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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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S126125-10mg | 10mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $155.90 | |
S126125-50mg | 50mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $469.90 |
Potent, reversible, competitive ALK5 inhibitor
Synonyms | HMS3655F08 | SCHEMBL373422 | AS-74679 | amino-4,6-dimethoxypyrimidine | CCG-267861 | TGF-beta RI Inhibitor III | ethoxycarbonylacetylchloride | 2-(5-(Benzo[d][1,3]dioxol-5-yl)-2-(tert-butyl)-1H-imidazol-4-yl)-6-methylpyridine | SB 505124 | 2-[4-(1,3-Benzo |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | SB-505124 is an inhibitor of activin receptor-like kinase (ALK-5). SB-505124 is demonstrated to suppress the action of transforming growth factor-B (TGF-B) both in vitro and in vivo.Potent, reversible, competitive ALK5 inhibitor (IC 50 values are 47 and 1 |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of transforming growth factor beta receptor 1 |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5 with IC50 of 129 nM and 47 nM in cell-free assays, respectively, also inhibits ALK7, but does not inhibit ALK1, 2, 3, or 6. |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 2-[4-(1,3-benzodioxol-5-yl)-2-tert-butyl-1H-imidazol-5-yl]-6-methylpyridine |
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INCHI | InChI=1S/C20H21N3O2/c1-12-6-5-7-14(21-12)18-17(22-19(23-18)20(2,3)4)13-8-9-15-16(10-13)25-11-24-15/h5-10H,11H2,1-4H3,(H,22,23) |
InChi Key | WGZOTBUYUFBEPZ-UHFFFAOYSA-N |
Canonical SMILES | CC1=NC(=CC=C1)C2=C(N=C(N2)C(C)(C)C)C3=CC4=C(C=C3)OCO4 |
Isomeric SMILES | CC1=NC(=CC=C1)C2=C(N=C(N2)C(C)(C)C)C3=CC4=C(C=C3)OCO4 |
PubChem CID | 9858940 |
Molecular Weight | 335.4 |
PubChem CID | 9858940 |
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ChEMBL Ligand | CHEMBL226838 |
CAS Registry No. | 694433-59-5 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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H1506110 | Certificate of Analysis | Mar 16, 2023 | S126125 |
Solubility | DMSO 67 mg/mL Water <1 mg/mL Ethanol 67 mg/mL |
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Melt Point(°C) | 168 °C |
1. Jin CH, Sreenu D, Krishnaiah M, Subrahmanyam VB, Rao KS, Nagendra Mohan AV, Park CY, Son JY, Son DH, Park HJ et al.. (2011) Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin-2-yl)-4-(quinoxalin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors.. Eur J Med Chem, 46 (9): (3917-25). [PMID:21696866] |
2. Bui AT et al.. (2015) SMAD signaling and redox imbalance cooperate to induce prostate cancer cell dormancy.. Cell Cycle, 14 (8): (1218-31). [PMID:25706341] |
3. Bui AT et al.. (2017) Transient exposure to androgens induces a remarkable self-sustained quiescent state in dispersed prostate cancer cells.. Cell Cycle, 16 (9): (879-893). [PMID:28426320] |