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Product details:
CAS
571190-30-2
Purity
95%
Palbociclib is an endocrine-based chemotherapeutic agent used to treat HER2-negative and HR-positive advanced or metastatic breast cancer.
Properties
Name
Palbociclib
Smiles
CC(=O)C1=C(C)C=2C=NC(NC=3C=CC(=CN3)N4CCNCC4)=NC2N(C5CCCC5)C1=O
Targets
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Sold for research purposes under agreement from Pfizer Inc.
Palbociclib (CAS 571190-30-2) is a selective inhibitor of cyclin-dependent kinases CDK4 and CDK6, which control cell cycle progression. Known in research as PF-00080665, this compound plays an important role in studies focused on cancer cell proliferation and targeted therapeutic strategies. The palbociclib cas number is widely referenced in biochemical databases, while identifiers such as 571190-30-2 cas and cas 571190-30-2 are commonly used in laboratory procurement and research documentation.
Researchers frequently investigate the palbociclib chemical structure to better understand its interaction with kinase domains responsible for regulating the cell cycle. The compound has a defined palbociclib molecular formula and stable physicochemical properties suitable for experimental use. Laboratories involved in oncology research often buy 571190-30-2 to study cell cycle regulation and to evaluate new approaches for inhibiting uncontrolled tumor cell proliferation.
Palbociclib is widely used in biomedical research investigating mechanisms of cell cycle control and cancer development. By selectively inhibiting CDK4 and CDK6, the compound allows researchers to study signaling pathways that regulate cell division and tumor growth.
In vitro studies show that Palbociclib effectively blocks CDK4/6 activity, preventing phosphorylation of the retinoblastoma protein (Rb) and thereby stopping cell cycle progression at the G1 phase. This inhibition reduces proliferation of cancer cell lines that rely on CDK4/6 signaling for growth, making Palbociclib a valuable reference compound for experimental oncology studies.
In vivo models have demonstrated that CDK4/6 inhibition can suppress tumor growth by limiting uncontrolled cell division. Studies involving PF-00080665 help researchers investigate how cell cycle inhibition influences tumor progression and therapeutic response in preclinical cancer models.
The biochemical activity of Palbociclib involves selective inhibition of cyclin-dependent kinases CDK4 and CDK6. By blocking phosphorylation events required for cell cycle progression, the compound interferes with molecular pathways responsible for uncontrolled cellular proliferation.
High-quality bioactive compounds enable researchers to explore molecular targets and signaling pathways with greater precision. Access to validated reference molecules supports drug discovery programs and helps scientists better understand mechanisms involved in cancer biology and targeted therapy development.
SDS
PBC | PD 0332991 | PD 332991 | PD-332991 | ibrance | palbociclib
The compound has purity validated by NMR and/or LCMS methods.
1 mg
$19
2 mg
$19
5 mg
$19
10 mg
$19
15 mg
$19
20 mg
$19
25 mg
$19
30 mg
$19
35 mg
$19
40 mg
$64
45 mg
$21
50 mg
$22
75 mg
$29
100 mg
$74
Quantity
1
Total amount
$ 19
PBC | PD 0332991 | PD 332991 | PD-332991 | ibrance | palbociclib
The compound has purity validated by NMR and/or LCMS methods.
Target activity features
It should be emphasized that the product may be active against a larger number of targets than shown on the card. The information represented here refers to the targets with the largest value of pX or the targets with ΔpX less than 1.5 from the largest pX value.