SKF-34288 hydrochloride - ≥95% , CAS No.320386-54-7

CAS: 320386-54-7 Cat. No.: S650474 Peso molecular: 191.64 PubChem CID: 24721311
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
FT-0671101 | 3-sulfanylpyridine-2-carboxylic acid;hydrochloride | AS-79457 | D94966 | AKOS027321159 | SKF-34288 hydrochloride | A904188 | HY-128923 | SKF-34288 (hydrochloride) | 3-Mercaptopicolinic acid (hydrochloride) | J-018609 | 3-Mercaptopicolinic Aci
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
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Size
Estado
Price
Qty
1mg
S650474-1mg
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9,90US$

14,90US$
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5mg
S650474-5mg
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21,90US$

32,90US$
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10mg
S650474-10mg
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32,90US$

49,90US$
Guardar 17,00 US$ (34.07%)
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Desiccated Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

SKF-34288 (3-Mercaptopicolinic acid) hydrochloride is an orally active phosphoenolpyruvate carboxykinase ( PEPCK ) inhibitor ( K i : 2-9 μM). SKF-34288 hydrochloride is a potent hypoglycemic agent by inhibiting glucose synthesis. SKF-34288 hydrochloride also inhibits Asn metabolism and increases amino acids and amides

In Vitro

SKF-34288 hydrochloride (0.01-1 mM, 48 h) inhibits C2C12 cell proliferation . SKF-34288 hydrochloride (0.25-1 mM, 0-5 day) induces myogenic differentiation of C2C12 cells . SKF-34288 hydrochloride (0.25 or 1 mM) reduces mRNA expression of Pck2 and genes associated with serine biosynthesis . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay Cell Line: C2C12 cell Concentration: 0, 0.01, 0.1, 0.25, 0.5, 1 mM Incubation Time: 48 h Result: Dose-dependently inhibited C2C12 cell proliferation.

In Vivo

SKF-34288 hydrochloride (37.5-150mg/kg, p.o.) reduces blood glucose in starved rats . SKF-34288 hydrochloride (25 mg/kg, s.c.) neutralizes Salbutamol- mediated hyperglycaemia in rabbits. SKF-34288 hydrochloride (30 and 300 mg/kg, i.p.) reduces Pyruvate-induced blood glucose level in rats. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Starved rats Dosage: 37.5, 75 and 150mg/kg Administration: Oral administration (p.o.) Result: Showed dose-dependent magnitude and duration of the hypoglycaemic effect.

Form:Solid

IC50& Target:Ki: 2-9 μM (PEPCK)

Specifications

Sinónimos
FT-0671101 | 3-sulfanylpyridine-2-carboxylic acid;hydrochloride | AS-79457 | D94966 | AKOS027321159 | SKF-34288 hydrochloride | A904188 | HY-128923 | SKF-34288 (hydrochloride) | 3-Mercaptopicolinic acid (hydrochloride) | J-018609 | 3-Mercaptopicolinic Aci
Especificaciones y pureza
≥95%
Mecanismos bioquímicos y fisiológicos
SKF-34288 (3-Mercaptopicolinic acid) hydrochloride is an orally active phosphoenolpyruvate carboxykinase ( PEPCK ) inhibitor ( K i : 2-9 μM). SKF-34288 hydrochloride is a potent hypoglycemic agent by inhibiting glucose synthesis. SKF-34288 hydrochloride a
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasC1=CC(=C(N=C1)C(=O)O)S.Cl
IUPAC Name3-sulfanylpyridine-2-carboxylic acid;hydrochloride
InChIKeyDYGYEUUVNLEHJP-UHFFFAOYSA-N
INCHI1S/C6H5NO2S.ClH/c8-6(9)5-4(10)2-1-3-7-5;/h1-3,10H,(H,8,9);1H
Isómeros SMILES C1=CC(=C(N=C1)C(=O)O)S.Cl
PubChem CID 24721311
Peso molecular 191.64

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasePyridines and derivatives
SubclassPyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentPyridinecarboxylic acids
Alternative Parents Heteroaromatic compounds  Carboxylic acids  Azacyclic compounds  Thiols  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrochlorides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyridine carboxylic acid - Heteroaromatic compound - Azacycle - Arylthiol - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Hydrochloride - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadH2O : 5 mg/mL (26.09 mM; Need ultrasonic)
Peso molecular191.640 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass190.981 Da
Monoisotopic Mass190.981 Da
Topological Polar Surface Area51.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity140.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calculadoras de soluciones
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