ASP4132 - ≥98% , CAS No.1640294-30-9

CAS: 1640294-30-9 Cat. No.: A414292 Molecular Weight: 937.06 PubChem CID: 146673134
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
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 -20°C
Shipped In
Ice chest + Ice pads
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Size
Status
Price
Qty
1mg
A414292-1mg
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$57.90
5mg
A414292-5mg
3
$205.90
25mg
A414292-25mg
3
$675.90
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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.

Overview

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

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)
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
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.
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
ACTIVATOR
Purity
≥98%
Product Properties
ALogP8.594
HBD Count1
Rotatable Bond10
Names and Identifiers
Pubchem Sid504773628
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504773628
Canonical SmilesCC1=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)
Isomeric SMILES 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
Molecular Weight 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
ClassPiperidines
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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
MDA-MB-453 (1139 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-BR-3 (5175 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

2 results found

Lot NumberCertificate TypeDateItem
J2214765Certificate of AnalysisJul 10, 2025 A414292
J2214770Certificate of AnalysisJul 10, 2025 A414292
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 100 mg/mL (106.71 mM); Water: Insoluble; Ethanol: Insoluble;
DMSO(mg / mL) Max Solubility100
DMSO(mM) Max Solubility106.716752395791
Water(mg / mL) Max Solubility<1
Molecular Weight937.100 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
Solution Calculators
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