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(S)-Roscovitine
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Catalog No. T88822Cas No. 186692-45-5
Alias (S)-Seliciclib, (S)-CYC202
(S)-Roscovitine ((S)-Seliciclib; (S)-CYC202) is a potent inhibitor of CDKs capable of crossing the blood-brain barrier. It exhibits neuroprotective effects and holds potential for use in stroke research.
(S)-Roscovitine
😃Good
Catalog No. T88822Alias (S)-Seliciclib, (S)-CYC202Cas No. 186692-45-5
(S)-Roscovitine ((S)-Seliciclib; (S)-CYC202) is a potent inhibitor of CDKs capable of crossing the blood-brain barrier. It exhibits neuroprotective effects and holds potential for use in stroke research.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 25 mg | $1,520 | 4-6 weeks | |
| 50 mg | $1,980 | 4-6 weeks | |
| 100 mg | $2,500 | 4-6 weeks |
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Product Introduction
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Chemical Properties
| Description | (S)-Roscovitine ((S)-Seliciclib; (S)-CYC202) is a potent inhibitor of CDKs capable of crossing the blood-brain barrier. It exhibits neuroprotective effects and holds potential for use in stroke research. |
| Targets&IC50 | CDK7:≤1 μM, CDK2:≤1 μM, CDK5:≤1 μM, CDK9:≤1 μM, CDK1:≤1 μM |
| In vivo | In an animal model study using 20-25 g, P60 male C57 b/6 mice, '(S)-Roscovitine' (25 mg/kg; i.p.; administered 15 minutes before and 1 hour after permanent middle cerebral artery occlusion [pMCAo]) demonstrated neuroprotective effects. The treatment resulted in a reduction of the total infarct volume in this model. |
| Synonyms | (S)-Seliciclib, (S)-CYC202 |
| Molecular Weight | 354.45 |
| Formula | C19H26N6O |
| Cas No. | 186692-45-5 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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