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Product Name: | C188-9 | Synonyms: | C188-9;C 188-9;C-188-9;C-1889;C1889;C 1889;C-1889;F0808-0084;N-(1',2-dihydroxy-1.2'-binaphthhalen-4'-yl)-4-methoxybenzene-sulphonamide;C188-9; C 188-9; C-188-9; C-1889; C1889; C 1889; C-1889; F0808-0084;F0808-0084;Benzenesulfonamide, N-(1',2-dihydroxy[1,2'-binaphthalen]-4'-yl)-4-methoxy-;N-(1',2-Dihydroxy-[1,2'-binaphthalen]-4'-yl)-4-methoxybenzenesulfonamide;TTI-101 | CAS: | 432001-19-9 | MF: | C27H21NO5S | MW: | 471.52 | EINECS: | | Product Categories: | | Mol File: | 432001-19-9.mol | ![C188-9 Structure](CAS/20200611/GIF/432001-19-9.gif) |
| C188-9 Chemical Properties |
Boiling point | 680.9±65.0 °C(Predicted) | density | 1.416±0.06 g/cm3(Predicted) | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | solubility | DMF: 10 mg/ml; DMSO: 10 mg/ml; DMSO:PBS (pH 7.2) (1:5): 0.16 mg/ml | form | A crystalline solid | pka | 8.14±0.50(Predicted) | color | Off-white to pink |
| C188-9 Usage And Synthesis |
Biological Activity | C188-9 (TTI 101) is a potent STAT3 inhibitor, binds STAT3 with high affinity, Kd=4.7±0.4 nM. It is well tolerated in mice, has good oral bioavailability, and is mainly enriched in tumor tissues. | in vitro | C188-9 is a small molecule inhibitor of STAT3, targeting the phosphotyrosine peptide binding site in the SH2 region of STAT3 with a Ki value of 136 nM. It does not inhibit upstream Jak or Src kinases. | in vivo | C188-9 inhibited tumor growth in mice bearing UM-SCC-17B xenografts after administration of C188-9. C188-9 was well tolerated in mice, had good oral bioavailability, and was concentrated in tumor tissue after administration. | target | Target | Value | STAT3 (Cell-free) | 4.7 nM(Kd) |
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| C188-9 Preparation Products And Raw materials |
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