All ProductsDisplaying Products by Catalog Number (5500 - 5599)
0100020003000400050006000700080009001000110012001300140015001600170018001900200021002200230024002500260027002800290030003100320033003400350036003700380039004000410042004300440045004600470048004900500051005200530054005500560057005800590060006100620063006400650066006700680069007000710072007300740075007600770078007900800081008200830084008500860087008800
Cat. No. | Product Name / Activity |
---|---|
5500 | Protease Inhibitor Cocktail I |
Protease inhibitor cocktail for mammalian cells | |
5502 | Blasticidin S HCl |
Antibiotic; selection reagent for bis, bsr and BSD transformed cells | |
5506 | Vancomycin HCl |
Antibiotic | |
5509 | IPTG |
Used in cloning procedures with X-GAL | |
5512 | BIX NHE1 inhibitor |
Potent and selective NHE1 inhibitor | |
5515 | NADPH reduced form tetrasodium salt |
Cofactor for many anabolic enzymes | |
5517 | AMG PERK 44 |
Potent and selective PERK inhibitor; orally bioavailable | |
5520 | Echinomycin |
Highly potent and selective HIF-1α inhibitor | |
5521 | CIM 0216 |
Selective TRPM3 agonist | |
5522 | Napabucasin |
STAT3 inhibitor; also blocks cancer stem cell self-renewal | |
5523 | TAPI 0 |
ADAM-17 (TACE) and MMP inhibitor | |
5545 | BX 430 |
Selective P2X4 allosteric antagonist | |
5546 | NI 57 |
Potent and selective BRPF bromodomain inhibitor | |
5547 | MK6-83 |
TRPML channel activator | |
5548 | DREADD agonist 21 |
Potent hM3Dq and hM4Di DREADD agonist; blood brain barrier penetrant | |
5549 | Perlapine |
Potent hM3Dq and hM4Di DREADD agonist in vitro | |
5550 | E 2012 |
γ-secretase modulator; Notch-sparing | |
5553 | Sephin 1 |
Inhibitor of the regulatory subunit PPP1R15A of protein phosphatase 1 | |
5554 | IHR 1 |
Potent Smo antagonist | |
5559 | SSR 180711 hydrochloride |
Selective α7 nAChR partial agonist | |
5563 | VTP 27999 trifluoroacetate |
Highly potent and selective renin inhibitor | |
5564 | PBS, 100 Tablets |
PBS Tablets | |
5565 | Tiplaxtinin |
Plasminogen activator inhibitor-1 (PAI-1) inhibitor | |
5567 | EPZ 004777 |
Highly potent DOT1L inhibitor | |
5568 | S 18886 |
Potent thromboxane A2 (TP) antagonist | |
5570 | STOCK2S 26016 |
Lysine deficient protein kinase (WNK) signaling inhibitor | |
5577 | S4 |
High affinity and selective CA IX and CA XII inhibitor | |
5579 | Tilfrinib |
Potent and selective breast tumor kinase (Brk) inhibitor | |
5580 | DMH2 |
Type I BMP receptor inhibitor | |
5582 | TAT-cyclo-CLLFVY |
Selective HIF-1 dimerization inhibitor | |
5583 | Quin C1 |
Potent and selective FPR2 agonist | |
5584 | Aripiprazole |
High affinity D2 and 5-HT1A receptor partial agonist; also 5-HT2A antagonist | |
5585 | Balicatib |
Potent and selective cathepsin K inhibitor | |
5586 | Yoda 1 |
Piezo1 channel activator | |
5589 | WAY 181187 oxalate |
High affinity and selective 5-HT6 agonist | |
5590 | BI 9564 |
Potent and selective BRD9 and BRD7 inhibitor; orally active | |
5591 | I-BRD9 |
Potent and selective BRD9 inhibitor | |
5592 | LCB 03-0110 dihydrochloride |
Potent c-SRC kinase inhibitor; also inhibits DDR2, BTK and Syk | |
5594 | Spadin |
Potent K2P2.1 (TREK-1) channel blocker | |
5595 | A66 |
Potent and selective PI 3-kinase p110α inhibitor |