhibitors represent a new class of entry inhibitors that prevent the initial interaction between virus and host cell by binding to the viral envelope protein gp120 and blocking attachment of the virus to the CD4 receptor on CD4+ T-cells. BMS-626529 is a novel small-molecule attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T-cells.
In vitro: The activity of BMS-626529 is virus dependent, due to heterogeneity within gp120. BMS-626529 had half-maximal effective concentration values of6 log10, with half-maximal effective concentration values in the low pM range against the most susceptible viruses. Measurement of the binding affinity of BMS-626529 for purified gp120 suggests that a contributory factor to its inhibitory potency may be a relatively long dissociative half-life [1].
In vivo: No animal in-vivo data available currently
Clinical trial: BMS-663068 is a prodrug of the small-molecule inhibitor BMS-626529. The maximum median decreased in plasma HIV-1 RNA load from baseline ranged from 1.21 to 1.73 log10 copies/mL. Plasma concentrations of BMS-626529 were not associated with an antiviral response, while low baseline inhibitory concentrations and the minimum and average steady-state BMS-626529 plasma concentrations, when adjusted by the baseline protein binding–adjusted 90% inhibitory concentration, were linked with antiviral response. BMS-663068 was generally well tolerated [2].
References:
[1] Nowicka-Sans B, Gong YF, McAuliffe B, Dicker I, Ho HT, Zhou N, Eggers B, Lin PF, Ray N, Wind-Rotolo M, Zhu L, Majumdar A, Stock D, Lataillade M, Hanna GJ, Matiskella JD, Ueda Y, Wang T, Kadow JF, Meanwell NA, Krystal M. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob Agents Chemother. 2012;56(7):3498-507.
[2] Nettles RE, Schürmann D, Zhu L, Stonier M, Huang SP, Chang I, Chien C, Krystal M, Wind-Rotolo M, Ray N, Hanna GJ, Bertz R, Grasela D. Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects. J Infect Dis. 2012;206(7):1002-11.
- 1. Marianne Boutin, Halima Medjahed, et al. "Temsavir Modulates HIV-1 Envelope Conformation by Decreasing Its Proteolytic Cleavage." Viruses. 2023 May 18;15(5):1189. PMID: 37243275
- 2. Jonathan Richard, Jérémie Prévost, et al. "Temsavir blocks the immunomodulatory activities of HIV-1 soluble gp120." Cell Chem Biol. 2023 May 18;30(5):540-552.e6. PMID: 36958337
- 3. Boutin, Marianne. "Impact du petit inhibiteur temsavir sur la conformation des glycoprotéines d’enveloppe du VIH-1." Université de Montréal. 2023-05.
- 4. Cheryl A. Stoddart, Francesca Curreli, et al. "Comparative Pharmacokinetics of a Dual Inhibitor of HIV-1, NBD-14189, in Rats and Dogs with a Proof-of-Concept Evaluation of Antiviral Potency in SCID-hu Mouse Model." Viruses 2022. PMID: 35922005
- 5. Jérémie Prévost, Halima Medjahed, et al. "HIV-1 envelope glycoproteins proteolytic cleavage protects infected cells from ADCC mediated by plasma from infected individuals." Viruses. 2021 Nov 6;13(11):2236. PMID: 34835042
- 6. Lu M, Ma X, et al. "Shedding-resistant HIV-1 envelope glycoproteins adopt downstream conformations that remain responsive to conformation-preferring ligands." J Virol. 2020;JVI.00597-20. PMID: 32522853
- 7. Stadtmueller BM, Bridges MD, et al. "DEER Spectroscopy Measurements Reveal Multiple Conformations of HIV-1 SOSIP Envelopes that Show Similarities with Envelopes on Native Virions."Immunity. 2018 Aug 21;49(2):235-246.e4. PMID: 30076100
- 8. Pancera M, Lai YT, et al. "Crystal structures of trimeric HIV envelope with entry inhibitors BMS-378806 and BMS-626529." Nat Chem Biol. 2017 Oct;13(10):1115-1122. PMID: 28825711
| Physical Appearance | A solid |
| Storage | Store at -20°C |
| M.Wt | 473.48 |
| Cas No. | 701213-36-7 |
| Formula | C24H23N7O4 |
| Synonyms | BMS 626529;BMS626529 |
| Solubility | insoluble in H2O; insoluble in EtOH; ≥1.48 mg/mL in DMSO |
| Chemical Name | 1-(4-benzoylpiperazin-1-yl)-2-[4-methoxy-7-(3-methyl-1,2,4-triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]ethane-1,2-dione |
| SDF | Download SDF |
| Canonical SMILES | CC1=NN(C=N1)C2=NC=C(C3=C2NC=C3C(=O)C(=O)N4CCN(CC4)C(=O)C5=CC=CC=C5)OC |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |
| Kinase experiment [1]: | |
| Binding assays | MicroBioSpin 6 columns were used to measure the binding of [3H]BMS-626529 to gp120. Binding solutions (30 μl) containing 25 mM Tris-HCl (pH 7.5), 125 mM NaCl, 50 nM gp120JRFL, and serial dilutions of [3H]BMS-626529 were allowed to equilibrate and then adsorbed to a MicroBioSpin 6 column. The column was centrifuged (14,000 rpm) for 5 min, the eluent was collected, and radioactivity was determined with a scintillation counter. To measure dissociative kinetics, 150 nM [3H]BMS-626529 was incubated with 60 nM gp120 at ambient temperature for 1 h to achieve equilibrium binding, and then a large molar excess (14-fold) of soluble CD4 protein was added to drive dissociation. Aliquots were taken at the indicated time intervals, adsorbed to a spin column, and centrifuged, and the radioactivity in the eluent was quantitated. Comparison of the tritium signal from parallel samples with and without the soluble CD4 challenge allowed for the determination of the percent compound bound. |
| Cell experiment [1]: | |
| Cell lines | PBMCs infected with HIV-1 clinical isolates; MT-2 and PM1 cells |
| Preparation method | Soluble in DMSO. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months. |
| Reaction Conditions | 6 days; dissolved in 100% dimethyl sulfoxide (DMSO) and serially diluted to the desired concentration such that the final DMSO concentration in cell culture assays was 1%. |
| Applications | BMS-626529 exhibits low cytotoxicity in several cell types from different human tissues such as MT-2 (T lymphocytes), HEK293 (kidney), PM1 and PBMCs. BMS-626529 exhibits EC50 value against the CXCR4-tropic LAI virus of 0.7 nM and also exhibits broad spectrum of activity. |
| Human experiment [2]: | |
| Patients | Adults (aged ≥18 years) infected with subtype B HIV-1. |
| Dosage form | 600 mg or 1200mg with or without 100 mg ritonavir; 8 days; orally administrated. |
| Applications | BMS-663068, the prodrug of BMS-626529, reduces plasma HIV-1 RNA levels and increases median absolute CD4+ T-cell counts. Also, BMS-663068 is well tolerated. BMS-626529 has favorable pharmacokinetics following administration of the prodrug BMS-663068. |
| Other notes | Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
| References: [1]. Nowicka-Sans B, Gong YF, McAuliffe B, et al. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob Agents Chemother, 2012, 56(7): 3498-3507. [2]. Nettles RE, Schürmann D, Zhu L, et al. Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects. J Infect Dis, 2012, 206(7): 1002-1011. | |
| Description | BMS-626529 is a small-molecule attachment inhibitor of HIV-1 gp120 with IC50 values of 2.26 nM, 0.34 nM and 1.3 nM for HIV-1 subtype A, B, and C envelope, respectively. | |||||
| Targets | HIV-1 subtype A envelope | HIV-1 subtype B envelope | HIV-1 subtype C envelope | |||
| IC50 | 2.26 nM | 0.34 nM | 1.3 nM | |||