CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 691 of 859

Non-Antibody Products
Page 691 of 859
  • Records 51,751 - 51,825 of 64,374
Name Description Size Catalog #
Rat Peroxisome Proliferator-Activated Receptor Alpha Reporter Assay System rPPARα Reporter Cells are prepared using INDIGO's proprietary CryoMi… 3x32 Well 15764-332 More Info
Rat Peroxisome Proliferator-Activated Receptor Alpha Reporter Assay System rPPARα Reporter Cells are prepared using INDIGO's proprietary CryoMi… 96 Well 15764-96 More Info
Rat Peroxisome Proliferator-Activated Receptor Delta Assay System rPPARδ Reporter Cells are prepared using INDIGO's proprietary CryoMi… 3x32 Well 15765-332 More Info
Rat Peroxisome Proliferator-Activated Receptor Delta Assay System rPPARδ Reporter Cells are prepared using INDIGO's proprietary CryoMi… 96 Well 15765-96 More Info
Rat Pregnane X Receptor Reporter Assay System rPXR Reporter Cells are prepared using INDIGO's proprietary CryoMite&trade… 3x32 Well 17585-332 More Info
Rat Pregnane X Receptor Reporter Assay System rPXR Reporter Cells are prepared using INDIGO's proprietary CryoMite&trade… 96 Well 17585-96 More Info
Rat Progesterone Receptor Reporter Assay System Rat PGR Reporter Cells are prepared using INDIGO's proprietary CryoMite&tr… 3x32 Well 32581-332 More Info
Rat Progesterone Receptor Reporter Assay System Rat PGR Reporter Cells are prepared using INDIGO's proprietary CryoMite&tr… 96 Well 32581-96 More Info
Rat RAR-related Orphan Receptor Gamma Reporter Assay System rRORγ Reporter Cells are prepared using INDIGO's proprietary CryoMit… 3x32 Well 36154-332 More Info
Rat RAR-related Orphan Receptor Gamma Reporter Assay System rRORγ Reporter Cells are prepared using INDIGO's proprietary CryoMit… 96 Well 36154-96 More Info
Rauwolscine (hydrochloride) A natural alkaloid that acts as a selective and reversible α2-adrene… 100 mg 15596-100 More Info
Rauwolscine (hydrochloride) A natural alkaloid that acts as a selective and reversible α2-adrene… 250 mg 15596-250 More Info
Rauwolscine (hydrochloride) A natural alkaloid that acts as a selective and reversible α2-adrene… 50 mg 15596-50 More Info
Ravidasvir (hydrochloride) An NS5A inhibitor; inhibits HCV replication in Huh7 replicon cells contain… 1 mg 37794-1 More Info
Ravidasvir (hydrochloride) An NS5A inhibitor; inhibits HCV replication in Huh7 replicon cells contain… 10 mg 37794-10 More Info
Ravidasvir (hydrochloride) An NS5A inhibitor; inhibits HCV replication in Huh7 replicon cells contain… 25 mg 37794-25 More Info
Ravidasvir (hydrochloride) An NS5A inhibitor; inhibits HCV replication in Huh7 replicon cells contain… 5 mg 37794-5 More Info
Ravuconazole An orally available azole fungicide that potently inhibits the growth of a… 1 mg 18750-1 More Info
Ravuconazole An orally available azole fungicide that potently inhibits the growth of a… 10 mg 18750-10 More Info
Ravuconazole An orally available azole fungicide that potently inhibits the growth of a… 25 mg 18750-25 More Info
Ravuconazole An orally available azole fungicide that potently inhibits the growth of a… 5 mg 18750-5 More Info
Raxatrigine (hydrochloride) An inhibitor of voltage-gated sodium channels (IC50s = 22, 13, 23, 10, 84,… 1 mg 23490-1 More Info
Raxatrigine (hydrochloride) An inhibitor of voltage-gated sodium channels (IC50s = 22, 13, 23, 10, 84,… 10 mg 23490-10 More Info
Raxatrigine (hydrochloride) An inhibitor of voltage-gated sodium channels (IC50s = 22, 13, 23, 10, 84,… 25 mg 23490-25 More Info
Raxatrigine (hydrochloride) An inhibitor of voltage-gated sodium channels (IC50s = 22, 13, 23, 10, 84,… 5 mg 23490-5 More Info
RB394 An orally bioavailable inhibitor of sEH (IC50 = 0.33 µM) and agonist… 1 mg 18909-1 More Info
RB394 An orally bioavailable inhibitor of sEH (IC50 = 0.33 µM) and agonist… 10 mg 18909-10 More Info
RB394 An orally bioavailable inhibitor of sEH (IC50 = 0.33 µM) and agonist… 25 mg 18909-25 More Info
RB394 An orally bioavailable inhibitor of sEH (IC50 = 0.33 µM) and agonist… 5 mg 18909-5 More Info
(R)-BAY-598 An inhibitor of SMYD2 (IC50 = 1.7 µM); selective for SMYD2 over PAR1… 1 mg 29174-1 More Info
(R)-BAY-598 An inhibitor of SMYD2 (IC50 = 1.7 µM); selective for SMYD2 over PAR1… 10 mg 29174-10 More Info
(R)-BAY-598 An inhibitor of SMYD2 (IC50 = 1.7 µM); selective for SMYD2 over PAR1… 5 mg 29174-5 More Info
(R)-BAY-598 An inhibitor of SMYD2 (IC50 = 1.7 µM); selective for SMYD2 over PAR1… 500 µg 29174-500 More Info
(R)-(+)-BAY-K-8644 An L-type channel blocker that has negative inotropic and vasodilatory eff… 1 mg 15263-1 More Info
(R)-(+)-BAY-K-8644 An L-type channel blocker that has negative inotropic and vasodilatory eff… 10 mg 15263-10 More Info
(R)-(+)-BAY-K-8644 An L-type channel blocker that has negative inotropic and vasodilatory eff… 5 mg 15263-5 More Info
RbBP5 (human, recombinant) Source: Recombinant protein expressed in E. coli • AA: 2-538 (full le… 50 µg 10947-50 More Info
RBC8 An inhibitor of the Ras-like GTPases RalA and RalB; prevents spreading of… 1 mg 21281-1 More Info
RBC8 An inhibitor of the Ras-like GTPases RalA and RalB; prevents spreading of… 10 mg 21281-10 More Info
RBC8 An inhibitor of the Ras-like GTPases RalA and RalB; prevents spreading of… 25 mg 21281-25 More Info
RBC8 An inhibitor of the Ras-like GTPases RalA and RalB; prevents spreading of… 5 mg 21281-5 More Info
(R)-benzyl Mandelate A synthetic intermediate useful for pharmaceutical synthesis. 1 g 10007145-1 More Info
(R)-benzyl Mandelate A synthetic intermediate useful for pharmaceutical synthesis. 10 g 10007145-10 More Info
(R)-benzyl Mandelate A synthetic intermediate useful for pharmaceutical synthesis. 5 g 10007145-5 More Info
(R)-benzyl Mandelate A synthetic intermediate useful for pharmaceutical synthesis. 50 g 10007145-50 More Info
RBI 257 (maleate) A potent dopamine D4 receptor antagonist (Ki = 0.3 nM) that is selective o… 1 mg 17223-1 More Info
RBI 257 (maleate) A potent dopamine D4 receptor antagonist (Ki = 0.3 nM) that is selective o… 10 mg 17223-10 More Info
RBI 257 (maleate) A potent dopamine D4 receptor antagonist (Ki = 0.3 nM) that is selective o… 5 mg 17223-5 More Info
Rbin-1 An inhibitor of midasin; inhibits the growth of fission yeast strains in v… 1 mg 20745-1 More Info
Rbin-1 An inhibitor of midasin; inhibits the growth of fission yeast strains in v… 5 mg 20745-5 More Info
RBN-012759 A PARP14 inhibitor (IC50 = 0.003 µM); selective for PARP14 over PARP… 1 mg 36137-1 More Info
RBN-012759 A PARP14 inhibitor (IC50 = 0.003 µM); selective for PARP14 over PARP… 10 mg 36137-10 More Info
RBN-012759 A PARP14 inhibitor (IC50 = 0.003 µM); selective for PARP14 over PARP… 25 mg 36137-25 More Info
RBN-012759 A PARP14 inhibitor (IC50 = 0.003 µM); selective for PARP14 over PARP… 5 mg 36137-5 More Info
RBN-2397 A PARP7 inhibitor; stabilizes wild-type PARP7 levels, but not levels of th… 1 mg 33558-1 More Info
RBN-2397 A PARP7 inhibitor; stabilizes wild-type PARP7 levels, but not levels of th… 10 mg 33558-10 More Info
RBN-2397 A PARP7 inhibitor; stabilizes wild-type PARP7 levels, but not levels of th… 5 mg 33558-5 More Info
(R)-Bromoenol lactone A selective iPLA2γ inhibitor (IC50 = ~0.6 µM); selective for i… 1 mg 10006800-1 More Info
(R)-Bromoenol lactone A selective iPLA2γ inhibitor (IC50 = ~0.6 µM); selective for i… 10 mg 10006800-10 More Info
(R)-Bromoenol lactone A selective iPLA2γ inhibitor (IC50 = ~0.6 µM); selective for i… 5 mg 10006800-5 More Info
(R)-Bromoenol lactone A selective iPLA2γ inhibitor (IC50 = ~0.6 µM); selective for i… 500 µg 10006800-500 More Info
(R)-Bromoenol lactone-d7 An internal standard for the quantification of (R)-BEL by GC- or LC-MS 1 mg 10534-1 More Info
(R)-Bromoenol lactone-d7 An internal standard for the quantification of (R)-BEL by GC- or LC-MS 100 µg 10534-100 More Info
(R)-Bromoenol lactone-d7 An internal standard for the quantification of (R)-BEL by GC- or LC-MS 500 µg 10534-500 More Info
(R)-(4-Bromophenyl)(phenyl)methanamine A synthetic intermediate; has been used in the synthesis of δ-opioid… 100 mg 37310-100 More Info
(R)-(4-Bromophenyl)(phenyl)methanamine A synthetic intermediate; has been used in the synthesis of δ-opioid… 25 mg 37310-25 More Info
(R)-(4-Bromophenyl)(phenyl)methanamine A synthetic intermediate; has been used in the synthesis of δ-opioid… 50 mg 37310-50 More Info
(R)-Butaprost Butaprost is a structural analog of PGE2 with good selectivity for the EP2… 1 mg 13745-1 More Info
(R)-Butaprost Butaprost is a structural analog of PGE2 with good selectivity for the EP2… 10 mg 13745-10 More Info
(R)-Butaprost Butaprost is a structural analog of PGE2 with good selectivity for the EP2… 5 mg 13745-5 More Info
(R)-Butaprost (free acid) A C-16 epimer of butaprost, a selective EP2 receptor agonist 1 mg 10006045-1 More Info
(R)-Butaprost (free acid) A C-16 epimer of butaprost, a selective EP2 receptor agonist 10 mg 10006045-10 More Info
(R)-Butaprost (free acid) A C-16 epimer of butaprost, a selective EP2 receptor agonist 5 mg 10006045-5 More Info
(R)-Butaprost (free acid) A C-16 epimer of butaprost, a selective EP2 receptor agonist 500 µg 10006045-500 More Info
RC363 An inhibitor of ferroptosis; reduces DPPH radicals by ~40% in a cell-free… 1 mg 31407-1 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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