Palbociclib
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Palbociclib
Description:
Palbociclib (PD 0332991) is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respectively. Palbociclib has potent anti-proliferative activity and induces cell cycle arrest in cancer cells, which can be used in the research of HR-positive and HER2-negative breast cancer and hepatocellular carcinoma[1][3][4].Product Name Alternative:
PD 0332991UNSPSC:
12352005Hazard Statement:
H341, H361, H373, H411Target:
CDKType:
Reference compoundRelated Pathways:
Cell Cycle/DNA DamageApplications:
Cancer-Kinase/proteaseField of Research:
CancerAssay Protocol:
https://www.medchemexpress.com/Palbociclib.htmlPurity:
99.97Solubility:
0.1 M HCl : 25 mg/mL (ultrasonic; warming; heat to 60°C) |DMSO : 5 mg/mL (ultrasonic; adjust pH to 5 with HCl)Smiles:
O=C1C (C (C) =O) =C (C2=CN=C (N=C2N1C3CCCC3) NC4=CC=C (N5CCNCC5) C=N4) CMolecular Formula:
C24H29N7O2Molecular Weight:
447.53Precautions:
H341, H361, H373, H411References & Citations:
[1]Fry DW, et al. Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts. Mol Cancer Ther. 2004 Nov;3 (11) :1427-38. |[2]Goel S, et al. CDK4/6 inhibition triggers anti-tumour immunity. Nature. 2017 Aug 24;548 (7668) :471-475. |[3]Richard S Finn, et al. PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro. Breast Cancer Res. 2009;11 (5) :R77. |[4]Bollard J, et al. Palbociclib (PD-0332991), a selective CDK4/6 inhibitor, restricts tumour growth in preclinical models of hepatocellular carcinoma. Gut. 2017 Jul;66 (7) :1286-1296.Shipping Conditions:
Room TemperatureStorage Conditions:
4°C (Powder, protect from light)Scientific Category:
Reference compound1Clinical Information:
LaunchedIsoform:
CDK4; CDK6Citation 01:
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571190-30-2
