SRI-37330 HCl
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MedKoo CAT#: 463768

CAS#: 2322245-49-6 (HCl)

Description: SRI-37330 hydrochloride is a novel inhibitor of TXNIP expression, decreasing glucagon secretion and action and blocking hepatic glucose output, reversing obesity- and STZ-induced diabetes and hepatic steatosis.


Chemical Structure

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SRI-37330 HCl
CAS# 2322245-49-6 (HCl)

Theoretical Analysis

MedKoo Cat#: 463768
Name: SRI-37330 HCl
CAS#: 2322245-49-6 (HCl)
Chemical Formula: C16H20ClF3N4O2S
Exact Mass: 0.00
Molecular Weight: 424.867
Elemental Analysis: C, 45.23; H, 4.75; Cl, 8.34; F, 13.41; N, 13.19; O, 7.53; S, 7.55

Price and Availability

Size Price Availability Quantity
1mg USD 80 Ready to ship
5mg USD 150 Ready to ship
10mg USD 250 Ready to ship
25mg USD 550 Ready to ship
50mg USD 950 Ready to ship
100mg USD 1650 Ready to ship
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Related CAS #: 2322245-49-6 (HCl)   2322245-42-9 (free base)    

Synonym: SRI-37330 hydrochloride; SRI37330 hydrochloride; SRI 37330 hydrochloride; SRI-37330 HCl; SRI37330 HCl; SRI 37330 HCl;

IUPAC/Chemical Name: N-((1-(6-(trifluoromethyl)quinazolin-4-yl)piperidin-3-yl)methyl)methanesulfonamide hydrochloride

InChi Key: SIWGSSRKYJTJTF-UHFFFAOYSA-N

InChi Code: InChI=1S/C16H19F3N4O2S.ClH/c1-26(24,25)22-8-11-3-2-6-23(9-11)15-13-7-12(16(17,18)19)4-5-14(13)20-10-21-15;/h4-5,7,10-11,22H,2-3,6,8-9H2,1H3;1H

SMILES Code: CS(=O)(NCC1CN(C2=C3C=C(C(F)(F)F)C=CC3=NC=N2)CCC1)=O.[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: >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:

Biological target: SRI-37330 hydrochloride is an orally bioavailable thioredoxin-interacting protein (TXNIP) inhibitor.
In vitro activity: Transient transfection experiments showed that SRI-37330 inhibited the activity of the human TXNIP promoter in INS-1 cells by ~70% (Fig. 1b), consistent with inhibition at the transcriptional level. SRI-37330 also inhibited endogenous TXNIP mRNA expression as shown by 7-point dose-response qRT-PCR assays (Fig. 1c), revealing an IC50 of 0.64 μM and no cytotoxicity (Supplemental Table S1a). Similarly, SRI-37330 also inhibited TXNIP protein levels in a dose-dependent manner (Fig. 1d). Reference: Cell Metab. 2020 Sep 1;32(3):353-365.e8. https://pubmed.ncbi.nlm.nih.gov/32726606/
In vivo activity: Intraperitoneal glucose tolerance tests (GTTs) revealed a consistently and significantly improved glucose tolerance in response to SRI37330 administration (Fig. 3c), whereas insulin tolerance tests (ITTs) remained unaltered (Fig. 3d). Fasting blood glucose was slightly, but significantly lower in SRI-37330-treated mice (Fig. 3e). Notably, while fasting serum insulin levels were unchanged in SRI-37330-treated mice as compared to controls (Fig. 3f), fasting serum glucagon levels were lower (Fig. 3g), suggesting that SRI37330 may also affect glucagon secretion from pancreatic alpha cells. Reference: Cell Metab. 2020 Sep 1;32(3):353-365.e8. https://pubmed.ncbi.nlm.nih.gov/32726606/

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 62.5 147.10

Preparing Stock Solutions

The following data is based on the product molecular weight 424.87 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. Thielen LA, Chen J, Jing G, Moukha-Chafiq O, Xu G, Jo S, Grayson TB, Lu B, Li P, Augelli-Szafran CE, Suto MJ, Kanke M, Sethupathy P, Kim JK, Shalev A. Identification of an Anti-diabetic, Orally Available Small Molecule that Regulates TXNIP Expression and Glucagon Action. Cell Metab. 2020 Sep 1;32(3):353-365.e8. doi: 10.1016/j.cmet.2020.07.002. Epub 2020 Jul 28. PMID: 32726606; PMCID: PMC7501995.
In vitro protocol: 1. Thielen LA, Chen J, Jing G, Moukha-Chafiq O, Xu G, Jo S, Grayson TB, Lu B, Li P, Augelli-Szafran CE, Suto MJ, Kanke M, Sethupathy P, Kim JK, Shalev A. Identification of an Anti-diabetic, Orally Available Small Molecule that Regulates TXNIP Expression and Glucagon Action. Cell Metab. 2020 Sep 1;32(3):353-365.e8. doi: 10.1016/j.cmet.2020.07.002. Epub 2020 Jul 28. PMID: 32726606; PMCID: PMC7501995.
In vivo protocol: 1. Thielen LA, Chen J, Jing G, Moukha-Chafiq O, Xu G, Jo S, Grayson TB, Lu B, Li P, Augelli-Szafran CE, Suto MJ, Kanke M, Sethupathy P, Kim JK, Shalev A. Identification of an Anti-diabetic, Orally Available Small Molecule that Regulates TXNIP Expression and Glucagon Action. Cell Metab. 2020 Sep 1;32(3):353-365.e8. doi: 10.1016/j.cmet.2020.07.002. Epub 2020 Jul 28. PMID: 32726606; PMCID: PMC7501995.

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1: Thielen LA, Chen J, Jing G, Moukha-Chafiq O, Xu G, Jo S, Grayson TB, Lu B, Li P, Augelli-Szafran CE, Suto MJ, Kanke M, Sethupathy P, Kim JK, Shalev A. Identification of an Anti-diabetic, Orally Available Small Molecule that Regulates TXNIP Expression and Glucagon Action. Cell Metab. 2020 Sep 1;32(3):353-365.e8. doi: 10.1016/j.cmet.2020.07.002. Epub 2020 Jul 28. PMID: 32726606; PMCID: PMC7501995.