CDK8-IN-13
CAS No. 918523-75-8
CDK8-IN-13( —— )
Catalog No. M36400 CAS No. 918523-75-8
CDK8-IN-13 is a CDK8 inhibitor (IC50: 51.9 nM) with potent, selective and oral activity. CDK8-IN-13 induces apoptosis and reduces the expression of p-STAT1 S727 and p-STAT5 S726. CDK8-IN-13 exhibits anti-tumour activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 58 | Get Quote |
|
| 5MG | 90 | Get Quote |
|
| 10MG | 132 | Get Quote |
|
| 25MG | 214 | Get Quote |
|
| 50MG | 321 | Get Quote |
|
| 100MG | 464 | Get Quote |
|
| 500MG | 981 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameCDK8-IN-13
-
NoteResearch use only, not for human use.
-
Brief DescriptionCDK8-IN-13 is a CDK8 inhibitor (IC50: 51.9 nM) with potent, selective and oral activity. CDK8-IN-13 induces apoptosis and reduces the expression of p-STAT1 S727 and p-STAT5 S726. CDK8-IN-13 exhibits anti-tumour activity.
-
DescriptionCDK8-IN-13 is a potent, selective and orally active CDK8 inhibitor with an IC50 value of 51.9 nM. CDK8-IN-13 induces Apoptosis. CDK8-IN-13 decreases the expression of p-STAT1 S727 and p-STAT5 S726. CDK8-IN-13 shows antitumor activity.
-
In VitroCell Proliferation AssayCell Line:molm-13, HL-60, MV4-11, MGC-803, MDA-MB-231, A375, A549 cells Concentration:0-50 μM Incubation Time:Result:Showed antiproliferative activity with GC50s of 1.57, 1.00, 4.61, >50, >50, >50, >50 μM, respectively.Western Blot Analysis Cell Line:HCT-116 cells Concentration:1, 2.5, 5, 10 μM Incubation Time:12 h Result:Decreased the expression of p-STAT1 S727 and p-STAT5 S726, andsuppressed the phosphorylation of STAT1 S727 induced by IFN-γ (10 ng/mL) in a dose-dependent manner.Apoptosis Analysis Cell Line:HL-60 cells Concentration:0, 1, 5, 10 μM Incubation Time:48 h Result:Induced approximately 7% and 36% apoptotic at concentrations of 5 and 10 μM, respectively.
-
In VivoAnimal Model:6-week-old Balb/C mice (C1498 cells)Dosage:40, 80 mg/kg Administration:P.o.; for 15 days Result:Decreased the tumor growth with no significant weight loss,the expression of Ki67 decreased in a dose-dependent manner, the level of phosphorylation of STAT1 S727 in tumor tissues was downregulated.
-
Synonyms——
-
PathwayApoptosis
-
TargetApoptosis
-
RecptorApoptosis | CDK
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number918523-75-8
-
Formula Weight237.26
-
Molecular FormulaC14H11N3O
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 125 mg/mL (526.85 mM; Ultrasonic )
-
SMILESC(N)(=O)C=1C=C(C=2C=C3C(=NC2)NC=C3)C=CC1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Zhang XX, et al. Discovery of a novel oral type Ⅰ CDK8 inhibitor against acute myeloid leukemia. Eur J Med Chem. 2023 May 5;251:115214.?
molnova catalog
related products
-
(-)-Epipodophyllotox...
(-)-Epipodophyllotoxin (2) is an antiproliferative agent against cancer cells with GI50s of 0.36 and 0.24 μM in HeLa cells and MCF-7 cells, respectively. (-)-Epipodophyllotoxin can inhibit mitotic spindle assembly in vitro.
-
Tetrac
Tetrac (Tetraiodothyroacetic acid) is a derivative of L-thyroxine (T4), a thyroxine integrin receptor antagonist.Tetrac induces antiproliferation by blocking EGFR-mediated cell signaling in colorectal cancer cells.
-
icFSP1
icFSP1 is a mitochondria-associated apoptosis-inducing factor regulator with antitumor activity for the study and treatment of tumor diseases.
Cart
sales@molnova.com