SB-756050
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MedKoo CAT#: 528518

CAS#: 447410-57-3

Description: SB-756050 is a G protein-coupled bile acid receptor 1 (GPBAR1) agonist potentially for the treatment of type 2 diabetes.


Chemical Structure

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SB-756050
CAS# 447410-57-3

Theoretical Analysis

MedKoo Cat#: 528518
Name: SB-756050
CAS#: 447410-57-3
Chemical Formula: C21H28N2O8S2
Exact Mass: 500.13
Molecular Weight: 500.580
Elemental Analysis: C, 50.39; H, 5.64; N, 5.60; O, 25.57; S, 12.81

Price and Availability

Size Price Availability Quantity
100mg USD 350
250mg USD 750
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Synonym: SB-756050; SB 756050; SB756050

IUPAC/Chemical Name: 1,4-bis((3,4-dimethoxyphenyl)sulfonyl)-1,4-diazepane

InChi Key: GJUFPAZNBPFNRI-UHFFFAOYSA-N

InChi Code: InChI=1S/C21H28N2O8S2/c1-28-18-8-6-16(14-20(18)30-3)32(24,25)22-10-5-11-23(13-12-22)33(26,27)17-7-9-19(29-2)21(15-17)31-4/h6-9,14-15H,5,10-13H2,1-4H3

SMILES Code: O=S(N1CCN(S(=O)(C2=CC=C(OC)C(OC)=C2)=O)CCC1)(C3=CC=C(OC)C(OC)=C3)=O

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: >2 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:

Product Data:
Biological target: SB-756050 is an agonist of TGR5 (EC50 = 1.3 μM for the human receptor). It is selective for TGR5 over the farnesoid X receptor (FXR) and a panel of other receptors, channels, and transporters.
In vitro activity: To be determined
In vivo activity: In a type 2 diabetes clinical trial, SB-756050 was well-tolerated. It was readily absorbed, exhibited nonlinear pharmacokinetics with a less than dose-proportional increase in plasma exposure above 100 mg, and demonstrated no significant changes in exposure when co-administered with sitagliptin. The glucose effects of SB-756050 + sitagliptin were comparable to those of sitagliptin alone,despite differences in gut hormone plasma profiles. Reference: Clin Pharmacol Drug Dev. 2013 Jul;2(3):213-22. https://pubmed.ncbi.nlm.nih.gov/27121782/

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMF 10.0 19.98
DMSO 10.0 19.98

Preparing Stock Solutions

The following data is based on the product molecular weight 500.58 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
Formulation protocol: 1. Hodge RJ, Lin J, Vasist Johnson LS, Gould EP, Bowers GD, Nunez DJ; SB-756050 Project Team. Safety, Pharmacokinetics, and Pharmacodynamic Effects of a Selective TGR5 Agonist, SB-756050, in Type 2 Diabetes. Clin Pharmacol Drug Dev. 2013 Jul;2(3):213-22. doi: 10.1002/cpdd.34. Epub 2013 May 14. PMID: 27121782.
In vitro protocol: To be determined
In vivo protocol: 1. Hodge RJ, Lin J, Vasist Johnson LS, Gould EP, Bowers GD, Nunez DJ; SB-756050 Project Team. Safety, Pharmacokinetics, and Pharmacodynamic Effects of a Selective TGR5 Agonist, SB-756050, in Type 2 Diabetes. Clin Pharmacol Drug Dev. 2013 Jul;2(3):213-22. doi: 10.1002/cpdd.34. Epub 2013 May 14. PMID: 27121782.

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1: Hodge RJ, Lin J, Vasist Johnson LS, Gould EP, Bowers GD, Nunez DJ; SB-756050 Project Team.. Safety, Pharmacokinetics, and Pharmacodynamic Effects of a Selective TGR5 Agonist, SB-756050, in Type 2 Diabetes. Clin Pharmacol Drug Dev. 2013 Jul;2(3):213-22. doi: 10.1002/cpdd.34. Epub 2013 May 14. PubMed PMID: 27121782.