CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 691 of 1

Non-Antibody Products
Page 691 of 1,277
  • Records 34,501 - 34,550 of 63,825
Name Description Size Catalog #
Luteoloside A flavanoid with diverse biological activities; reduces LDH and caspase-3… 25 mg 25141-25 More Info
Luteoloside A flavanoid with diverse biological activities; reduces LDH and caspase-3… 5 mg 25141-5 More Info
Luteoloside A flavanoid with diverse biological activities; reduces LDH and caspase-3… 50 mg 25141-50 More Info
Luteoreticulin A nitro-containing bacterial metabolite; has mosquitocidal activity agains… 2.5 mg 25515-25 More Info
Luteoreticulin A nitro-containing bacterial metabolite; has mosquitocidal activity agains… 500 µg 25515-500 More Info
Luzindole A melatonin receptor antagonist that preferentially targets MT1B over MT1A… 10 mg 15998-10 More Info
Luzindole A melatonin receptor antagonist that preferentially targets MT1B over MT1A… 25 mg 15998-25 More Info
Luzindole A melatonin receptor antagonist that preferentially targets MT1B over MT1A… 5 mg 15998-5 More Info
Luzindole A melatonin receptor antagonist that preferentially targets MT1B over MT1A… 50 mg 15998-50 More Info
Luzopeptin A A cyclic depsipeptide antibiotic that displays antitumor activity; acts as… 1 mg 18444-1 More Info
L-Valacyclovir-d8 (hydrochloride) An internal standard for the quantification of valacyclovir by GC- or LC-MS 1 mg 31479-1 More Info
L-Valacyclovir-d8 (hydrochloride) An internal standard for the quantification of valacyclovir by GC- or LC-MS 500 µg 31479-500 More Info
L-Valacyclovir (hydrochloride) A prodrug of acyclovir; inhibits HSV-I replication (IC50 = 0.84 µM);… 100 mg 23801-100 More Info
L-Valacyclovir (hydrochloride) A prodrug of acyclovir; inhibits HSV-I replication (IC50 = 0.84 µM);… 25 mg 23801-25 More Info
L-Valacyclovir (hydrochloride) A prodrug of acyclovir; inhibits HSV-I replication (IC50 = 0.84 µM);… 250 mg 23801-250 More Info
L-Valacyclovir (hydrochloride) A prodrug of acyclovir; inhibits HSV-I replication (IC50 = 0.84 µM);… 50 mg 23801-50 More Info
L-Valine An essential amino acid; considered glucogenic due to its catabolism that… 100 g 38709-100 More Info
L-Valine An essential amino acid; considered glucogenic due to its catabolism that… 250 g 38709-250 More Info
L-Valine An essential amino acid; considered glucogenic due to its catabolism that… 500 g 38709-500 More Info
L-Valine-d8 An internal standard for the quantification of L-valine by GC- or LC-MS 1 mg 34830-1 More Info
L-Valine-d8 An internal standard for the quantification of L-valine by GC- or LC-MS 10 mg 34830-10 More Info
L-Valine-d8 An internal standard for the quantification of L-valine by GC- or LC-MS 25 mg 34830-25 More Info
L-Valine-d8 An internal standard for the quantification of L-valine by GC- or LC-MS 5 mg 34830-5 More Info
LX2343 An inhibitor of BACE1 and PI3K (IC50s = 11.43 and 15.99 µM, respecti… 1 mg 27799-1 More Info
LX2343 An inhibitor of BACE1 and PI3K (IC50s = 11.43 and 15.99 µM, respecti… 10 mg 27799-10 More Info
LX2343 An inhibitor of BACE1 and PI3K (IC50s = 11.43 and 15.99 µM, respecti… 5 mg 27799-5 More Info
LXH254 A pan-RAF inhibitor; selectively inhibits B-RAF and C-RAF over a panel of… 1 mg 28231-1 More Info
LXH254 A pan-RAF inhibitor; selectively inhibits B-RAF and C-RAF over a panel of… 10 mg 28231-10 More Info
LXH254 A pan-RAF inhibitor; selectively inhibits B-RAF and C-RAF over a panel of… 25 mg 28231-25 More Info
LXH254 A pan-RAF inhibitor; selectively inhibits B-RAF and C-RAF over a panel of… 5 mg 28231-5 More Info
LX7101 (hydrochloride) A potent inhibitor of LIMK1, LIMK2, ROCK1, and ROCK2 kinases (IC50s = 32,… 1 mg 21209-1 More Info
LX7101 (hydrochloride) A potent inhibitor of LIMK1, LIMK2, ROCK1, and ROCK2 kinases (IC50s = 32,… 10 mg 21209-10 More Info
LX7101 (hydrochloride) A potent inhibitor of LIMK1, LIMK2, ROCK1, and ROCK2 kinases (IC50s = 32,… 5 mg 21209-5 More Info
LXR-623 An LXR modulator that acts as a partial agonist at LXRα and a full a… 1 mg 21117-1 More Info
LXR-623 An LXR modulator that acts as a partial agonist at LXRα and a full a… 10 mg 21117-10 More Info
LXR-623 An LXR modulator that acts as a partial agonist at LXRα and a full a… 5 mg 21117-5 More Info
LXS-196 A PKC inhibitor (IC50s = 1.9 and 0.4 nM for PKCα and PKCθ, res… 1 mg 31455-1 More Info
LXS-196 A PKC inhibitor (IC50s = 1.9 and 0.4 nM for PKCα and PKCθ, res… 10 mg 31455-10 More Info
LXS-196 A PKC inhibitor (IC50s = 1.9 and 0.4 nM for PKCα and PKCθ, res… 25 mg 31455-25 More Info
LXS-196 A PKC inhibitor (IC50s = 1.9 and 0.4 nM for PKCα and PKCθ, res… 5 mg 31455-5 More Info
LY171883 Potent, orally active CysLT receptor antagonist with KB values of 0.07 and… 10 mg 70710-10 More Info
LY171883 Potent, orally active CysLT receptor antagonist with KB values of 0.07 and… 100 mg 70710-100 More Info
LY171883 Potent, orally active CysLT receptor antagonist with KB values of 0.07 and… 5 mg 70710-5 More Info
LY171883 Potent, orally active CysLT receptor antagonist with KB values of 0.07 and… 50 mg 70710-50 More Info
LY2090314 A potent and selective inhibitor of GSK3 (IC50s = 1.5 and 0.9 for human re… 1 mg 22211-1 More Info
LY2090314 A potent and selective inhibitor of GSK3 (IC50s = 1.5 and 0.9 for human re… 10 mg 22211-10 More Info
LY2090314 A potent and selective inhibitor of GSK3 (IC50s = 1.5 and 0.9 for human re… 25 mg 22211-25 More Info
LY2090314 A potent and selective inhibitor of GSK3 (IC50s = 1.5 and 0.9 for human re… 5 mg 22211-5 More Info
LY2109761 A small molecule inhibitor of the TGF-β receptor type 1 / type II kin… 1 mg 15409-1 More Info
LY2109761 A small molecule inhibitor of the TGF-β receptor type 1 / type II kin… 10 mg 15409-10 More Info
CAYMAN CHEMICAL COMPANY
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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