CDK
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<div class="colum_1 clearer"><p>CDKs (Cyclin-dependent kinases) are serine-threonine kinases first discovered for their role in regulating the cell cycle. They are also involved in regulating transcription, mRNA processing, and the differentiation of nerve cells. CDKs are relatively small proteins, with molecular weights ranging from 34 to 40 kDa, and contain little more than the kinase domain. In fact, yeast cells can proliferate normally when their CDK gene has been replaced with the homologous human gene. By definition, a CDK binds a regulatory protein called a cyclin. Without cyclin, CDK has little kinase activity; only the cyclin-CDK complex is an active kinase.</p><p>There are around 20 Cyclin-dependent kinases (CDK1-20) known till date. CDK1, 4 and 5 are involved in cell cycle, and CDK 7, 8, 9 and 11 are associated with transcription.</p><p>CDK levels remain relatively constant throughout the cell cycle and most regulation is post-translational. Most knowledge of CDK structure and function is based on CDKs of <i>S. pombe</i> (Cdc2), <i>S. cerevisia</i> (CDC28), and vertebrates (CDC2 and CDK2). The four major mechanisms of CDK regulation are cyclin binding, CAK phosphorylation, regulatory inhibitory phosphorylation, and binding of CDK inhibitory subunits (CKIs).</p></div>
Products Related to CDK(299)
- GC81522WWZ-11-098Purity: >98.00%
WWZ-11-098 is a selective CDK6 PROTAC degrader with DC 50 of 2.6 nM.
- GC81597Momilactone BCAS: 51415-08-8Purity: >99.00%
Momilactone B is an inhibitor of α-amylase and α-glucosidase, with an IC 50 of 146.85 μg/mL against Aspergillus oryzae α-amylase and an IC 50 of 612.03 μg/mL against Saccharomyces cerevisiae α-glucosidase.
- GC81862YJ1206 TFAPurity: >98.00%
YJ1206 TFA is an orally active selective CDK12 / CDK13 PROTAC degrader.
- GC81892Vevorisertib tetrahydrochloridePurity: >98.00%
Vevorisertib tetrahydrochloride (ARQ 751 tetrahydrochloride) is an orally active allosteric AKT inhibitor that blocks AKT phosphorylation.
- GF04054PROTAC CDK9 degrader-4CAS: 2411021-01-5Purity: >95.00%
PROTAC CDK9 degrader-4 is a PROTAC protein degrader that targets CDK9 (cyclin-dependent kinase 9).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC81453 | FOXM1-IN-3 | - | >98% | |
FOXM1-IN-3 is a potent FOXM1 inhibitor. | ||||
| GC81512 | dCDK9-202 | - | >98.50% | |
dCDK9-202 is a CDK9 PROTAC degrader with a DC 50 of 3.5 nM. | ||||
| GC81522 | WWZ-11-098 | - | >98.00% | |
WWZ-11-098 is a selective CDK6 PROTAC degrader with DC 50 of 2.6 nM. | ||||
| GC81597 | Momilactone B | 51415-08-8 | >99.00% | |
Momilactone B is an inhibitor of α-amylase and α-glucosidase, with an IC 50 of 146.85 μg/mL against Aspergillus oryzae α-amylase and an IC 50 of 612.03 μg/mL against Saccharomyces cerevisiae α-glucosidase. | ||||
| GC81862 | YJ1206 TFA | - | >98.00% | |
YJ1206 TFA is an orally active selective CDK12 / CDK13 PROTAC degrader. | ||||
| GC81892 | Vevorisertib tetrahydrochloride | - | >98.00% | |
Vevorisertib tetrahydrochloride (ARQ 751 tetrahydrochloride) is an orally active allosteric AKT inhibitor that blocks AKT phosphorylation. | ||||
| GC91419 | CYY292 | 2644673-04-9 | >98.00% | |
CYY292 is an inhibitor of PDGFRα, PDGFRβ, FGFR1, -2, and -3, (IC50s = 5.35, 4.6, 28, 28, and 78 nM, respectively). | ||||
| GF04054 | PROTAC CDK9 degrader-4 | 2411021-01-5 | >95.00% | |
PROTAC CDK9 degrader-4 is a PROTAC protein degrader that targets CDK9 (cyclin-dependent kinase 9). | ||||
| GN10017 | Wogonin | 632-85-9 | >98.00% | |
Wogonin is a potent and competitive inhibitor of CYP1A2 with a K i value of 0.24μM. | ||||
| GN10526 | Cucurbitacin E | 18444-66-1 | >99.50% | |
| GN10696 | Garcinone C | 76996-27-5 | >98% | |
