CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 826 of 1
Non-Antibody Products
Page 826 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| N-hydroxy MDA (hydrochloride) | An analog of MDA which inhibits reuptake of noradrenaline (IC50 = 87.8 &mi… | 50 mg | 13958-50 | More Info |
| N-hydroxy MDA (hydrochloride) (exempt preparation) | An analog of MDA which inhibits reuptake of noradrenaline (IC50 = 87.8 &mi… | 1 mg | 15688-1 | More Info |
| N-hydroxy MDMA (hemioxalate) | An analytical reference standard categorized as an amphetamine; intended f… | 1 mg | 9002345-1 | More Info |
| N-hydroxy MDMA (hemioxalate) | An analytical reference standard categorized as an amphetamine; intended f… | 5 mg | 9002345-5 | More Info |
| N-3-hydroxyoctanoyl-L-Homoserine lactone | A small diffusible signaling molecule secreted by various bacteria; can ha… | 1 mg | 9001150-1 | More Info |
| N-3-hydroxyoctanoyl-L-Homoserine lactone | A small diffusible signaling molecule secreted by various bacteria; can ha… | 10 mg | 9001150-10 | More Info |
| N-3-hydroxyoctanoyl-L-Homoserine lactone | A small diffusible signaling molecule secreted by various bacteria; can ha… | 25 mg | 9001150-25 | More Info |
| N-3-hydroxyoctanoyl-L-Homoserine lactone | A small diffusible signaling molecule secreted by various bacteria; can ha… | 5 mg | 9001150-5 | More Info |
| N-(3-hydroxyphenyl)-Arachidonoyl amide | An irreversible COX-2 inhibitor (IC50 = 2 µM) | 10 mg | 10007704-10 | More Info |
| N-(3-hydroxyphenyl)-Arachidonoyl amide | An irreversible COX-2 inhibitor (IC50 = 2 µM) | 100 mg | 10007704-100 | More Info |
| N-(3-hydroxyphenyl)-Arachidonoyl amide | An irreversible COX-2 inhibitor (IC50 = 2 µM) | 5 mg | 10007704-5 | More Info |
| N-(3-hydroxyphenyl)-Arachidonoyl amide | An irreversible COX-2 inhibitor (IC50 = 2 µM) | 50 mg | 10007704-50 | More Info |
| N-hydroxy Riluzole | A metabolite of riluzole | 1 mg | 33999-1 | More Info |
| N-hydroxy Riluzole | A metabolite of riluzole | 5 mg | 33999-5 | More Info |
| N-Hydroxysulfosuccinimide (sodium salt) | A modifying reagent that, in the presence of a cross-linking reagent, conv… | 1 g | 20680-1 | More Info |
| N-Hydroxysulfosuccinimide (sodium salt) | A modifying reagent that, in the presence of a cross-linking reagent, conv… | 250 mg | 20680-250 | More Info |
| N-Hydroxysulfosuccinimide (sodium salt) | A modifying reagent that, in the presence of a cross-linking reagent, conv… | 5 g | 20680-5 | More Info |
| N-Hydroxysulfosuccinimide (sodium salt) | A modifying reagent that, in the presence of a cross-linking reagent, conv… | 500 mg | 20680-500 | More Info |
| NI-42 | An inhibitor of the BRPF1 bromodomain (IC50 = 7.9 nM); selective for BRPF1… | 1 mg | 28293-1 | More Info |
| NI-42 | An inhibitor of the BRPF1 bromodomain (IC50 = 7.9 nM); selective for BRPF1… | 10 mg | 28293-10 | More Info |
| NI-42 | An inhibitor of the BRPF1 bromodomain (IC50 = 7.9 nM); selective for BRPF1… | 25 mg | 28293-25 | More Info |
| NI-42 | An inhibitor of the BRPF1 bromodomain (IC50 = 7.9 nM); selective for BRPF1… | 5 mg | 28293-5 | More Info |
| NI-57 | A selective, potent inhibitor of the bromodomains of BRPF proteins that bi… | 1 mg | 17662-1 | More Info |
| NI-57 | A selective, potent inhibitor of the bromodomains of BRPF proteins that bi… | 10 mg | 17662-10 | More Info |
| NI-57 | A selective, potent inhibitor of the bromodomains of BRPF proteins that bi… | 5 mg | 17662-5 | More Info |
| NI-57 | A selective, potent inhibitor of the bromodomains of BRPF proteins that bi… | 50 mg | 17662-50 | More Info |
| NIAD-4 | A fluorescent probe that crosses the blood-brain barrier; binds with high… | 1 mg | 18520-1 | More Info |
| NIAD-4 | A fluorescent probe that crosses the blood-brain barrier; binds with high… | 10 mg | 18520-10 | More Info |
| NIAD-4 | A fluorescent probe that crosses the blood-brain barrier; binds with high… | 5 mg | 18520-5 | More Info |
| NIBR0213 | A potent and selective S1P1 antagonist (IC50s = 2.5 and 2.0 nM for hS1P1 C… | 1 mg | 21513-1 | More Info |
| NIBR0213 | A potent and selective S1P1 antagonist (IC50s = 2.5 and 2.0 nM for hS1P1 C… | 10 mg | 21513-10 | More Info |
| NIBR0213 | A potent and selective S1P1 antagonist (IC50s = 2.5 and 2.0 nM for hS1P1 C… | 25 mg | 21513-25 | More Info |
| NIBR0213 | A potent and selective S1P1 antagonist (IC50s = 2.5 and 2.0 nM for hS1P1 C… | 5 mg | 21513-5 | More Info |
| NIBR17 | A PI3Kα inhibitor (IC50 = 50s = 0.09 and 0.73 µM, respectively… | 1 mg | 37312-1 | More Info |
| NIBR17 | A PI3Kα inhibitor (IC50 = 50s = 0.09 and 0.73 µM, respectively… | 10 mg | 37312-10 | More Info |
| NIBR17 | A PI3Kα inhibitor (IC50 = 50s = 0.09 and 0.73 µM, respectively… | 5 mg | 37312-5 | More Info |
| NIBR17 | A PI3Kα inhibitor (IC50 = 50s = 0.09 and 0.73 µM, respectively… | 50 mg | 37312-50 | More Info |
| NIBR189 | A selective antagonist of EBI2 (IC50s = 11 and 15 nM for human and mouse r… | 1 mg | 18792-1 | More Info |
| NIBR189 | A selective antagonist of EBI2 (IC50s = 11 and 15 nM for human and mouse r… | 10 mg | 18792-10 | More Info |
| NIBR189 | A selective antagonist of EBI2 (IC50s = 11 and 15 nM for human and mouse r… | 5 mg | 18792-5 | More Info |
| Nicaraven | An antioxidant; exhibits hydroxyl radical scavenging activity in vitro; re… | 10 mg | 23482-10 | More Info |
| Nicaraven | An antioxidant; exhibits hydroxyl radical scavenging activity in vitro; re… | 25 mg | 23482-25 | More Info |
| Nicaraven | An antioxidant; exhibits hydroxyl radical scavenging activity in vitro; re… | 5 mg | 23482-5 | More Info |
| Nicarbazine | A coccidiostat; prevents mortality of, and suppresses oocyst production in… | 100 g | 35110-100 | More Info |
| Nicarbazine | A coccidiostat; prevents mortality of, and suppresses oocyst production in… | 50 g | 35110-50 | More Info |
| Nicardipine (hydrochloride) | A dihydropyridine L-type calcium channel antagonist that displays antihype… | 1 g | 17537-1 | More Info |
| Nicardipine (hydrochloride) | A dihydropyridine L-type calcium channel antagonist that displays antihype… | 10 g | 17537-10 | More Info |
| Nicardipine (hydrochloride) | A dihydropyridine L-type calcium channel antagonist that displays antihype… | 25 g | 17537-25 | More Info |
| Nicardipine (hydrochloride) | A dihydropyridine L-type calcium channel antagonist that displays antihype… | 5 g | 17537-5 | More Info |
| Nicergoline | An α1-AR antagonist; binds to α1-ARs in rat brain membranes (K… | 1 g | 31573-1 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
Sales: sales@caymanchem.com
http://www.caymanchem.com
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