TIMTEC-BB SBB005393
TIMTEC-BB SBB005393 Basic information
- Product Name:
- TIMTEC-BB SBB005393
- Synonyms:
-
- TIMTEC-BB SBB005393
- (2,4-Dichlorophenyl)carbamimidothioic acid methyl ester hydrochloride
- 2-(2,4-Dichlorobenzyl)-2-thiopseudourea hydrochloride
- Rb/Raf-1 disruptor 251 hydrochloride
- RRD-251 hydrochloride
- S-(2,4-Dichlorobenzyl)-isothiouronium hydrochloride
- (2,4-dichlorophenyl)methylsulfanylformamidine hydrochloride
- (2,4-dichlorophenyl)methylsulfanylmethanimidamide hydrochloride
- CAS:
- 72214-67-6
- MF:
- C8H9Cl3N2S
- MW:
- 271.6
- Mol File:
- 72214-67-6.mol
TIMTEC-BB SBB005393 Chemical Properties
- Melting point:
- 222-227 °C
- storage temp.
- room temp
- solubility
- DMSO: >10mg/mL
- form
- White solid
- color
- white to off-white
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26
- WGK Germany
- 3
- HS Code
- 2930909899
TIMTEC-BB SBB005393 Usage And Synthesis
Uses
RRD-251 Hydrochloride is a reversible selective disruptor of Rb-Raf-1 interaction.
Biological Activity
RRD-251 hydrochloride is a reversible, potent, and selective disruptor of Rb/Raf-1 interaction. The retinoblastoma tumor suppressor protein (Rb) controls the G1-S boundary by repressing the transcriptional activity of the E2F family of transcription factors. Raf-1 kinase binds and phosphorylates Rb early in the G1 phase. RRD-251 significantly inhibits angiogenesis and tumor growth in vivo in an Rb-dependent manner. RRD-251 does not inhibit the binding of B-Raf to Rb and Raf-1 to Mek1/2. Also, RRD-251 does not affect the kinase activities associated with cyclin D, cyclin E, or Raf-1.
in vivo
RRD-251 (50 mg/kg; i.p.; q.o.d; for 14 days) has anti-cancer activities in vivo on melanomas[1].
| Animal Model: | 8-wk-old female athymic nude mice, with SK-ME-28 xenograft[1] |
| Dosage: | 50 mg/kg |
| Administration: | Intraperitoneal administration, qod, for 14 days |
| Result: | Inhibits the growth of SK-ME-28 xenograft in nude mice. |
TIMTEC-BB SBB005393Supplier
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