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Casein Kinase CK2

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Casein Kinase CK2

Chemical Structure Cat. No. Product Name CAS No.
PF-5006739 Chemical Structure
BCP29752 PF-5006739 1293395-67-1
PF-5006739 is a potent casesin kinase 1δ/ε inhibitor (IC50 values are 3.9 and 17 nM, respectively). Mediates circadian rhythm phase-delaying effects in vivo. Attenuates opioid drug seeking behaviour in addiction in vivo models.
PF4800567 Chemical Structure
BCP28458 PF4800567 1188296-52-7
PF-4800567 is a selective inhibitor of casein kinase 1ε (CK1ε; IC50 = 32 nM) with greater than 20-fold selectivity over CK1δ.
TA-01 Chemical Structure
BCP24229 TA-01 1784751-18-3
TA-01 is a potent CK1 and p38 MAPK inhibitor, with IC50s of 6.4 nM, 6.8 nM, 6.7 nM for CK1ε, CK1δ and p38 MAPK, respectively.
Ellagic acid Chemical Structure
BCP10830 Ellagic acid 476-66-4
Ellagic acid is a polyphenolic antioxidant that is abundant in many fruits, vegetables, plant bark, and peels. It has anti-carcinogenic, anti-mutagenic, anti-inflammatory, and organ-preserving properties, presumably related to its ability to alter cytochrome P450 activity and improve metabolism and clearance of xenobiotics, as well as alter immune function.
IC 261 Chemical Structure
BCP16652 IC 261 186611-52-9
IC261 is a reversible, ATP-competitive inhibitor of casein kinase 1 (CK1) that inhibits Ckiδ and Ckiε (IC50 = ~1 μM for both), as well as CK1α (IC50 = 16 μM).
SR-3029 Chemical Structure
BCP20656 SR-3029 1454585-06-8
SR-3029 is a potent and selective casein kinase 1δ/1ε (CK1δ/ε) inhibitor with potent antiproliferative properties SR-3029 shoed IC50:= 97 nM in MTT assays against the human A375 melanoma cell line and have physical, in vitro and in vivo PK properties suitable for use in proof of principle animal xenograft studies against human cancer cell lines.
Emodin Chemical Structure
BCP18372 Emodin 518-82-1
Emodin is a naturally-occurring anthraquinone found in a variety of plants used in traditional Chinese medicine. Purified emodin has diverse effects, including the suppression of inflammation, dyslipidemia, and cancer.
D4476 Chemical Structure
BCP09776 D4476 301836-43-1
D4476, a cell-permeant inhibitor of CK1 (casein kinase 1), suppresses the site-specific phosphorylation and nuclear exclusion of FOXO1a.
LH846 Chemical Structure
BCP09669 LH846 639052-78-1
LH846 is a selective inhibitor of casein kinase (CK) 1δ (IC50 values are 290 nM, 1.3 uM and 2.5 uM for CK1δ, ε and α); displays no inhibitory activity at CK2.
PF670462 Chemical Structure
BCP04305 PF670462 950912-80-8
PF-670462, a selective CK1 ε/δ inhibitor, causes a significant phase delay in animal models of circadian rhythm; it remains unclear whether one of the kinases has a predominant role in regulating the circadian clock.
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