CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 1 of 1
Non-Antibody Products
Page 1,068 of 1,297
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| (2R)-Octyl-α-hydroxyglutarate | A cell-permeable derivative of the D-isomer of 2-HG; used to examine the c… | 5 mg | 16366-5 | More Info |
| (2R)-Octyl-α-hydroxyglutarate-d17 | An internal standard for the quantification of (2R)-octyl-α-hydroxyg… | 1 mg | 19694-1 | More Info |
| (2R)-Octyl-α-hydroxyglutarate-d17 | An internal standard for the quantification of (2R)-octyl-α-hydroxyg… | 5 mg | 19694-5 | More Info |
| (2R)-Octyl-α-hydroxyglutarate-d17 | An internal standard for the quantification of (2R)-octyl-α-hydroxyg… | 500 µg | 19694-500 | More Info |
| Rocuronium (bromide) | A non-depolarizing muscle relaxant; selectively induces neuromuscular bloc… | 10 mg | 23698-10 | More Info |
| Rocuronium (bromide) | A non-depolarizing muscle relaxant; selectively induces neuromuscular bloc… | 25 mg | 23698-25 | More Info |
| Rocuronium (bromide) | A non-depolarizing muscle relaxant; selectively induces neuromuscular bloc… | 5 mg | 23698-5 | More Info |
| Rocuronium (bromide) | A non-depolarizing muscle relaxant; selectively induces neuromuscular bloc… | 50 mg | 23698-50 | More Info |
| Rofecoxib | A NSAID that selectively inhibits COX-2 over COX-1 (IC50s = 0.018 and >15… | 100 mg | 10010260-100 | More Info |
| Rofecoxib | A NSAID that selectively inhibits COX-2 over COX-1 (IC50s = 0.018 and >15… | 250 mg | 10010260-250 | More Info |
| Rofecoxib | A NSAID that selectively inhibits COX-2 over COX-1 (IC50s = 0.018 and >15… | 50 mg | 10010260-50 | More Info |
| Rofecoxib | A NSAID that selectively inhibits COX-2 over COX-1 (IC50s = 0.018 and >15… | 500 mg | 10010260-500 | More Info |
| Rofecoxib-d5 | An internal standard for the quantification of rofecoxib by GC- or LC-MS | 1 mg | 28900-1 | More Info |
| Rofecoxib-d5 | An internal standard for the quantification of rofecoxib by GC- or LC-MS | 500 µg | 28900-500 | More Info |
| (R)-Ofloxacin | A fluoroquinolone antibiotic; the (R) isomer of ofloxacin and levofloxacin… | 1 mg | 29601-1 | More Info |
| (R)-Ofloxacin | A fluoroquinolone antibiotic; the (R) isomer of ofloxacin and levofloxacin… | 10 mg | 29601-10 | More Info |
| (R)-Ofloxacin | A fluoroquinolone antibiotic; the (R) isomer of ofloxacin and levofloxacin… | 25 mg | 29601-25 | More Info |
| (R)-Ofloxacin | A fluoroquinolone antibiotic; the (R) isomer of ofloxacin and levofloxacin… | 5 mg | 29601-5 | More Info |
| Roflumilast | A PDE4 inhibitor (IC50 = 0.8 nM); selective for PDE4 over PDE1, -2, -3, an… | 1 mg | 15141-1 | More Info |
| Roflumilast | A PDE4 inhibitor (IC50 = 0.8 nM); selective for PDE4 over PDE1, -2, -3, an… | 10 mg | 15141-10 | More Info |
| Roflumilast | A PDE4 inhibitor (IC50 = 0.8 nM); selective for PDE4 over PDE1, -2, -3, an… | 25 mg | 15141-25 | More Info |
| Roflumilast | A PDE4 inhibitor (IC50 = 0.8 nM); selective for PDE4 over PDE1, -2, -3, an… | 5 mg | 15141-5 | More Info |
| Roflumilast-d4 | An internal standard for the quantification of roflumilast by GC- or LC-MS, | 1 mg | 18260-1 | More Info |
| Roflumilast-d4 | An internal standard for the quantification of roflumilast by GC- or LC-MS, | 500 µg | 18260-500 | More Info |
| Roflumilast N-oxide | A PDE4 inhibitor (IC50 = 2 nM) and active metabolite of roflumilast; selec… | 10 mg | 33975-10 | More Info |
| Roflumilast N-oxide | A PDE4 inhibitor (IC50 = 2 nM) and active metabolite of roflumilast; selec… | 25 mg | 33975-25 | More Info |
| Roflumilast N-oxide | A PDE4 inhibitor (IC50 = 2 nM) and active metabolite of roflumilast; selec… | 5 mg | 33975-5 | More Info |
| Ro 04-6790 (hydrochloride hydrate) | A 5-HT6 receptor antagonist (Ki = 44.7 nM); selective for 5-HT6 receptors… | 10 mg | 34476-10 | More Info |
| Ro 04-6790 (hydrochloride hydrate) | A 5-HT6 receptor antagonist (Ki = 44.7 nM); selective for 5-HT6 receptors… | 25 mg | 34476-25 | More Info |
| Ro 04-6790 (hydrochloride hydrate) | A 5-HT6 receptor antagonist (Ki = 44.7 nM); selective for 5-HT6 receptors… | 5 mg | 34476-5 | More Info |
| Rolapitant | A potent NK1 receptor antagonist (Ki = 0.66 nM for the human receptor); gr… | 1 mg | 23906-1 | More Info |
| Rolapitant | A potent NK1 receptor antagonist (Ki = 0.66 nM for the human receptor); gr… | 10 mg | 23906-10 | More Info |
| Rolapitant | A potent NK1 receptor antagonist (Ki = 0.66 nM for the human receptor); gr… | 5 mg | 23906-5 | More Info |
| Rolicyclidine (hydrochloride) | An arylcyclohexylamine that produces stimulant effects in rats similar to… | 1 mg | 19263-1 | More Info |
| Rolicyclidine (hydrochloride) | An arylcyclohexylamine that produces stimulant effects in rats similar to… | 5 mg | 19263-5 | More Info |
| Rolitetracycline | A tetracycline antibiotic; has bacteriostatic activity at low concentratio… | 25 mg | 23479-25 | More Info |
| Rolitetracycline | A tetracycline antibiotic; has bacteriostatic activity at low concentratio… | 5 mg | 23479-5 | More Info |
| Ro 25-6981 (maleate) | A potent, selective activity-dependent blocker of NMDA receptors containin… | 1 mg | 14578-1 | More Info |
| Ro 25-6981 (maleate) | A potent, selective activity-dependent blocker of NMDA receptors containin… | 10 mg | 14578-10 | More Info |
| Ro 25-6981 (maleate) | A potent, selective activity-dependent blocker of NMDA receptors containin… | 50 mg | 14578-50 | More Info |
| (R)-Omeprazole (sodium salt) | An inhibitor of the gastric H+/K+ ATPase and an enantiomer of esomeprazole… | 1 mg | 18874-1 | More Info |
| (R)-Omeprazole (sodium salt) | An inhibitor of the gastric H+/K+ ATPase and an enantiomer of esomeprazole… | 5 mg | 18874-5 | More Info |
| (R)-Omeprazole (sodium salt) | An inhibitor of the gastric H+/K+ ATPase and an enantiomer of esomeprazole… | 500 µg | 18874-500 | More Info |
| Romidepsin | A natural bicyclic depsipeptide that selectively inhibits class I HDACs (I… | 1 mg | 17130-1 | More Info |
| Romidepsin | A natural bicyclic depsipeptide that selectively inhibits class I HDACs (I… | 5 mg | 17130-5 | More Info |
| Romidepsin | A natural bicyclic depsipeptide that selectively inhibits class I HDACs (I… | 500 µg | 17130-500 | More Info |
| Romifidine (hydrochloride) | An analytical reference standard categorized as a sedative and analgesic;… | 1 mg | 38581-1 | More Info |
| Romifidine (hydrochloride) | An analytical reference standard categorized as a sedative and analgesic;… | 5 mg | 38581-5 | More Info |
| Romifidine (hydrochloride) | An α2-AR agonist; epidural administration induces antinociception an… | 10 mg | 36693-10 | More Info |
| Romifidine (hydrochloride) | An α2-AR agonist; epidural administration induces antinociception an… | 25 mg | 36693-25 | 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
Return to Profile