CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 534 of 652
Non-Antibody Products
Page 534 of 652
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Rilmenidine | An antihypertensive agent; binds to imidazole receptors in bovine rostral… | 100 mg | 32879-100 | More Info |
| Rilmenidine | An antihypertensive agent; binds to imidazole receptors in bovine rostral… | 500 mg | 32879-500 | More Info |
| Rilmenidine-d4 | An internal standard for the quantification of rilmenidine by GC- or LC-MS | 1 mg | 31691-1 | More Info |
| Rilmenidine-d4 | An internal standard for the quantification of rilmenidine by GC- or LC-MS | 500 µg | 31691-500 | More Info |
| Rilmenidine (hemifumarate) | An antihypertensive agent; binds to imidazole receptors in bovine rostral… | 1 mg | 16988-1 | More Info |
| Rilmenidine (hemifumarate) | An antihypertensive agent; binds to imidazole receptors in bovine rostral… | 10 mg | 16988-10 | More Info |
| Rilmenidine (hemifumarate) | An antihypertensive agent; binds to imidazole receptors in bovine rostral… | 5 mg | 16988-5 | More Info |
| Rilmenidine (hemifumarate) | An antihypertensive agent; binds to imidazole receptors in bovine rostral… | 50 mg | 16988-50 | More Info |
| 15(R)-Iloprost | The inverted C-15 epimer of iloprost | 1 mg | 10043-1 | More Info |
| 15(R)-Iloprost | The inverted C-15 epimer of iloprost | 10 mg | 10043-10 | More Info |
| 15(R)-Iloprost | The inverted C-15 epimer of iloprost | 5 mg | 10043-5 | More Info |
| 15(R)-Iloprost | The inverted C-15 epimer of iloprost | 500 µg | 10043-500 | More Info |
| 16(R)-Iloprost | An isomer of iloprost that inhibits platelet aggregation with an IC 50 val… | 1 mg | 13076-1 | More Info |
| 16(R)-Iloprost | An isomer of iloprost that inhibits platelet aggregation with an IC 50 val… | 5 mg | 13076-5 | More Info |
| 16(R)-Iloprost | An isomer of iloprost that inhibits platelet aggregation with an IC 50 val… | 500 µg | 13076-500 | More Info |
| Rilpivirine | A non-nucleoside reverse transcriptase inhibitor; inhibits growth of wild-… | 1 mg | 21559-1 | More Info |
| Rilpivirine | A non-nucleoside reverse transcriptase inhibitor; inhibits growth of wild-… | 10 mg | 21559-10 | More Info |
| Rilpivirine | A non-nucleoside reverse transcriptase inhibitor; inhibits growth of wild-… | 25 mg | 21559-25 | More Info |
| Rilpivirine | A non-nucleoside reverse transcriptase inhibitor; inhibits growth of wild-… | 5 mg | 21559-5 | More Info |
| Rilpivirine-d6 (hydrochloride) | An internal standard for the quantification of rilpivirine by GC- or LC-MS… | 1 mg | 26520-1 | More Info |
| Rilpivirine-d6 (hydrochloride) | An internal standard for the quantification of rilpivirine by GC- or LC-MS… | 500 µg | 26520-500 | More Info |
| Riluzole | A calcium channel inhibitor; selective for the voltage-gated calcium chann… | 10 mg | 35833-10 | More Info |
| Riluzole | A calcium channel inhibitor; selective for the voltage-gated calcium chann… | 100 mg | 35833-100 | More Info |
| Riluzole | A calcium channel inhibitor; selective for the voltage-gated calcium chann… | 250 mg | 35833-250 | More Info |
| Riluzole | A calcium channel inhibitor; selective for the voltage-gated calcium chann… | 50 mg | 35833-50 | More Info |
| Riluzole-13C,15N2 | An internal standard for the quantification of riluzole by GC- or LC-MS | 1 mg | 25361-1 | More Info |
| Riluzole (hydrochloride) | A benzothiazole derivative with anti-excitotoxic effects that acts by bloc… | 10 mg | 14577-10 | More Info |
| Riluzole (hydrochloride) | A benzothiazole derivative with anti-excitotoxic effects that acts by bloc… | 50 mg | 14577-50 | More Info |
| Rimantadine (hydrochloride) | A derivative of amantadine with antiviral activity; inhibits recombinant i… | 100 mg | 23838-100 | More Info |
| Rimantadine (hydrochloride) | A derivative of amantadine with antiviral activity; inhibits recombinant i… | 25 mg | 23838-25 | More Info |
| Rimantadine (hydrochloride) | A derivative of amantadine with antiviral activity; inhibits recombinant i… | 250 mg | 23838-250 | More Info |
| Rimantadine (hydrochloride) | A derivative of amantadine with antiviral activity; inhibits recombinant i… | 50 mg | 23838-50 | More Info |
| Rimiducid | A CID for FKBPF36V fusion proteins; selectively binds to FKBPF36V over wil… | 1 mg | 35303-1 | More Info |
| Rimiducid | A CID for FKBPF36V fusion proteins; selectively binds to FKBPF36V over wil… | 10 mg | 35303-10 | More Info |
| Rimiducid | A CID for FKBPF36V fusion proteins; selectively binds to FKBPF36V over wil… | 5 mg | 35303-5 | More Info |
| Rimonabant | A CB1 receptor antagonist (Ki = 5.6 nM); selective for CB1 over CB2 recept… | 10 mg | 9000484-10 | More Info |
| Rimonabant | A CB1 receptor antagonist (Ki = 5.6 nM); selective for CB1 over CB2 recept… | 25 mg | 9000484-25 | More Info |
| Rimonabant | A CB1 receptor antagonist (Ki = 5.6 nM); selective for CB1 over CB2 recept… | 5 mg | 9000484-5 | More Info |
| Rimonabant | A CB1 receptor antagonist (Ki = 5.6 nM); selective for CB1 over CB2 recept… | 50 mg | 9000484-50 | More Info |
| Rimonabant-d10 | An internal standard for the quantification of rimonabant by GC- or LC-MS | 1 mg | 9001821-1 | More Info |
| Rimonabant-d10 | An internal standard for the quantification of rimonabant by GC- or LC-MS | 500 µg | 9001821-500 | More Info |
| (R)-IMPP | A cell-permeable inhibitor of PCSK9 secretion (IC50 = 4.8 µM); promo… | 1 mg | 20861-1 | More Info |
| (R)-IMPP | A cell-permeable inhibitor of PCSK9 secretion (IC50 = 4.8 µM); promo… | 10 mg | 20861-10 | More Info |
| (R)-IMPP | A cell-permeable inhibitor of PCSK9 secretion (IC50 = 4.8 µM); promo… | 25 mg | 20861-25 | More Info |
| (R)-IMPP | A cell-permeable inhibitor of PCSK9 secretion (IC50 = 4.8 µM); promo… | 5 mg | 20861-5 | More Info |
| Riociguat | A stimulator of sGC; stimulates recombinant sGC in a concentration-depende… | 10 mg | 9000554-10 | More Info |
| Riociguat | A stimulator of sGC; stimulates recombinant sGC in a concentration-depende… | 25 mg | 9000554-25 | More Info |
| Riociguat | A stimulator of sGC; stimulates recombinant sGC in a concentration-depende… | 5 mg | 9000554-5 | More Info |
| Riociguat | A stimulator of sGC; stimulates recombinant sGC in a concentration-depende… | 50 mg | 9000554-50 | More Info |
| Riociguat-13C-d3 | An internal standard for the quantification of riociguat by GC- or LC-MS | 1 mg | 25314-1 | More Info |
| Riociguat-13C-d3 | An internal standard for the quantification of riociguat by GC- or LC-MS | 500 µg | 25314-500 | More Info |
| RIPA-56 | A RIPK1 inhibitor (IC50 = 13 nM); selective for RIPK1 over RIPK3 at 10 &mi… | 10 mg | 33431-10 | More Info |
| RIPA-56 | A RIPK1 inhibitor (IC50 = 13 nM); selective for RIPK1 over RIPK3 at 10 &mi… | 25 mg | 33431-25 | More Info |
| RIPA-56 | A RIPK1 inhibitor (IC50 = 13 nM); selective for RIPK1 over RIPK3 at 10 &mi… | 5 mg | 33431-5 | More Info |
| RIPA-56 | A RIPK1 inhibitor (IC50 = 13 nM); selective for RIPK1 over RIPK3 at 10 &mi… | 50 mg | 33431-50 | More Info |
| RIPA Buffer Concentrate | A concentrated buffer solution | 1 ea | 10010263-1 | More Info |
| Ripasudil (hydrochloride hydrate) | A ROCK1 and ROCK2 inhibitor (IC50s = 51 and 19 nM, respectively); selectiv… | 1 mg | 19920-1 | More Info |
| Ripasudil (hydrochloride hydrate) | A ROCK1 and ROCK2 inhibitor (IC50s = 51 and 19 nM, respectively); selectiv… | 10 mg | 19920-10 | More Info |
| Ripasudil (hydrochloride hydrate) | A ROCK1 and ROCK2 inhibitor (IC50s = 51 and 19 nM, respectively); selectiv… | 25 mg | 19920-25 | More Info |
| Ripasudil (hydrochloride hydrate) | A ROCK1 and ROCK2 inhibitor (IC50s = 51 and 19 nM, respectively); selectiv… | 5 mg | 19920-5 | More Info |
| RIPGBM | A prodrug form of the pro-apoptotic compound cRIPGBM; converted to cRIPGBM… | 1 mg | 27860-1 | More Info |
| RIPGBM | A prodrug form of the pro-apoptotic compound cRIPGBM; converted to cRIPGBM… | 10 mg | 27860-10 | More Info |
| RIPGBM | A prodrug form of the pro-apoptotic compound cRIPGBM; converted to cRIPGBM… | 5 mg | 27860-5 | More Info |
| Ripretinib | A KIT and PDGFRα inhibitor (IC50s = 3 and 3.6 nM, respectively); sel… | 10 mg | 33782-10 | More Info |
| Ripretinib | A KIT and PDGFRα inhibitor (IC50s = 3 and 3.6 nM, respectively); sel… | 25 mg | 33782-25 | More Info |
| Ripretinib | A KIT and PDGFRα inhibitor (IC50s = 3 and 3.6 nM, respectively); sel… | 5 mg | 33782-5 | More Info |
| Ripretinib | A KIT and PDGFRα inhibitor (IC50s = 3 and 3.6 nM, respectively); sel… | 50 mg | 33782-50 | More Info |
| Risdiplam | A SMN2 splicing modifier; enhances SMN2 splicing (EC1.5x= 40 nM) and incre… | 1 mg | 29028-1 | More Info |
| Risdiplam | A SMN2 splicing modifier; enhances SMN2 splicing (EC1.5x= 40 nM) and incre… | 10 mg | 29028-10 | More Info |
| Risdiplam | A SMN2 splicing modifier; enhances SMN2 splicing (EC1.5x= 40 nM) and incre… | 25 mg | 29028-25 | More Info |
| Risdiplam | A SMN2 splicing modifier; enhances SMN2 splicing (EC1.5x= 40 nM) and incre… | 5 mg | 29028-5 | More Info |
| Risedronate (sodium salt) | An aminobisphosphonate and antimalarial agent that inhibits bone resorptio… | 1 g | 20740-1 | More Info |
| Risedronate (sodium salt) | An aminobisphosphonate and antimalarial agent that inhibits bone resorptio… | 250 mg | 20740-250 | More Info |
| Risedronate (sodium salt) | An aminobisphosphonate and antimalarial agent that inhibits bone resorptio… | 5 g | 20740-5 | More Info |
| Risedronate (sodium salt) | An aminobisphosphonate and antimalarial agent that inhibits bone resorptio… | 500 mg | 20740-500 | More Info |
| Risperidone | An atypical antipsychotic; binds to dopamine D2 receptors (Ki = 3 nM) and… | 10 mg | 13629-10 | More Info |
| Risperidone | An atypical antipsychotic; binds to dopamine D2 receptors (Ki = 3 nM) and… | 100 mg | 13629-100 | More Info |
| Risperidone | An atypical antipsychotic; binds to dopamine D2 receptors (Ki = 3 nM) and… | 50 mg | 13629-50 | More Info |
| Risperidone-d4 | An internal standard for the quantification of risperidone by GC- or LC-MS | 1 mg | 10010570-1 | More Info |
| Risperidone-d4 | An internal standard for the quantification of risperidone by GC- or LC-MS | 500 µg | 10010570-500 | More Info |
| Risperidone E-oxime | An impurity found in risperidone | 1 mg | 22156-1 | More Info |
| Risperidone E-oxime | An impurity found in risperidone | 10 mg | 22156-10 | More Info |
| Risperidone E-oxime | An impurity found in risperidone | 5 mg | 22156-5 | More Info |
| Risperidone E-oxime | An impurity found in risperidone | 500 µg | 22156-500 | More Info |
| Ristocetin A (sulfate) | An antibiotic used in the ristocetin cofactor assay and the ristocetin-ind… | 10 mg | 20601-10 | More Info |
| Ristocetin A (sulfate) | An antibiotic used in the ristocetin cofactor assay and the ristocetin-ind… | 50 mg | 20601-50 | More Info |
| Risuteganib (trifluoroacetate salt) | An anti-integrin peptide; protects against hydroquinone-induced necrosis a… | 1 mg | 33303-1 | More Info |
| Risuteganib (trifluoroacetate salt) | An anti-integrin peptide; protects against hydroquinone-induced necrosis a… | 10 mg | 33303-10 | More Info |
| Risuteganib (trifluoroacetate salt) | An anti-integrin peptide; protects against hydroquinone-induced necrosis a… | 5 mg | 33303-5 | More Info |
| RITA | An inhibitor of p53-HDM-2 interaction; reactivates the tumor suppressor fu… | 1 mg | 10006426-1 | More Info |
| RITA | An inhibitor of p53-HDM-2 interaction; reactivates the tumor suppressor fu… | 10 mg | 10006426-10 | More Info |
| RITA | An inhibitor of p53-HDM-2 interaction; reactivates the tumor suppressor fu… | 5 mg | 10006426-5 | More Info |
| RITA | An inhibitor of p53-HDM-2 interaction; reactivates the tumor suppressor fu… | 50 mg | 10006426-50 | More Info |
| Ritalinic Acid | An inactive, major metabolite of methylphenidate; intended for forensic an… | 10 mg | 15915-10 | More Info |
| Ritalinic Acid | An inactive, major metabolite of methylphenidate; intended for forensic an… | 5 mg | 15915-5 | More Info |
| Ritalinic Acid | An inactive, major metabolite of methylphenidate; intended for forensic an… | 50 mg | 15915-50 | More Info |
| Ritanserin | A potent 5-HT2A receptor antagonist; selective for 5-HT2A over 5-HT1 recep… | 10 mg | 21374-10 | More Info |
| Ritanserin | A potent 5-HT2A receptor antagonist; selective for 5-HT2A over 5-HT1 recep… | 25 mg | 21374-25 | More Info |
| Ritanserin | A potent 5-HT2A receptor antagonist; selective for 5-HT2A over 5-HT1 recep… | 5 mg | 21374-5 | More Info |
| Ritodrine (hydrochloride) | A β2-AR agonist; induces relaxation of isolated pig detrusor muscle f… | 1 g | 26084-1 | 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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