(S)-ROSCOVITINE
(S)-ROSCOVITINE Basic information
- Product Name:
- (S)-ROSCOVITINE
- Synonyms:
-
- (2S)-2-[[9-(1-Methylethyl)-6-[(phenylmethyl)amino]-9H-purin-2-yl]amino]-1-butanol
- Roscovitine, (S)-Isomer - CAS 186692-45-5 - Calbiochem
- 1-Butanol, 2-[[9-(1-methylethyl)-6-[(phenylmethyl)amino]-9H-purin-2-yl]amino]-, (2S)-
- CAS:
- 186692-45-5
- MF:
- C19H26N6O
- MW:
- 354.45
- Mol File:
- 186692-45-5.mol
(S)-ROSCOVITINE Chemical Properties
- Melting point:
- 103-106℃
- Density
- 1.25
- storage temp.
- -20C
- form
- White solid
- color
- White to off-white
(S)-ROSCOVITINE Usage And Synthesis
Uses
(S)-Roscovitine ((S)-Seliciclib; (S)-CYC202) is a potent and cross the blood-brain barrier CDKs inhibitor. (S)-Roscovitine shows neuroprotective efficacy. (S)-Roscovitine has the potential for the research of stroke[1][2].
in vivo
(S)-Roscovitine (25 mg/kg; i.p.; 15 min before and 1 hr after pMCAo) shows neuroprotective efficacy in an adult mouse model of permanent MCAo (middle cerebral artery occlusion) [2].
| Animal Model: | 20-25 g, P60 male C57 b/6 mice[2] |
| Dosage: | 25 mg/kg |
| Administration: | I.p.; at 15 min before and 1 hr after pMCAo |
| Result: | Decreased of the total infarct volume. |
IC 50
CDK1: ≤1 μM (IC50); CDK2: ≤1 μM (IC50); CDK5: ≤1 μM (IC50); CDK7: ≤1 μM (IC50); CDK9: ≤1 μM (IC50)
storage
+4°C
References
[1] Le Roy L, et al. Cellular and Molecular Mechanisms of R/S-Roscovitine and CDKs Related Inhibition under Both Focal and Global Cerebral Ischemia: A Focus on Neurovascular Unit and Immune Cells. Cells. 2021 Jan 8;10(1):104. DOI:10.3390/cells10010104
[2] Menn B, et al. Delayed treatment with systemic (S)-roscovitine provides neuroprotection and inhibits in vivo CDK5 activity increase in animal stroke models. PLoS One. 2010 Aug 12;5(8):e12117. DOI:10.1371/journal.pone.0012117
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