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Amino Acid Nomenclature Guide
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NMR Chemical Shifts of Impurities Charts
MedKoo Chemical Nomenclature
or product name starting with:
A-484954 is an ATP-competitive inhibitor of eukaryotic elongation factor-2 kinase ...
A-485 is a potent and selective HAT inhibitor of p300/CBP in vitro with an IC50 of...
A 49816 is a high-ceiling diuretic.
A-49816 hydrochloride is a diuretic.
A51493A is a novel anthracyclinone antibiotic produced by a strain of Streptomyces...
A 53385 is a biochemical.
A 53693 is a selective adrenergic agonist with a chemical classification as a rigi...
A 53868A is an antibiotic isolated from Streptomyces luridus.
A-552 is a first-in-class potent antagonist of human IL-36γ, but not the closely r...
A 55453 is a radiated ionophore used as a high-affinity alpha 1-adrenergic recepto...
A 56234 is a high-ceiling diuretic.
A-57696 is a cholecystokinin antagonist. It is selective for cortical CCK-B recept...
A-582941 exhibits high-affinity binding and agonism at alpha-7 nicotinic acetylcho...
A-582941 is a positive allosteric modulator.
A 58365 A
A 58365 A is an angiotensin converting enzyme (ACE) inhibitor isolated from Strept...
A 58365 B
A 58365 B is an angiotensin converting enzyme (ACE) inhibitor isolated from Strept...
A 601 is a N-acylated serine-linked nonphosphorylated acylglucosamine-derived lipi...
A 60586 is a non-azole inhibitor of ergosterol biosynthesis. A60586 displays in-vi...
A61603 is an alpha-1A adrenergic receptor.
A61603 Hydrobromide is a selective alpha1A-adrenoceptor agonist.
A 62095 is a biochemical.
A 62176 is a potent topoisomerase inhibitor. It exhibits antineoplastic activity b...
A 62198 is a potent and selective renin inhibitor. A-62198 induced a dose-dependen...
A 63162 is a 5-lipoxygenase inhibitor.
A 643C is an investigative antidepressant.
A 64863 is a biochemical.
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)...