MedKoo Cat#: 124506 | Name: Zosurabalpin

Description:

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

Zosurabalpin, also known as RG6006 and RO 7223280, is a small molecule, novel chemical class antibiotic for the treatment of Acinetobacter baumannii infections. Zosurabalpin disrupts the essential function of the LptB2FGC complex in Gram-negative bacteria and demonstrates efficacy against carbapenem-resistant Acinetobacter baumannii (CRAB). Zosurabalpin (RG6006) effectively treats highly drug-resistant contemporary isolates of CRAB both in vitro and in mouse models of infection, overcoming existing antibiotic resistance mechanisms.

Chemical Structure

Zosurabalpin
Zosurabalpin
CAS#2379336-76-0 (free base)

Theoretical Analysis

MedKoo Cat#: 124506

Name: Zosurabalpin

CAS#: 2379336-76-0 (free base)

Chemical Formula: C43H50N8O5S

Exact Mass: 790.3600

Molecular Weight: 790.98

Elemental Analysis: C, 65.29; H, 6.37; N, 14.17; O, 10.11; S, 4.05

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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Related CAS #
2379336-77-1 (TFA) 2379336-76-0 (free base)
Synonym
Zosurabalpin; RG 6006; RG-6006; RG6006; RO 7223280; RO-7223280; RO7223280;
IUPAC/Chemical Name
4-((7S,10S,13S)-13-((1H-indol-3-yl)methyl)-10-(4-aminobutyl)-7-(3-aminopropyl)-12-methyl-8,11,14-trioxo-5,6,7,8,9,10,11,12,13,14,15,16-dodecahydrobenzo[b]pyrido[3,2-p][1]thia[5,8,11,14]tetraazacycloheptadecin-17-yl)benzoic acid
InChi Key
NJFUXFYUHIHHOJ-FSEITFBQSA-N
InChi Code
InChI=1S/C43H50N8O5S/c1-51-37(23-30-25-47-34-12-3-2-10-32(30)34)40(53)49-26-33-31(27-16-18-28(19-17-27)43(55)56)11-6-15-38(33)57-41-29(9-8-22-46-41)24-48-35(14-7-21-45)39(52)50-36(42(51)54)13-4-5-20-44/h2-3,6,8-12,15-19,22,25,35-37,47-48H,4-5,7,13-14,20-21,23-24,26,44-45H2,1H3,(H,49,53)(H,50,52)(H,55,56)/t35-,36-,37-/m0/s1
SMILES Code
CN1[C@H](C(=O)NCC2=C(C=CC=C2SC3=C(CN[C@H](C(=O)N[C@H](C1=O)CCCCN)CCCN)C=CC=N3)C4=CC=C(C=C4)C(=O)O)CC5=CNC6=CC=CC=C65
Appearance
To be determined
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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
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
Carbapenem-resistant Acinetobacter baumannii (CRAB) has emerged as a major global pathogen with limited treatment options1. No new antibiotic chemical class with activity against A. baumannii has reached patients in over 50 years

Preparing Stock Solutions

The following data is based on the product molecular weight 790.98 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: Gibadullin R, Morris RK, Niu J, Sidney J, Sette A, Gellman SH. Thioamide Analogues of MHC I Antigen Peptides. J Am Chem Soc. 2023 Nov 29;145(47):25559-25569. doi: 10.1021/jacs.3c05300. Epub 2023 Nov 15. PMID: 37968794; PMCID: PMC10782604. 2: Lee HS, Wagner JL, Vugrin M, Brandenburg RT, Lee J, Miller L, Rayborn S, Hall RG. Insufficient Representation of Patients With Obesity in Randomized Controlled Trials Evaluating the Efficacy and Safety of Antimicrobials for Treatment of Skin and Skin Structure Infections: A Scoping Review. Open Forum Infect Dis. 2023 Mar 20;10(3):ofad144. doi: 10.1093/ofid/ofad144. PMID: 36998628; PMCID: PMC10043132. 3: Gu M, Jiang L, Hao L, Lu J, Liu Z, Lei Z, Li Y, Hua C, Li W, Li X. A novel theranostic nanoplatform for imaging-guided chemo-photothermal therapy in oral squamous cell carcinoma. J Mater Chem B. 2021 Aug 4;9(30):6006-6016. doi: 10.1039/d1tb01136g. PMID: 34282440. 4: Sartorius K, Swadling L, An P, Makarova J, Winkler C, Chuturgoon A, Kramvis A. The Multiple Roles of Hepatitis B Virus X Protein (HBx) Dysregulated MicroRNA in Hepatitis B Virus-Associated Hepatocellular Carcinoma (HBV-HCC) and Immune Pathways. Viruses. 2020 Jul 10;12(7):746. doi: 10.3390/v12070746. PMID: 32664401; PMCID: PMC7412373. 5: Lavin-Gonzalez P, Bourguignon C, Crescenzi O, Beaulieu S, Storch KF, Linnaranta O. Inactograms and objective sleep measures as means to capture subjective sleep problems in patients with a bipolar disorder. Bipolar Disord. 2020 Nov;22(7):722-730. doi: 10.1111/bdi.12903. Epub 2020 Apr 10. PMID: 32232937. 6: Salamah MF, Ravishankar D, Kodji X, Moraes LA, Williams HF, Vallance TM, Albadawi DA, Vaiyapuri R, Watson K, Gibbins JM, Brain SD, Perretti M, Vaiyapuri S. The endogenous antimicrobial cathelicidin LL37 induces platelet activation and augments thrombus formation. Blood Adv. 2018 Nov 13;2(21):2973-2985. doi: 10.1182/bloodadvances.2018021758. PMID: 30413433; PMCID: PMC6234361. 7: Caza JS, Atance CM. Children's behavior and spontaneous talk in a future thinking task. Psychol Res. 2019 Jun;83(4):761-773. doi: 10.1007/s00426-018-1089-1. Epub 2018 Sep 5. PMID: 30187115.