MedKoo Cat#: 565717 | Name: TBAJ-587 HCl

Description:

WARNING: This product is for research use only, not for human or veterinary use.

TBAJ-587 is a novel potent antituberculosis agent with minimal inhibition of the herg channel

Chemical Structure

TBAJ-587 HCl
TBAJ-587 HCl
CAS#TBAJ-587 HCl

Theoretical Analysis

MedKoo Cat#: 565717

Name: TBAJ-587 HCl

CAS#: TBAJ-587 HCl

Chemical Formula: C30H34BrClFN3O5

Exact Mass: 0.0000

Molecular Weight: 650.97

Elemental Analysis: C, 55.35; H, 5.26; Br, 12.27; Cl, 5.45; F, 2.92; N, 6.46; O, 12.29

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
TBAJ-587; TBAJ 587; TBAJ587
IUPAC/Chemical Name
(1S,2S)-1-(6-Bromo-2-methoxyquinolin-3-yl)-2-(2,6-dimethoxypyridin-4-yl)-4-(dimethylamino)-1-(2-fluoro-3-methoxyphenyl)butan-2-ol hydrochloride
InChi Key
GKQNVDCRTIBXEQ-KJVMAEBTSA-N
InChi Code
InChI=1S/C30H33BrFN3O5.ClH/c1-35(2)13-12-30(36,19-16-25(38-4)34-26(17-19)39-5)27(21-8-7-9-24(37-3)28(21)32)22-15-18-14-20(31)10-11-23(18)33-29(22)40-6;/h7-11,14-17,27,36H,12-13H2,1-6H3;1H/t27-,30-;/m1./s1
SMILES Code
O[C@](CCN(C)C)(C1=CC(OC)=NC(OC)=C1)[C@@H](C2=CC3=CC(Br)=CC=C3N=C2OC)C4=CC=CC(OC)=C4F.[H]Cl
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 650.97 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Fan J, Tan Z, He S, Li A, Jia Y, Li J, Zhang Z, Li B, Chu H. TBAJ-587, a novel diarylquinoline, is active against Mycobacterium abscessus. Antimicrob Agents Chemother. 2024 Oct 29:e0094524. doi: 10.1128/aac.00945-24. Epub ahead of print. PMID: 39470202. 2: Zhang Y, Lai Y, Zhou S, Ran T, Zhang Y, Zhao Z, Feng Z, Yu L, Xu J, Shi K, Wang J, Pang Y, Li L, Chen H, Guddat LW, Gao Y, Liu F, Rao Z, Gong H. Inhibition of M. tuberculosis and human ATP synthase by BDQ and TBAJ-587. Nature. 2024 Jul;631(8020):409-414. doi: 10.1038/s41586-024-07605-8. Epub 2024 Jul 3. PMID: 38961288. 3: Li S-Y, Tyagi S, Soni H, Betoudji F, Converse PJ, Mdluli K, Upton AM, Fotouhi N, Barros-Aguirre D, Ballell L, Jimenez-Navarro E, Nuermberger EL. Bactericidal and sterilizing activity of novel regimens combining bedaquiline or TBAJ-587 with GSK2556286 and TBA-7371 in a mouse model of tuberculosis. Antimicrob Agents Chemother. 2024 Apr 3;68(4):e0156223. doi: 10.1128/aac.01562-23. Epub 2024 Feb 20. PMID: 38376228; PMCID: PMC10989019. 4: Ahmad T, Gao F, Li J, Zhang Z, Song T, Yuan Q, Zhang W. Synergistic Li/Li Bimetallic System for the Asymmetric Synthesis of Antituberculosis Drug TBAJ-587. J Org Chem. 2023 Jun 2;88(11):7601-7606. doi: 10.1021/acs.joc.3c00705. Epub 2023 May 1. PMID: 37125776; PMCID: PMC10242759. 5: Li SY, Converse PJ, Betoudji F, Lee J, Mdluli K, Upton A, Fotouhi N, Nuermberger EL. Next-Generation Diarylquinolines Improve Sterilizing Activity of Regimens with Pretomanid and the Novel Oxazolidinone TBI-223 in a Mouse Tuberculosis Model. Antimicrob Agents Chemother. 2023 Apr 18;67(4):e0003523. doi: 10.1128/aac.00035-23. Epub 2023 Mar 15. PMID: 36920217; PMCID: PMC10112056. 6: Barbaro L, Nagalingam G, Triccas JA, Tan L, West NP, Priebbenow DL, Baell JB. Discovery of Anti-tubercular Analogues of Bedaquiline with Modified A-, B- and C-Ring Subunits. ChemMedChem. 2023 Jan 3;18(1):e202200533. doi: 10.1002/cmdc.202200533. Epub 2022 Nov 14. PMID: 36259365. 7: Black TA, Buchwald UK. The pipeline of new molecules and regimens against drug-resistant tuberculosis. J Clin Tuberc Other Mycobact Dis. 2021 Nov 5;25:100285. doi: 10.1016/j.jctube.2021.100285. PMID: 34816020; PMCID: PMC8593651. 8: Xu J, Converse PJ, Upton AM, Mdluli K, Fotouhi N, Nuermberger EL. Comparative Efficacy of the Novel Diarylquinoline TBAJ-587 and Bedaquiline against a Resistant Rv0678 Mutant in a Mouse Model of Tuberculosis. Antimicrob Agents Chemother. 2021 Mar 18;65(4):e02418-20. doi: 10.1128/AAC.02418-20. PMID: 33526488; PMCID: PMC8097419. 9: Sutherland HS, Tong AST, Choi PJ, Blaser A, Franzblau SG, Cooper CB, Upton AM, Lotlikar M, Denny WA, Palmer BD. Variations in the C-unit of bedaquiline provides analogues with improved biology and pharmacology. Bioorg Med Chem. 2020 Jan 1;28(1):115213. doi: 10.1016/j.bmc.2019.115213. Epub 2019 Nov 26. PMID: 31810890. 10: Kamariah N, Ragunathan P, Shin J, Saw WG, Wong CF, Dick T, Grüber G. Unique structural and mechanistic properties of mycobacterial F-ATP synthases: Implications for drug design. Prog Biophys Mol Biol. 2020 May;152:64-73. doi: 10.1016/j.pbiomolbio.2019.11.006. Epub 2019 Nov 16. PMID: 31743686.