TP0427736 HCl - 10mM in DMSO , CAS No.864374-00-5

CAS: 864374-00-5 Cat. No.: T426429 Formule: C14H11ClN4S2 Poids moléculaire: 334.85 PubChem CID: 136105618
DISPONIBLE À COMMANDE
GRADE & PURITY 10mM in DMSO
Synonyms
6-​[5-​(4-​methyl-​2-​thiazolyl)​-​1H-​imidazol-​4-​yl]​-Benzothiazole hydrochloride
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Allemagne (EU)
USA*
Price
Qty
1ml
T426429-1ml
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2 En stock

143,09€

209,91€
Enregistrer 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Information

TP0427736 is a potent inhibitor ofALK5 kinase activitywith anIC50of 2.72 nM and this effect is 300-fold higher than the inhibitory effect on ALK3 (IC50 = 836 nM for ALK3). It also inhibits Smad2/3 phosphorylation in A549 cells induced by TGF-β1 with an IC50 value of 8.68 nM.

Targets

ALK5 (Cell-free assay) 2.72 nM

In vitro

TP0427736 inhibits Smad2/3 phosphorylation in a concentration-dependent manner, with an IC50 value of 8.68 nM. In a cell-based assay of outer root sheath cells, TP0427736 rescued the inhibited proliferation by TGF-β1 and TGF-β2 in a concentration-dependent manner.

In vivo

TP0427736 decreases shortening of hair follicle length during the transition from the late anagen phase to the catagen phase.

Cell Research(from reference)

Cell lines:A549 cells 

Incubation Time:2 h 

Specifications

Synonymes
6-​[5-​(4-​methyl-​2-​thiazolyl)​-​1H-​imidazol-​4-​yl]​-Benzothiazole hydrochloride
Spécifications et pureté
10mM in DMSO
Mécanismes biochimiques et physiologiques
TP0427736 is a potent inhibitor of ALK5 kinase activity with an IC50 of 2.72 nM and this effect is 300-fold higher than the inhibitory effect on ALK3 (IC50 = 836 nM for ALK3). It also inhibits Smad2/3 phosphorylation in A549 cells induced by TGF-β1 with a
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Propriétés du produit
ALogP
3.084
Nombre de HBD
1
Liaison rotative
2
Noms et identifiants
Pubchem Sid
Sourires canoniques
CC1=CSC(=N1)C2=C(N=CN2)C3=CC4=C(C=C3)N=CS4
IUPAC Name
6-[5-(4-methyl-1,3-thiazol-2-yl)-1H-imidazol-4-yl]-1,3-benzothiazole
InChIKey
LLFCXRYULHMNCG-UHFFFAOYSA-N
INCHI
1S/C14H10N4S2/c1-8-5-19-14(18-8)13-12(15-6-16-13)9-2-3-10-11(4-9)20-7-17-10/h2-7H,1H3,(H,15,16)
Isomères SMILES
CC1=CSC(=N1)C2=C(N=CN2)C3=CC4=C(C=C3)N=CS4
PubChem CID
136105618
Poids moléculaire
334.85

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.

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
ClasseBenzothiazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzothiazoles
Alternative Parents 2,4-disubstituted thiazoles  Benzenoids  Imidazoles  Heteroaromatic compounds  Azacyclic compounds  Organonitrogen compounds  Hydrocarbon derivatives  Organic anions  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 1,3-benzothiazole - 2,4-disubstituted 1,3-thiazole - Benzenoid - Heteroaromatic compound - Thiazole - Imidazole - Azole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic anion - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzothiazoles. These are organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
TGFBR1 Tchem TGF-beta receptor type-1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TGFBR1 Tchem TGF-beta receptor type I (3786 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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 NumberCertificate TypeDateArticle
F2403398Certificate of AnalysisApr 03, 2026 T426429
Propriétés chimiques et physiques
DMSO (mg/mL) Solubilité maximale67
DMSO (mM) Solubilité maximale200.089592354786
Eau (mg/mL) Solubilité maximale<1
Poids moléculaire298.400 g/mol
XLogP33.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count2
Exact Mass298.035 Da
Monoisotopic Mass298.035 Da
Topological Polar Surface Area111.000 Ų
Heavy Atom Count20
Formal Charge0
Complexity356.000
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 Count1
Citations of This Product
Calculateurs de solution
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