TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITH IC50s OF 1 nM AND 4 nM FOR CDK4 AND CDK6, RESPECTIVELY, HAS THE POTENTIAL TO DECREASE MYELOTOXICITY AND IMPROVE ANTI-TUMOR EFFICACY.
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名称 | Trilaciclib (G1T28) |
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Iupac 化学名称 | 2'-((5-(4-methylpiperazin-1-yl)pyridin-2-yl)amino)-7',8'-dihydro-6'H-spiro[cyclohexane-1,9'-pyrazino[1',2':1,5]pyrrolo[2,3-d]pyrimidin]-6'-one |
同义词 | G1T28 ; G1T-28 ; G1T 28 ; Trilaciclib. |
英文同义词 | G1T28 ; G1T-28 ; G1T 28 ; Trilaciclib. |
分子式 | C24H30N8O |
分子量 | 446.559 |
Smile | O=C1NCC2(N3C1=CC4=CN=C(NC5=NC=C(N6CCN(C)CC6)C=C5)N=C43)CCCCC2 |
InChiKey | PDGKHKMBHVFCMG-UHFFFAOYSA-N |
InChi | InChI=1S/C24H30N8O/c1-30-9-11-31(12-10-30)18-5-6-20(25-15-18)28-23-26-14-17-13-19-22(33)27-16-24(7-3-2-4-8-24)32(19)21(17)29-23/h5-6,13-15H,2-4,7-12,16H2,1H3,(H,27,33)(H,25,26,28,29) |
Cas号 | 1374743-00-6 |
相关CAS号 | 1374743-00-6(Free base) ; 1977495-97-8 (2HCl) |
包装 | 价格 | 库存 | 纯度 | 备货期 |
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大货 | 询价 | 询价 | 询价 |
外观性状 | Off-white solid to white solid |
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纯度 | >98% |
存储 | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
可溶性 | Soluble in DMSO |
处理方式 | Avoid inhalation, contact with eyes and skin. Avoid dust and aerosol formation. Use only in areas with appropriate exhaust ventilation. |
运输条件 | Shipped under ambient temperature |
海关编码 | 2933999701 |
Targets | intravenous CDK4/6 inhibitor |
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Mechanism | TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITH IC50s OF 1 nM AND 4 nM FOR CDK4 AND CDK6, RESPECTIVELY, HAS THE POTENTIAL TO DECREASE MYELOTOXICITY AND IMPROVE ANTI-TUMOR EFFICACY. |
Cell study | |
Animal study | |
Clinical study |