CX-5279 - Moligand™ , Inhibitor of Pim-1 proto-oncogene; serine/threonine kinase, CAS No.C609627, Inhibitor of Pim-1 proto-oncogene; serine/threonine kinase

CAS: C609627 Cat. No.: C609627 PubChem CID: 72200387
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Storage
Room temperature
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
C609627-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$799.90
25mg
C609627-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$1,714.90
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships 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.

Specifications

Specifications & Purity
Moligand™
Storage
Room temperature
Grade
Moligand™
Action Type
INHIBITOR
Mechanism of action
Inhibitor of Pim-1 proto-oncogene; serine/threonine kinase
Names and Identifiers
Canonical Smiles[O-]C(=O)c1ccc2c(c1)nc(c1c2cnc(n1)NC1CC1)Nc1cccc(c1)C(F)(F)F
IUPAC Name3-(cyclopropylamino)-5-[3-(trifluoromethyl)anilino]pyrimido[4,5-c]quinoline-8-carboxylate
InChIKeyUXZATHOFDZQOMY-UHFFFAOYSA-M
INCHI1S/C22H16F3N5O2/c23-22(24,25)12-2-1-3-14(9-12)27-19-18-16(10-26-21(30-18)28-13-5-6-13)15-7-4-11(20(31)32)8-17(15)29-19/h1-4,7-10,13H,5-6H2,(H,27,29)(H,31,32)(H,26,28,30)/p-1
Isomeric SMILES C1CC1NC2=NC=C3C4=C(C=C(C=C4)C(=O)[O-])N=C(C3=N2)NC5=CC=CC(=C5)C(F)(F)F
PubChem CID 72200387

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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassQuinolines and derivatives
SubclassQuinoline carboxylic acids
Intermediate Tree Nodes Not available
Direct ParentQuinoline carboxylic acids
Alternative Parents Aminoquinolines and derivatives  Trifluoromethylbenzenes  Pyrido[3,4-d]pyrimidines  Aniline and substituted anilines  Aminopyridines and derivatives  Aminopyrimidines and derivatives  Imidolactams  Heteroaromatic compounds  Carboxylic acid salts  Carboxylic acids  Azacyclic compounds  Alkyl fluorides  Organic oxides  Organofluorides  Organooxygen compounds  Amines  Hydrocarbon derivatives  Organic anions  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Quinoline-7-carboxylic acid - Aminoquinoline - Trifluoromethylbenzene - Pyrido[3,4-d]pyrimidine - Aniline or substituted anilines - Aminopyridine - Aminopyrimidine - Monocyclic benzene moiety - Pyridine - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Carboxylic acid salt - Azacycle - Carboxylic acid derivative - Carboxylic acid - Hydrocarbon derivative - Amine - Organofluoride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Alkyl halide - Alkyl fluoride - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organic anion - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PIM1 Tchem Serine/threonine-protein kinase pim-1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Solution Calculators
Reviews

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