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.
For research use only. We do not sell to patients.
Name | Trilaciclib hydrochloride (G1T28 hydrochloride) |
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Iupac Chemical Name | 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 dihydrochloride |
Synonyms | Trilaciclib hydrochloride ; G1T28 hydrochloride |
Molecular Formula | C24H32Cl2N8O |
Molecular Weight | 519.47 |
Smile | O=C1NCC2(N3C1=CC4=CN=C(NC5=NC=C(N6CCN(C)CC6)C=C5)N=C43)CCCCC2.[H]Cl.[H]Cl |
InChiKey | BRCYOXKEDFAUSA-UHFFFAOYSA-N |
InChi | InChI=1S/C24H30N8O.2ClH/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);2*1H |
CAS Number | 1977495-97-8 |
Related CAS | 1374743-00-6(Free base) ; 1977495-97-8 (2HCl) |
Packaging | Price | Availability | Purity | Shipping Time |
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Bulk | Enquiry | Enquiry | Enquiry |
Formulation | light-yellow solid to off-white solid |
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Purity | 98% Min. |
Storage | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
Solubility | Soluble in DMSO |
Handling | Avoid inhalation, contact with eyes and skin. Avoid dust and aerosol formation. Use only in areas with appropriate exhaust ventilation. |
Shipping Condition | Shipped under ambient temperature |
HS Code |
Targets | CDK 4/6 INHIBITOR |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study |