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AROMATASE INHIBITOR I-1MG - 182540-1MG, 1 mg

PROLYL ENDOPEPTIDASE INHIBITOR - 537011-5MG

VEGF INHIBITOR FLT2-11-1MG - 676493-1MG

VEGF INHIBITOR V1-1MG - 676495-1MG

BRYOSTATIN 1-10UG - 203811-10UG

BTS. 5mg. N-Benzyl-p-toluenesulphonamide. White powder. Protect from light. Packaged under inert gas. Potent inhibitor of Ca2+-stimulated myosin S1 ATPase & reversibly blocks the gliding motility. Weakens myosinGs interaction with F-actin. Purity=95% HPLC. CAS 1576-37-0. MW 261.3

CGP-37157. 5mg. 7-Chloro-5-(2-chlorophenyl)-1,5-dihydro-4,1-benzothiazepin-2(3H)-one. White solid. Cell-permeable benzothiazepine derivative of clonazepam acting as specific & potent inhibitor of mitochondrial Na+/Ca2+ exchanger. Purity:=98% by TLC. CAS 75450-34-9. MW 324.2.

ERK ACTIVATION INHIBITOR PEPTI - 328000-1MG

ERK ACTIVATION INHIBITOR PEPTI - 328005-1MG

GSK-3 beta Inhibitor I. 5mg. TDZD-8. 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione. Off-white solid. Packaged under inert gas. A thiadiazolidinone (TDZD) analog acting as highly selective, non-ATP competitive inhibitor of GSK-3b.Binds to active site of GSK-3b. Purity:=95% HPLC. MW 222.3.

IKB KINASE INHIBITOR PEPTIDE - 401477-1MG

IKB KINASE INACTIVE CONTROL PE - 401478-1MG

JAK3 INHIBITOR IV-10MG - 420121-10MG

JAK3 INHIBITOR V-10MG - 420122-10MG

NF 279-5MG - 480418-5MG

NNOS INHIBITOR I-5MG - 490070-5MG

Pravastatin, Sodium Salt. 25mg. 3 beta -Hydroxycompactin, Na. White solid. Water-soluble, competitive 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that potently blocks in vivo cholesterol synthesis. Purity: =98% by HPLC. CAS 81131-70-6. Hygroscopic. MW 446.5.

PRIMA-1. 10mg. 2,2-Bis(hydroxymethyl)-1-azabicyclo[2,2,2]octan-3-one. p53 Reactivation and Induction of Massive Apoptosis. Off-white solid. Hygroscopic. Packaged under inert gas. A cell-permeable quinuclidinone analog with antitumor properties. Purity: =95% by TLC. MW 185.2.

STAT3 Inhibitor Peptide, Cell-Permeable. 1mg. White lyophilized solid. A cell-permeable analog of the Stat3-SH2 domain-binding phosphopeptide that contains a C-terminal membrane translocating sequence and acts as a highly selective, potent blocker of Stat3 activation. Purity: =95% HPLC.

17-AAG-500UG - 100068-500UG

ADAAHX3L3VS-250UG - 114802-250UG

8-CPT-2'-O-ME-CAMP-5UMOL - 116833-5UMOL

AICA-RIBOSIDE-50MG - 123040-50MG

AKT INHIBITOR II-1MG - 124008-1MG

AKT INHIBITOR III-1MG - 124009-1MG

ALENDRONATE SODIUM SALT-100MG - 126855-100MG

ANTHRAX LETHAL FACTOR PROTEASE - 176901-1MG

APOPTOSIS INHIBITOR-10MG - 178488-10MG

BARK1 INHIBITOR-5MG - 182200-5MG

AUTOCAMTIDE-2 RELATED INHIBITO - 189485-1MG

5-AZA-2'-DEOXYCYTIDINE-25MG - 189825-25MG

CATHEPSIN G INHIBITOR I-1MG - 219372-1MG

CATHEPSIN K INHIBITOR I-5MG - 219377-5MG

CATHEPSIN K INHIBITOR II-1MG - 219379-1MG

CATHEPSIN K INHIBITOR III-1MG - 219381-1MG

CLODRONATE DISODIUM SALT-10MG - 233183-10MG

COX-2 INHIBITOR I-5MG - 236011-5MG

GGACK-5MG - 347436-5MG

GW1929-1MG - 370695-1MG

JAK INHIBITOR I-500UG - 420099-500UG

JNK INHIBITOR II NEGATIVE CON - 420123-1MG

MMP-9 INHIBITOR I-500UG - 444278-500UG

MK571 SODIUM SALT 5MG - 475874-5MG

MYOSIN LIGHT CHAIN KINASE INHI - 475981-5MG

OMEPRAZOLE-50MG - 496100-50MG

PEPSTATIN A METHYL ESTER-1MG - 516485-1MG

PROTEASE INHIBITOR COCKTAIL SE - 539133-1ML

PROTEASE INHIBITOR COCKTAIL SE - 539133-1SET

RO106-9920-1MG - 557550-1MG

SANT-1-5MG - 559303-5MG

SB-218078-1MG - 559402-1MG

SB 239063-500UG - 559404-500UG

G-SECRETASE INHIBITOR XVI-5MG - 565777-5MG

T0901317-10MG - 575310-10MG

TIRAP INHIBITOR PEPTIDE CELL- - 613570-1MG

TIRAP INHIBITOR PEPTIDE CONTR - 613571-1MG

RILUZOLE-50MG - 557324-50MG

WISKOSTATIN-5MG - 681525-5MG

RAC1 INHIBITOR 5MG - 553502-5MG, 5 mg

CDK1 INHIBITOR CGP74514A-5MG - 217696-5MG, 5 mg

FASCAPLYSIN SYNTHETIC 1MG - 341251-1MG

RATJADONE A SYNTHETIC-2UG - 553590-2UG, 2 µg

CFTR INHIBITOR-172-5MG - 219670-5MG

PKR INHIBITOR 10MG - 527455-10MG

(-)-BLEBBISTATIN-1MG - 203391-1MG

APOPTOSIS INHIBITOR II NS3694 - 178494-10MG, 10 mg

FAS/FASL ANTAGONIST KP7-6-25MG - 341291-25MG

GSK-3B Inhibitor VI. An irreversible, non-ATP competitive inhibitor of GSK-3B (IC50=1uM).

CDK4 INHIBITOR-1MG - 219476-1MG

Caspace-3/7 Inhibitor II. A potent, reversible active site binding inhibitor of caspases-3 and -7 (IC50=3.2nM and 22.6nM, repsectively).

DNA-PK INHIBITOR-10MG - 260960-10MG

APOPTOSIS ACTIVATOR III 10MG - 178493-10MG

UCH-L1 INHIBITOR-10MG - 662086-10MG

P38 MAP KINASE INHIBITOR III-1 - 506121-1MG

IKK INHIBITOR III BMS-345541- - 401480-1MG

PROTEIN SYNTHESIS INITIATION I - 539690-25MG

CDK2 INHIBITOR III-5MG - 238803-5MG

CDK2 INHIBITOR III-1MG - 238803-1MG

GSK-3BETA PEPTIDE INHIBITOR-1M - 361546-1MG

H-GLY-ARG-ALA-ASP-SER-PRO-OH-5 - 03-34-0052-5MG

OLOMOUCINE II-5MG - 495621-5MG

NFAT INHIBITOR 1MG - 480401-1MG

A1-PDX HUMAN RECOMBINANT 2.5MG - 126850-2.5MG

CASEIN KINASE I INHIBITOR 1MG - 218696-1MG

CALPAIN INHIBITOR XI-1MG - 208743-1MG

CALPAIN INHIBITOR XI-5MG - 208743-5MG

LIPOXIN A4 15-EPI-25UG - 437725-25UG

COX-1 INHIBITOR FR122047-5MG - 236005-5MG

FORMYL PEPTIDE RECEPTOR 5MG - 344216-5MG

BAX CHANNEL BLOCKER-5MG - 196805-5MG

JAK3 INHIBITOR VI-5MG - 420126-5MG

EB-47-1MG - 324473-1MG

TOFA-5MG - 613450-5MG

ELASTASE INHIBITOR IV 1MG - 324759-1MG

PROTEIN TYROSINE I 10MG - 540211-10MG

DNA-PK INHIBITOR II-5MG - 260961-5MG

JERVINE-1MG - 420210-1MG

TX-1918-10MG - 655203-10MG

GSK-3B INHIBITOR VII-5MG - 361548-5MG

WISKOSTATIN 1MG - 681525-1MG

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