SD-208 - Moligand™, ≥98% , Inhibitor of transforming growth factor beta receptor 1, CAS No.627536-09-8, Inhibitor of transforming growth factor beta receptor 1

CAS: 627536-09-8 Cat. No.: S125587 Formula: C17H10ClFN6 Peso molecolare: 352.75 Numero EC: 636-373-7 PubChem CID: 10316032
Disponibile su ordine
QUALITÀ & PUREZZA Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
2-(5-chloro-2-fluorophenyl)-4-(4-pyridylamino)pteridine|2-(5-Chloro-2-fluorophenyl)-4-[(4-pyridyl)amino]pteridine|[2-(5-Chloro-2-fluoro-phenyl)-pteridin-4-yl]-pyridin-4-yl-amine|2-(5-chloro-2-fluoro-phenyl)-N-(4-pyridyl)pteridin-4-amine|2-(5-Chloro-2-fluorophenyl)pteridin-4-yl]pyridin-4-yl-amine|SD208|SD-208|2-(5-chloro-2-fluorophenyl)-N-pyridin-4-ylpteridin-4-amine|2-(5-chloro-2-fluorophenyl)-N-(pyridin-4-yl)pteridin-4-amine|TGF- beta RI Kinase Inhibitor V|2-(5-Chloro-2-fluorophenyl)pteridin-4-yl)pyridin-4-yl amine|SD 208|2-(5-chloro-2-fluorophenyl)-N-4-pyridinyl-4-pteridinamine|4-Pteridinamine, 2-(5-chloro-2-fluorophenyl)-N-4-pyridinyl-|SCI-208
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
5mg
S125587-5mg
—
3 Disponibile

8,59€

12,93€
Salva 4,34 € (33.56%)
25mg
S125587-25mg
—
1 Disponibile

32,02€

48,51€
Salva 16,49 € (33.99%)
100mg
S125587-100mg
—
2 Disponibile

100,57€

150,90€
Salva 50,33 € (33.35%)
Enter a quantity for the sizes you want to add.

Panoramica

SD-208 is a selective TGF-βRI (ALK5) inhibitor with IC50 of 48 nM, >100-fold selectivity over TGF-βRII.
A TGF-β signaling blocker

Specifiche

Sinonimi
2-(5-chloro-2-fluorophenyl)-4-(4-pyridylamino)pteridine | 2-(5-Chloro-2-fluorophenyl)-4-[(4-pyridyl)amino]pteridine | [2-(5-Chloro-2-fluoro-phenyl)-pteridin-4-yl]-pyridin-4-yl-amine | 2-(5-chloro-2-fluoro-phenyl)-N-(4-pyridyl)pteridin-4-amine | 2-(5-Chloro-2-fluorophenyl)pteridin-4-yl]pyridin-4-yl-amine | SD208 | SD-208 | 2-(5-chloro-2-fl Mostra altro
Specifiche e purezza
Moligand™, ≥98%
Meccanismi biochimici e fisiologici
Potent, orally active ATP-competitive transforming growth factor-βreceptor 1 (TGF-βRI) inhibitor (IC50= 49 nM). Displays > 100-fold and > 17-fold selectivity over TGF-βRII and other common kinases respectively. Exhibits anti-inflammatory and antitumor act
Condizioni di conservazione di stoccaggio
Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Grado
Moligand™
Tipo di azione
INHIBITOR
Meccanismo d'azione
Inhibitor of transforming growth factor beta receptor 1
Purezza
≥98%
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
C1=CC(=C(C=C1Cl)C2=NC3=NC=CN=C3C(=N2)NC4=CC=NC=C4)F
IUPAC Name
2-(5-chloro-2-fluorophenyl)-N-pyridin-4-ylpteridin-4-amine
InChIKey
BERLXWPRSBJFHO-UHFFFAOYSA-N
INCHI
1S/C17H10ClFN6/c18-10-1-2-13(19)12(9-10)15-24-16-14(21-7-8-22-16)17(25-15)23-11-3-5-20-6-4-11/h1-9H,(H,20,22,23,24,25)
Isomeri SMILES
C1=CC(=C(C=C1Cl)C2=NC3=NC=CN=C3C(=N2)NC4=CC=NC=C4)F
WGK Germania
3
PubChem CID
10316032
Peso molecolare
352.75

Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassePteridines and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPteridines and derivatives
Alternative Parents Fluorobenzenes  Chlorobenzenes  Aminopyrimidines and derivatives  Aminopyridines and derivatives  Pyrazines  Imidolactams  Aryl fluorides  Aryl chlorides  Heteroaromatic compounds  Azacyclic compounds  Organofluorides  Organochlorides  Hydrocarbon derivatives  Amines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Pteridine - Aminopyridine - Aminopyrimidine - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Imidolactam - Benzenoid - Pyrazine - Pyridine - Pyrimidine - Heteroaromatic compound - Azacycle - Amine - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as pteridines and derivatives. These are polycyclic aromatic compounds containing a pteridine moiety, which consists of a pyrimidine fused to a pyrazine ring to form pyrimido(4,5-b)pyrazine.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
TGFBR1 Tchem TGF-beta receptor type-1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CSNK1D Tchem Casein kinase I delta (4546 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKT2 Tchem Serine/threonine-protein kinase AKT2 (4301 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKT3 Tchem Serine/threonine-protein kinase AKT3 (3157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRKCE Tchem Protein kinase C epsilon (1520 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRKCH Tchem Protein kinase C eta (1863 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRKCQ Tchem Protein kinase C theta (3319 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKT1 Tchem Serine/threonine-protein kinase AKT (9192 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGFBR1 Tchem TGF-beta receptor type I (3786 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MT4 (17854 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U2OS (164939 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRPF1 Tchem Peregrin (2217 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK-293T (167025 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Schistosoma mansoni (6170 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis C virus (23859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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 TypeDataOggetto
E1718066E1718066Certificate of AnalysisJul 07, 2026 S125587
Proprietà chimiche e fisiche
SolubilitàSolvent:DMSO, Max Conc. mg/mL: 7.05, Max Conc. mM: 20 with gentle warming
Indice di rifrazione1.72
Punto di ebollizione (°C)460.41° C at 760 mmHg
Punto di fusione (°C)214.79°C
Peso molecolare352.800 g/mol
XLogP33.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass352.064 Da
Monoisotopic Mass352.064 Da
Topological Polar Surface Area76.500 Ų
Heavy Atom Count25
Formal Charge0
Complexity437.000
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
Domande frequenti e articoli
Calcolatori di soluzioni
Recensioni

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