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
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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
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