Cart
sales@molnova.com
PI3Kδ-IN-16
CAS No. 2766437-35-6
PI3Kδ-IN-16( —— )
Catalog No. M37034 CAS No. 2766437-35-6
PI3Kδ-IN-16 is a selective and potent PI3Kδ inhibitor with anticancer and antiproliferative activity, induces cell cycle arrest and apoptosis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 231 | Get Quote |
|
| 5MG | 359 | Get Quote |
|
| 10MG | 541 | Get Quote |
|
| 25MG | 821 | Get Quote |
|
| 50MG | 1122 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NamePI3Kδ-IN-16
-
NoteResearch use only, not for human use.
-
Brief DescriptionPI3Kδ-IN-16 is a selective and potent PI3Kδ inhibitor with anticancer and antiproliferative activity, induces cell cycle arrest and apoptosis.
-
DescriptionPI3Kδ-IN-16 is a potent and selective inhibitor of PI3Kδ. PI3Kδ-IN-16 has a strong anti-proliferative effect on cells, causing cell cycle arrest and inducing apoptosis.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayApoptosis
-
TargetApoptosis
-
RecptorApoptosis | PI3K
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2766437-35-6
-
Formula Weight406.48
-
Molecular FormulaC22H26N6O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESN([C@H](C(=O)N1CCN(C)CC1)C)C=2C3=C(C=CC(=C3)C=4C=CC(OC)=NC4)N=CN2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Lei H, et al. Discovery of potent and selective PI3Kδ inhibitors bearing amino acid fragments. Bioorg Chem. 2023 Sep;138:106594.?
molnova catalog
related products
-
Batabulin
Batabulin is an antitumor compound, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization.
-
Soyasapogenol B
Soyasapogenol B has anti-cancer, hypocholesterolemic, anticomplementary, hepatoprotective effects, it inhibits proliferation of cultured Hep-G2.
-
CMLD-2
CMLD-2 is an inhibitor of HuR-ARE interaction (Ki: 350 nM) that competitively binds HuR protein and disrupts its interaction with adenine element-rich (ARE) mRNA targets.
