ASP4132 - 10mM in DMSO , CAS No.1640294-30-9

CAS: 1640294-30-9 Cat. No.: A422025 Fórmula: C46H51F3N6O8S2 Peso molecular: 937.06 PubChem CID: 146673134
Disponível para encomenda
GRADE & PURITY 10mM in DMSO
Synonyms
Methanone,[6-​[1-​[(6-​methoxy-​3-​pyridinyl)​methyl]​-​4-​piperidinyl]​-​1H-​benzimidazol-​2-​yl]​[4-​[[4-​(trifluoromethyl)​phenyl]​methyl]​-​1-​piperazinyl]​-​,4-​methylbenzenesulfona​te (1:2)
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Alemanha (EU)
USA*
Price
Qty
1ml
A422025-1ml
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2 Em stock

143,09€

209,91€
Gravar 66,82 € (31.83%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

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

Visão geral

Information

ASP4132 ASP4132 is a potent and orally active activator of Adenosine Monophosphate-Activated Protein Kinase (AMPK) with EC50 of 0.018 μM. ASP4132 is used as a clinical candidate for the treatment of human cancer.

Targets

AMPK (Cell-free assay) 0.018 μM(EC50)

In vitro

ASP4132 is a new type of AMPK activator with potent AMPK activation activity and attractive selective growth inhibition against human cancer cells, improves aqueous solubility, metabolic stability and animal pharmacokinetics (PK). Studies on ASP4132 have advanced to clinical trials for the treatment of cancer.

In vivo

The in vivo efficacy of ASP4132 is evaluated via MDA-MB-453 xenografts in nude mice. The tumor growth inhibition (TGI) rate is 29% at 1 mg/kg (p.o.), and the tumor regression rate is 26%, 87% and 96% at 2, 4 and 8 mg/kg, respectively. All doses of ASP4132 are well tolerated over the 21-day dosing window, and no body weight loss is observed.

Cell Research(from reference)

Cell lines:MDA-MB-453, SK-BR-3, AU565, OCUB-M, 

Concentrations:0.3 nM, 1 nM, 3 nM, 10 nM, 30 nM, 100 nM, 300 nM, 1000 nM, 3000 Nm 

Incubation Time:2 h, 4 days 

Specifications

Sinónimos
Methanone,[6-​[1-​[(6-​methoxy-​3-​pyridinyl)​methyl]​-​4-​piperidinyl]​-​1H-​benzimidazol-​2-​yl]​[4-​[[4-​(trifluoromethyl)​phenyl]​methyl]​-​1-​piperazinyl]​-​,4-​methylbenzenesulfona​te (1:2)
Especificações e pureza
10mM in DMSO
Mecanismos bioquímicos e fisiológicos
ASP4132 is a potent and orally active activator of Adenosine Monophosphate-Activated Protein Kinase (AMPK) with EC50 of 0.018 μM. ASP4132 is used as a clinical candidate for the treatment of human cancer.
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Tipo de ação
ACTIVATOR
Propriedades do produto
ALogP8.594
Contagem HBD1
Ligação rotativa10
Nomes e identificadores
Pubchem Sid528763158
Sorrisos canónicosCC1=CC=C(C=C1)S(=O)(=O)O.CC1=CC=C(C=C1)S(=O)(=O)O.COC1=NC=C(C=C1)CN2CCC(CC2)C3=CC4=C(C=C3)N=C(N4)C(=O)N5CCN(CC5)CC6=CC=C(C=C6)C(F)(F)F
IUPAC Name[6-[1-[(6-methoxypyridin-3-yl)methyl]piperidin-4-yl]-1H-benzimidazol-2-yl]-[4-[[4-(trifluoromethyl)phenyl]methyl]piperazin-1-yl]methanone;4-methylbenzenesulfonic acid
InChIKeyKDMGCEXVMOJAAC-UHFFFAOYSA-N
INCHI1S/C32H35F3N6O2.2C7H8O3S/c1-43-29-9-4-23(19-36-29)21-39-12-10-24(11-13-39)25-5-8-27-28(18-25)38-30(37-27)31(42)41-16-14-40(15-17-41)20-22-2-6-26(7-3-22)32(33,34)35;2*1-6-2-4-7(5-3-6)11(8,9)10/h2-9,18-19,24H,10-17,20-21H2,1H3,(H,37,38);2*2-5H,1H3,(H,8,9,10)
SMILES isoméricas CC1=CC=C(C=C1)S(=O)(=O)O.CC1=CC=C(C=C1)S(=O)(=O)O.COC1=NC=C(C=C1)CN2CCC(CC2)C3=CC4=C(C=C3)N=C(N4)C(=O)N5CCN(CC5)CC6=CC=C(C=C6)C(F)(F)F
PubChem CID 146673134
Peso molecular 937.06

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
ClassePiperidines
SubclassPhenylpiperidines
Intermediate Tree Nodes Not available
Direct ParentPhenylpiperidines
Alternative Parents p-Methylbenzenesulfonates  Trifluoromethylbenzenes  Tosyl compounds  Benzimidazoles  Benzenesulfonyl compounds  1-sulfo,2-unsubstituted aromatic compounds  Phenylmethylamines  Benzylamines  2-heteroaryl carboxamides  N-alkylpiperazines  Aralkylamines  Alkyl aryl ethers  Pyridines and derivatives  Tertiary carboxylic acid amides  Sulfonyls  Organosulfonic acids  Imidazoles  Heteroaromatic compounds  Trialkylamines  Amino acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organofluorides  Organic oxides  Hydrocarbon derivatives  Alkyl fluorides  
Molecular FrameworkNot available
Substituents Phenylpiperidine - P-methylbenzenesulfonate - Trifluoromethylbenzene - Tosyl compound - Benzenesulfonate - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Benzimidazole - Arylsulfonic acid or derivatives - 2-heteroaryl carboxamide - Phenylmethylamine - Benzylamine - Aralkylamine - N-alkylpiperazine - Toluene - Alkyl aryl ether - Benzenoid - Pyridine - Piperazine - 1,4-diazinane - Monocyclic benzene moiety - Heteroaromatic compound - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Imidazole - Azole - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Amino acid or derivatives - Azacycle - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Amine - Alkyl halide - Alkyl fluoride - Aromatic heteropolycyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as phenylpiperidines. These are compounds containing a phenylpiperidine skeleton, which consists of a piperidine bound to a phenyl group.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
MDA-MB-453 (1139 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-BR-3 (5175 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
DMSO (mg/mL) Solubilidade máxima100
DMSO (mM) Solubilidade máxima106.716752395791
Água (mg/mL) Solubilidade máxima<1
Peso molecular937.100 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count15
Rotatable Bond Count9
Exact Mass936.316 Da
Monoisotopic Mass936.316 Da
Topological Polar Surface Area203.000 Ų
Heavy Atom Count65
Formal Charge0
Complexity1110.000
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 Count3
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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