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SRT3025 HCl - 99%, high purity , CAS No.2070015-26-6

    Grade & Purity:
  • ≥99%
In stock
Item Number
S414022
Grouped product items
SKU Size
Availability
Price Qty
S414022-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$127.90
S414022-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$576.90
S414022-50mg
50mg
3
$667.90

SIRT1 Selective Inhibitors | Activators | Modulators

Basic Description

Synonyms 4-​Thiazolecarboxamide,5-​(3-​methoxypropyl)​-​2-​phenyl-​N-​[2-​[6-​(1-​pyrrolidinylmethyl)​thiazolo[5,​4-​b]​pyridin-​2-​yl]​phenyl]​-​,hydrochloride (1:1)
Specifications & Purity ≥99%
Biochemical and Physiological Mechanisms SRT3025 is an orally available small molecule activator of the SIRT1 enzyme.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Information

SRT3025 is an orally available small molecule activator of theSIRT1enzyme.


Targets

SIRT1 (Cell-free assay)


In vitro

SRT3025 inhibits RANKL-induced osteoclast differentiation, fusion and resorptive capacity without affecting osteoclast survival. SRT3025 inhibits RANKL-induced osteoclastogenesis in bone marrow-derived macrophages (BMMs) by activating AMPK and deacetylating RelA/p65 lysine 310, critical for activation of the NF-κB signaling pathway. SRT3025 acts faster than oxymetholone to improve hematopoiesis. It does not work by direct activation of Sirt1 in hematopoietic cells. SRT3025 might suppress p21 transcription through the down-regulation of Egr1. SRT3025 is found to activate wild-type Sirt1 protein but failed to activate the E230K mutant, an activation-resistant Sirt1 protein (due to a mutation at position 230).


In vivo

SRT3025 treatment also inhibits tumor growth in Panc-1 xenografts, even though it is not as effective in inhibiting the viability of Panc-1 cells in culture. SRT3025 is well tolerated in mice and has the potential to be used in several diseases. SRT3025 administration expands HSPCs and boosts blood counts while long term SRT3025 administration does not permanently increase or decrease HSC repopulating potential. SRT3025 reduces plasma cholesterol, inflammation, and atherosclerosis in Apoe−/− mice, and it increases hepatic Ldlr expression and Pcsk9 accumulation.


Cell Research(from reference)

Cell lines:HPDE, Panc-1, SU86.86, Patu8988t cells 

Concentrations:0-5 μM 

Incubation Time:72 h 

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Anilides
Intermediate Tree Nodes Not available
Direct Parent Aromatic anilides
Alternative Parents Alpha amino acid amides  Methoxyanilines  Thiazolecarboxamides  Methylpyridines  Aralkylamines  N-alkylpyrrolidines  N-acyl amines  Heteroaromatic compounds  Trialkylamines  Imidothioesters  Sulfenyl compounds  Propargyl-type 1,3-dipolar organic compounds  Imidothioic acids and derivatives  Dialkyl ethers  Carboxylic acid amides  Azacyclic compounds  Aldimines  Organopnictogen compounds  Organic oxides  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Aromatic anilide - Alpha-amino acid amide - Alpha-amino acid or derivatives - Methoxyaniline - Thiazolecarboxylic acid or derivatives - Thiazolecarboxamide - Methylpyridine - Aralkylamine - N-alkylpyrrolidine - Pyridine - N-acyl-amine - Heteroaromatic compound - Thiazole - Pyrrolidine - Azole - Tertiary aliphatic amine - Tertiary amine - Imidothioester - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Imidothioic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid derivative - Aldimine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Hydrochloride - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Imine - Amine - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.
External Descriptors Not available

Product Properties

ALogP 5.849
HBD Count 1
Rotatable Bond 10

Names and Identifiers

IUPAC Name 5-(3-methoxypropyl)-2-phenyl-N-[2-[6-(pyrrolidin-1-ylmethyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]-1,3-thiazole-4-carboxamide;hydrochloride
INCHI InChI=1S/C31H31N5O2S2.ClH/c1-38-17-9-14-26-27(35-29(39-26)22-10-3-2-4-11-22)28(37)33-24-13-6-5-12-23(24)30-34-25-18-21(19-32-31(25)40-30)20-36-15-7-8-16-36;/h2-6,10-13,18-19H,7-9,14-17,20H2,1H3,(H,33,37);1H
InChIKey LGRBDTOIPNDWMN-UHFFFAOYSA-N
Smiles COCCCC1=C(N=C(S1)C2=CC=CC=C2)C(=O)NC3=CC=CC=C3C4=NC5=C(S4)N=CC(=C5)CN6CCCC6.Cl
PubChem CID 118986647
Molecular Weight 606.2

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

1 results found

Lot Number Certificate Type Date Item
G2206399 Certificate of Analysis Apr 03, 2025 S414022

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro DMSO: 100 mg/mL warmed with 50ºC Water: bath (164.96 mM); Ethanol: 5 mg/mL warmed with 50ºC Water: bath (8.24 mM); Water: Insoluble;
Sensitivity Moisture sensitive.
DMSO(mg / mL) Max Solubility 100
DMSO(mM) Max Solubility 164.9620587
Water(mg / mL) Max Solubility <1
Molecular Weight 606.200 g/mol
XLogP3
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 10
Exact Mass 605.169 Da
Monoisotopic Mass 605.169 Da
Topological Polar Surface Area 137.000 Ų
Heavy Atom Count 41
Formal Charge 0
Complexity 811.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Solution Calculators

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