SF1126


Catalog No. Size PriceQuantity
M23846-C Contact sales@xcessbio.com for quotation $100Unavailable

Description

SF1126 is a relevant pan and dual first-in-class PI3K/BRD4 inhibitor, has antitumor and anti-angiogenic activity. SF1126 is an RGDS-conjugated LY294002 prodrug, which is designed to exhibit increased solubility and bind to specific integrins within the tumor compartment. SF1126 induces cell apoptosis.

Product information

CAS Number: 936487-67-1

Molecular Weight: 852.84

Formula: C39H48N8O14

Chemical Name: 4-{[(3-{[(1S)-1-[({[(1S)-2-carboxy-1-{[(1S)-1-carboxylato-2-hydroxyethyl]carbamoyl}ethyl]carbamoyl}methyl)carbamoyl]-4-[(diaminomethylidene)amino]butyl]carbamoyl}propanoyl)oxy]methyl}-4-(4-oxo-8-phenyl-4H-chromen-2-yl)morpholin-4-ium

Smiles: NC(N)=NCCC[C@H](NC(=O)CCC(=O)OC[N+]1(CCOCC1)C1=CC(=O)C2=CC=CC(=C2O1)C1C=CC=CC=1)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C([O-])=O

InChiKey: SVNJBEMPMKWDCO-KCHLEUMXSA-N

InChi: InChI=1S/C39H48N8O14/c40-39(41)42-13-5-10-26(36(55)43-20-31(51)45-27(18-33(52)53)37(56)46-28(21-48)38(57)58)44-30(50)11-12-34(54)60-22-47(14-16-59-17-15-47)32-19-29(49)25-9-4-8-24(35(25)61-32)23-6-2-1-3-7-23/h1-4,6-9,19,26-28,48H,5,10-18,20-22H2,(H9-,40,41,42,43,44,45,46,50,51,52,53,55,56,57,58)/t26-,27-,28-/m0/s1

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

SF1126 (0-6 µM; 48 hours) inhibits Hep3B, HepG2, SK-Hep1, and Huh7 cells proliferation with IC50s of 5.05, 6.89, 3.14, and 2.14 µM, respectively. SF1126 (1-10 µM; 24 hours) results in cell-cycle arrest with a proportional increase in G0-G1 and a decrease in the number of cells in the S-phase in Hep 3B, Hep G2, SK-Hep1, and Huh7 cells. SF1126 (0.5-2.5 µM; pre-30 minutes) and sorafenib suggests that combined treatment of SF1126 and sorafenib blocks multiple key enzymes in PI3K/AKT/mTOR and Ras/Raf/MAPK pathway.

Products are for research use only. Not for human use.

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