CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 690 of 1
Non-Antibody Products
Page 690 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Lotusine | An alkaloid with diverse biological activities; increases cAMP levels in r… | 25 mg | 35136-25 | More Info |
| Lotusine | An alkaloid with diverse biological activities; increases cAMP levels in r… | 5 mg | 35136-5 | More Info |
| Lotusine | An alkaloid with diverse biological activities; increases cAMP levels in r… | 50 mg | 35136-50 | More Info |
| Loureirin B | A flavonoid with diverse biological activities; inhibits Kv1.3-mediated cu… | 1 mg | 27454-1 | More Info |
| Loureirin B | A flavonoid with diverse biological activities; inhibits Kv1.3-mediated cu… | 10 mg | 27454-10 | More Info |
| Loureirin B | A flavonoid with diverse biological activities; inhibits Kv1.3-mediated cu… | 25 mg | 27454-25 | More Info |
| Loureirin B | A flavonoid with diverse biological activities; inhibits Kv1.3-mediated cu… | 5 mg | 27454-5 | More Info |
| Lovastatin | An inhibitor of HMG-CoA reductase (Ki = 1.4 nM); a prodrug form of lovasta… | 10 mg | 10010338-10 | More Info |
| Lovastatin | An inhibitor of HMG-CoA reductase (Ki = 1.4 nM); a prodrug form of lovasta… | 5 mg | 10010338-5 | More Info |
| Lovastatin | An inhibitor of HMG-CoA reductase (Ki = 1.4 nM); a prodrug form of lovasta… | 50 mg | 10010338-50 | More Info |
| Lovastatin-d9 | An internal standard for the quantification of lovastatin by GC- or LC-MS | 1 mg | 26461-1 | More Info |
| Lovastatin Hydroxy Acid (sodium salt) | A potent and competitive HMG-CoA reductase inhibitor (Ki = 0.6 nM); is the… | 1 mg | 10010339-1 | More Info |
| Lovastatin Hydroxy Acid (sodium salt) | A potent and competitive HMG-CoA reductase inhibitor (Ki = 0.6 nM); is the… | 10 mg | 10010339-10 | More Info |
| Lovastatin Hydroxy Acid (sodium salt) | A potent and competitive HMG-CoA reductase inhibitor (Ki = 0.6 nM); is the… | 25 mg | 10010339-25 | More Info |
| Lovastatin Hydroxy Acid (sodium salt) | A potent and competitive HMG-CoA reductase inhibitor (Ki = 0.6 nM); is the… | 5 mg | 10010339-5 | More Info |
| Loxapine-d8 | An internal standard for the quantification of loxapine by GC- or LC-MS | 1 mg | 33537-1 | More Info |
| Loxapine-d8 | An internal standard for the quantification of loxapine by GC- or LC-MS | 5 mg | 33537-5 | More Info |
| Loxapine (succinate) | An atypical antipsychotic drug that displays high affinity for histamine (… | 100 mg | 20760-100 | More Info |
| Loxapine (succinate) | An atypical antipsychotic drug that displays high affinity for histamine (… | 50 mg | 20760-50 | More Info |
| Loxapine (succinate) | An atypical antipsychotic drug that displays high affinity for histamine (… | 500 mg | 20760-500 | More Info |
| Loxiglumide | A CCK receptor antagonist (Kis = 9.1 and 0.33 µM for CCK-8 binding t… | 10 mg | 25534-10 | More Info |
| Loxiglumide | A CCK receptor antagonist (Kis = 9.1 and 0.33 µM for CCK-8 binding t… | 25 mg | 25534-25 | More Info |
| Loxiglumide | A CCK receptor antagonist (Kis = 9.1 and 0.33 µM for CCK-8 binding t… | 5 mg | 25534-5 | More Info |
| Loxiglumide | A CCK receptor antagonist (Kis = 9.1 and 0.33 µM for CCK-8 binding t… | 50 mg | 25534-50 | More Info |
| LOXO-101 | A pan-Trk inhibitor (IC50s = 2-20 nM for TrkA, TrkB, and TrkC); selective… | 1 mg | 27056-1 | More Info |
| LOXO-101 | A pan-Trk inhibitor (IC50s = 2-20 nM for TrkA, TrkB, and TrkC); selective… | 10 mg | 27056-10 | More Info |
| LOXO-101 | A pan-Trk inhibitor (IC50s = 2-20 nM for TrkA, TrkB, and TrkC); selective… | 25 mg | 27056-25 | More Info |
| LOXO-101 | A pan-Trk inhibitor (IC50s = 2-20 nM for TrkA, TrkB, and TrkC); selective… | 5 mg | 27056-5 | More Info |
| LOXO-195 | An inhibitor of TrkA and TrkC (IC50s = 0.6 and G595R, TrkAG667C, TrkCG623R… | 1 mg | 27062-1 | More Info |
| LOXO-195 | An inhibitor of TrkA and TrkC (IC50s = 0.6 and G595R, TrkAG667C, TrkCG623R… | 10 mg | 27062-10 | More Info |
| LOXO-195 | An inhibitor of TrkA and TrkC (IC50s = 0.6 and G595R, TrkAG667C, TrkCG623R… | 5 mg | 27062-5 | More Info |
| LOXO-292 | A RET kinase inhibitor; inhibits phosphorylation of a KIF5B-RET fusion pro… | 10 mg | 33515-10 | More Info |
| LOXO-292 | A RET kinase inhibitor; inhibits phosphorylation of a KIF5B-RET fusion pro… | 25 mg | 33515-25 | More Info |
| LOXO-292 | A RET kinase inhibitor; inhibits phosphorylation of a KIF5B-RET fusion pro… | 5 mg | 33515-5 | More Info |
| LOXO-292 | A RET kinase inhibitor; inhibits phosphorylation of a KIF5B-RET fusion pro… | 50 mg | 33515-50 | More Info |
| Loxoprofen (sodium salt) | An NSAID and a prodrug form of loxoprofen-SRS; inhibits COX-1 and COX-2 in… | 1 g | 35088-1 | More Info |
| Loxoprofen (sodium salt) | An NSAID and a prodrug form of loxoprofen-SRS; inhibits COX-1 and COX-2 in… | 5 g | 35088-5 | More Info |
| Loxoprofen-SRS | An NSAID, a COX inhibitor (IC50s = 0.5 and 0.39 for recombinant human COX-… | 1 mg | 38122-1 | More Info |
| Loxoprofen-SRS | An NSAID, a COX inhibitor (IC50s = 0.5 and 0.39 for recombinant human COX-… | 10 mg | 38122-10 | More Info |
| Loxoprofen-SRS | An NSAID, a COX inhibitor (IC50s = 0.5 and 0.39 for recombinant human COX-… | 25 mg | 38122-25 | More Info |
| Loxoprofen-SRS | An NSAID, a COX inhibitor (IC50s = 0.5 and 0.39 for recombinant human COX-… | 5 mg | 38122-5 | More Info |
| Loxoribine | A guanosine derivative and an agonist of TLR7; selective for TLR7 over oth… | 10 mg | 21186-10 | More Info |
| Loxoribine | A guanosine derivative and an agonist of TLR7; selective for TLR7 over oth… | 25 mg | 21186-25 | More Info |
| Loxoribine | A guanosine derivative and an agonist of TLR7; selective for TLR7 over oth… | 5 mg | 21186-5 | More Info |
| Loxoribine | A guanosine derivative and an agonist of TLR7; selective for TLR7 over oth… | 50 mg | 21186-50 | More Info |
| LP-211 | An agonist of 5-HT7 receptors (Ki = 0.58 nM); selective for 5-HT7 over 5-H… | 10 mg | 29659-10 | More Info |
| LP-211 | An agonist of 5-HT7 receptors (Ki = 0.58 nM); selective for 5-HT7 over 5-H… | 25 mg | 29659-25 | More Info |
| LP-211 | An agonist of 5-HT7 receptors (Ki = 0.58 nM); selective for 5-HT7 over 5-H… | 5 mg | 29659-5 | More Info |
| LP-211 | An agonist of 5-HT7 receptors (Ki = 0.58 nM); selective for 5-HT7 over 5-H… | 50 mg | 29659-50 | More Info |
| LP-533401 | An inhibitor of Tph1 that blocks the biosynthesis of gut-derived serotonin… | 1 mg | 10492-1 | 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
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