MedKoo Biosciences, Inc.
About MedKoo Products
Careers at MedKoo
Browse all products
Browse products by research area
Newest stocked products
Process Research & Development
Antibody Drug Conjugation
Hapten Design and Synthesis
How To Order
Terms and Conditions
Download MedKoo Catalogues
Amino Acid Nomenclature Guide
Useful Free Databases
or product name starting with:
A 65186 is a Type A Cholecystokinin (CCK) receptor antagonist. Cholecystokinin (CC...
A 65281 is an antibacterial isothiazoloquinolone. It induces considerable DNA brea...
A 65282 is an antibacterial isothiazoloquinolone. It induces considerable DNA bre...
A 65317 is a selective renin inhibitor that causes a blockade of the renin-angiote...
A66 is a potent and highly selective p110α inhibitor with IC50 of 32 nM in a cell-...
A-674563 is a potent, orally available Akt1 inhibitor with an IC50 value of 11nM. ...
A6770 is an inhibitor of sphingosine-1-phosphate (S1P) lyase.
A 68552 is a cholecystokinin agonist.
A-687136 is an H3 antagonist which may play a role in cognition.
A-688057 is an H3 antagonist/inverse agonist that may play a role in cognition.
A 68828 is an atrial natriuretic factor analog. It improves renal function and red...
A 68930 is a dopamine D-1 receptor antagonist. It inhibits NLRP3 inflammasome acti...
A-68930 hydrochloride is a selective D1 dopamine receptor agonist.
A 69024 is a highly selective dopamine D-1 receptor antagonist. It is a radioligan...
A 69992 is an HIV anti-infective nucleoside. Its enantiomers (see Synonyms) also s...
A 70450 is an inhibitor of aspartyl proteinase. It can be used as an antifungal ag...
A 70874 has high potency and selectivity for cholecystokinin (CCK) A receptors.
A71378 is a Cholecystokinin (CCK) receptor agonist with high potency & selectivity...
A 71497 is the 3-formyl derivative of the antibiotic tosufloxacin. It produces hig...
A 71623 is a selective (Cholecystokinin) CCK-A agonist that suppresses food intakes.
A 71915 is an atrial natricuretic factor receptor antagonist. It blocks physiologi...
A 73209 is a nucleoside analog of the oxetanocin family. It originates from a clas...
A 740 is a biochemical.
A-740003 is a potent and selective P2X7 receptor antagonist. A-740003 has (IC(50)...
A 74273 is a nonpeptidic and renin inhibitor. It may be used to treat cardiovascul...
A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.
A 74932 is an inhibitor of DNA topoisomerases. It is a quinolone antibacterial age...
A 75925 is a nonnucleoside reverse transcriptase inhibitors (NNRTI). It works to i...
A 75925 has HIV antiviral & HIV type 1 protease inhibitory activity.
A-75943 is a bone resorption inhibitor from streptomyces.
A 75998 is an inhibitor of leuteinizing hormone-releasing hormone. It is a synth...
A 76154 is a novel octapeptide (leutenizing hormone releasing hormone) LHRH antago...
A 76889 is a HIV-1 protease inhibitor.
A-769662 is a potent, reversible AMP-activated protein kinase (AMPK) activator wit...
A 77003 is an antiretroviral agent and HIV-1 protease inhibitor. A77003 impairs HI...
A-770041 is a potent ans selective LCK inhibitor. Concanavalin A-stimulated IL-2 ...
A 77-01 is an inhibitor of TGF-β type I receptor superfamily activin-like kinase A...
A-77636 hydrochloride is a potent and selective dopamine D1-like receptor agonist.
A778317 is a novel, stereoselective, high-affinity antagonist.
A-779 is a peptide antagonist of the Mas receptor, also known as the angiotensin (...
A-784168 is a potent and selective antagonist of Vanilloid receptor type 1 (TRPV1).
A 78773 is a potent, selective, direct, and reversible 5-lipoxygenase inhibitor. I...
A 79175 is a 5-lipoxygenase inhibitor that increases bone formation. It may also h...
A-794278 is a bioactive chemical.
A-794282 is a selective mGluR1 antagonist.
A-796260 or A-796,260, also known as LTI-258, is a drug developed by Abbott Labora...
A 802715 is an anti-tumor agent that causes dose-dependent protection against lipo...
A-803467 is a potent and selective blocker of NaV1.8 channels (IC50 values are 8, ...
A-804598 is a P2X7 selective, competitive antagonist.
A 80556 is a fluoroquinolone antibiotic with potent antibacterial activity against...