ChemicalBook >> CAS DataBase List >>SRT1720

SRT1720

CAS No.
1001645-58-4
Chemical Name:
SRT1720
Synonyms
CS-233;SRT1720;STR1720;Span 55;CAY10559;CAY-10559;SIRT 1933;SIRT-1933;SIRT1933.;CAY 10559
CBNumber:
CB32512407
Molecular Formula:
C25H24ClN7OS
Molecular Weight:
506.03
MDL Number:
MFCD18074509
MOL File:
1001645-58-4.mol
MSDS File:
SDS
Last updated:2023-05-18 11:31:10

SRT1720 Properties

Melting point >205°C (dec.)
Density 1.58
storage temp. = -70C
solubility Soluble in DMSO (>25 mg/ml)
form Liquid
color White
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338

SRT1720 price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 5.30748 InSolution SRT1720, HCl - CAS 1001645-58-4 - Calbiochem A 25 mM (10 mg/650 μl) sterile-filtered solution of SRT1720, HCl in DMSO. 1001645-58-4 10MG $264 2024-03-01 Buy
Cayman Chemical 10011020 SRT 1720 (hydrochloride) ≥98% 1001645-58-4 1mg $39 2024-03-01 Buy
Cayman Chemical 10011020 SRT 1720 (hydrochloride) ≥98% 1001645-58-4 5mg $126 2024-03-01 Buy
Cayman Chemical 10011020 SRT 1720 (hydrochloride) ≥98% 1001645-58-4 10mg $210 2024-03-01 Buy
Cayman Chemical 10011020 SRT 1720 (hydrochloride) ≥98% 1001645-58-4 50mg $847 2024-03-01 Buy
Product number Packaging Price Buy
5.30748 10MG $264 Buy
10011020 1mg $39 Buy
10011020 5mg $126 Buy
10011020 10mg $210 Buy
10011020 50mg $847 Buy

SRT1720 Chemical Properties,Uses,Production

Description

SRT1720 is a selective SIRT1 activator with EC50 of 0.16 μM in a cell-free assay, but is >230-fold less potent for SIRT2 and SIRT3.

In vitro

The maximum activation ratio of SRT1720 versus the closest sirtuin homologues, SIRT2 (EC1.5 = 37 μM) and SIRT3 (EC1.5 > 300 μM) is up to 781%. SRT1720 binds to the SIRT1 enzyme-peptide substrate complex at an allosteric site amino-terminal to the catalytic domain and lower the Michaelis constant for acetylated substrates. SRT1720 could reduce fed glucose levels. Glucose excursion during an intraperitoneal glucose tolerance test is also significantly reduced in the SRT1720 group, and comparable to rosiglitazone, a PPARγ activator that has been used to treat type 2 diabetes. SRT1720 does not have an effect on fasting glucose in chow-fed mice, revealing that pharmacological SIRT1 activation is unlikely to induce hypoglycaemia. SRT1720 significantly reduces the hyperinsulinaemia after 4 weeks, partially normalizing increased insulin levels similar to rosiglitazone treatment. SRT1720 treatment increases mitochondrial capacity by 15% in gastrocnemius muscle as measured by citrate synthase activity. Higher concentrations of SRT1720 (15 μM) induces a modest (10-20%) decrease in normal cell viability. SRT1720 also significantly inhibits VEGF-dependent MM cell migration.

In vivo

In DIO mice SRT1720 mimics several of the effects observed after calorie restriction including improved insulin sensitivity, normalized glucose and insulin levels, and increased mitochondrial capacity. In addition, in diet-induced obese and genetically obese mice, SRT1720 improves insulin sensitivity, lower plasma glucose, and increase mitochondrial capacity. Thus, SRT1720 is a promising new therapeutic agent for treating diseases of ageing such as type 2 diabetes. Consistent with improved glucose tolerance, the glucose infusion rate required to maintain euglycaemia is approximately 35% higher in SRT1720-treated fa/fa rats, and the total glucose disposal rate is increased by approximately 20%. SRT1720 also prevents multiple myeloma tumor growth. SRT1720 increases the cytotoxic activity of bortezomib or dexamethasone.

References

http://www.selleckchem.com/products/SRT1720.html

Description

SRT1720 (1001645-58-4) is a SIRT1 activator (EC1.5 = 0.16 μM, max activation = 781%).1 It reduced glucose levels and hyperinsulinemia in DIO, Lepob/ob mice and Zucker fa/fa rats.? SRT1720 enhanced endurance running and protected against diet-induced obesity and insulin resistance via enhancement of oxidative metabolism in skeletal muscle, liver, and brown adipose tissue.2 It induced mitochondrial biogenesis in oxidant-induced renal proximal tube cell injury.3 SRT1720 repressed circadian clock gene expression and decreased H3 K9/K14 acetylation in a time-specific manner.4 It attenuated angiotensin II-induced atherosclerosis by inhibiting the vascular inflammatory response.5

Uses

SRT1720 acts as a therapeutic in the treatment of type 2 diabetes. It modulates calories and contributes to glucose homeostasis and insulin sensitivity.

General Description

An enhanced aqueous soluble version of SRT1720 (Cat. No. 567860).

Biochem/physiol Actions

Cell permeable: yes

target

SIRT1

References

Milne et al. (2007), Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes; Nature 450 712 Feige et al. (2008), Specific SIRT1 activation mimics low energy levels and protects against diet-induced metabolic disorders by enhancing fat oxidation; Cell Metab. 8 347 Funk et al. (2010), SRT1720 induces mitochondrial biogenesis and rescues mitochondrial function after oxidant injury in renal proximal tubule cells; J. Pharmacol. Exp. Ther. 333 593 Bellet et al. (2013), Pharmacological modulation of circadian rhythms by synthetic activators of the deacetylase SIRT1; Proc. Natl. Acad. Sci. USA 110 3333 Chen et al. (2015), The Sirt1 activator SRT1720 attenuates angiotensin II-induced atherosclerosis in apoE-/- mice through inhibiting vascular inflammatory response; Biochem. Biophys. Res. Commun. 465 732

SRT1720 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 166)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9339 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32715 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49391 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58

View Lastest Price from SRT1720 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
SRT1720 pictures 2019-07-06 SRT1720
1001645-58-4
US $1000.00 / KG 1G 99% 100kg Career Henan Chemical Co
  • SRT1720 pictures
  • SRT1720
    1001645-58-4
  • US $1000.00 / KG
  • 99%
  • Career Henan Chemical Co

SRT1720 Spectrum

N-(2-(3-(piperazin-1-ylMethyl)iMidazo[2,1-b]thiazol-6-yl)phenyl)quinoxaline-2-carboxaMide hydrochloride SRT1720 N-[2-[3-(1-Piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl]phenyl]-2-quinoxalinecarboxamide hydrochloride SRT1720HCL SRT 1720 (Hydrochloride) N-[2-[3-(1-Piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl]phenyl]-2-quinoxalinecarboxamide hydrochloride SRT 1720 SRT-1720 xhydrochloride SRT1720 hydrochloride, >=98% SRT 1720 tetrahydrochloride SRT1720;SRT-1720 N-(2-(3-(Piperazin-1-ylmethyl)imidazo[2,1-b]thiazol-6-yl)phenyl)quinoxaline-2-carboxamide hydr CAY10559 CAY-10559 SIRT 1933 SIRT-1933 SIRT1933. SRT-1720 HCl, SRT-1720 hydrochloride SRT-1720 HCL, SRT-1720 HYDROCHLORIDE; SRT1720; SRT-1720; SRT 1720; CAY10559; CAY-10559; CAY 10559; SIRT-1933; SIRT 1933; SIRT1933. N-[2-[3-(piperazin-1-ylmethyl)imidazo[2,1-b][1,3]thiazol-6-yl]phenyl]quinoxaline-2-carboxamide,hydrochloride STR1720 CS-233 SRT1720 USP/EP/BP SRT1720 HCL (CAY-10559) Emsorb 2505 Liposorb S-20 Sorbon S 60 Span 55 CAY 10559 N-(2-(3-(Piperazin-1-ylmethyl)imidazo[2,1-b]thiazol-6-yl)phenyl)quinoxaline-2-carboxamide xhydrochloride SRT-1720 HCl SRT1720 HCl SRT-1720 hydrochloride,SRT1720 hydrochloride 1001645-58-4 C25H23N7OSHCl C25H24ClN7OS Inhibitor Inhibitors