CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 646 of 649
Non-Antibody Products
Page 646 of 649
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 10 mg | 31485-10 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 25 mg | 31485-25 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 5 mg | 31485-5 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 50 mg | 31485-50 | More Info |
| ZLY28 | An FXR agonist and inhibitor of FABP1; selectively induces reporter gene e… | 1 mg | 38864-1 | More Info |
| ZLY28 | An FXR agonist and inhibitor of FABP1; selectively induces reporter gene e… | 5 mg | 38864-5 | More Info |
| Z-Lys-OBzl (benzenesulfonate) | An amino acid-containing building block | 1 g | 30916-1 | More Info |
| Z-Lys-OBzl (benzenesulfonate) | An amino acid-containing building block | 500 mg | 30916-500 | More Info |
| Z-Lys-OH | An amino acid building block; has been used in the synthesis of peptidomim… | 1 g | 30460-1 | More Info |
| Z-Lys-OH | An amino acid building block; has been used in the synthesis of peptidomim… | 10 g | 30460-10 | More Info |
| Z-Lys-OH | An amino acid building block; has been used in the synthesis of peptidomim… | 5 g | 30460-5 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 1 g | 30804-1 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 100 mg | 30804-100 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 250 mg | 30804-250 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 500 mg | 30804-500 | More Info |
| ZM 241385 | A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… | 1 mg | 20447-1 | More Info |
| ZM 241385 | A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… | 10 mg | 20447-10 | More Info |
| ZM 241385 | A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… | 25 mg | 20447-25 | More Info |
| ZM 241385 | A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… | 5 mg | 20447-5 | More Info |
| ZM 306416 | Inhibits KDR and Flt VEGF receptors with IC50 values of 100 nM and 2 &micr… | 1 mg | 16968-1 | More Info |
| ZM 306416 | Inhibits KDR and Flt VEGF receptors with IC50 values of 100 nM and 2 &micr… | 10 mg | 16968-10 | More Info |
| ZM 306416 | Inhibits KDR and Flt VEGF receptors with IC50 values of 100 nM and 2 &micr… | 5 mg | 16968-5 | More Info |
| ZM 336372 | A potent ATP-competitive inhibitor of Raf-1 in vitro (IC50 = 70 nM) with t… | 1 mg | 10010367-1 | More Info |
| ZM 336372 | A potent ATP-competitive inhibitor of Raf-1 in vitro (IC50 = 70 nM) with t… | 10 mg | 10010367-10 | More Info |
| ZM 336372 | A potent ATP-competitive inhibitor of Raf-1 in vitro (IC50 = 70 nM) with t… | 25 mg | 10010367-25 | More Info |
| ZM 336372 | A potent ATP-competitive inhibitor of Raf-1 in vitro (IC50 = 70 nM) with t… | 5 mg | 10010367-5 | More Info |
| ZM 447439 | A selective inhibitor of Aurora B kinase (IC50 = 10 µM), less potent… | 10 mg | 13601-10 | More Info |
| ZM 447439 | A selective inhibitor of Aurora B kinase (IC50 = 10 µM), less potent… | 5 mg | 13601-5 | More Info |
| ZM 447439 | A selective inhibitor of Aurora B kinase (IC50 = 10 µM), less potent… | 50 mg | 13601-50 | More Info |
| ZM 449829 | An inhibitor of JAK3 (IC50 = 0.158 µM) and a degradation product of… | 10 mg | 32820-10 | More Info |
| ZM 449829 | An inhibitor of JAK3 (IC50 = 0.158 µM) and a degradation product of… | 25 mg | 32820-25 | More Info |
| ZM 449829 | An inhibitor of JAK3 (IC50 = 0.158 µM) and a degradation product of… | 5 mg | 32820-5 | More Info |
| ZM 449829 | An inhibitor of JAK3 (IC50 = 0.158 µM) and a degradation product of… | 50 mg | 32820-50 | More Info |
| ZM 522 | An inhibitor of ecto-5'-nucleotidase (IC50s = 0.56 and 3.06 µM for t… | 100 mg | 37904-100 | More Info |
| ZM 522 | An inhibitor of ecto-5'-nucleotidase (IC50s = 0.56 and 3.06 µM for t… | 25 mg | 37904-25 | More Info |
| ZM 522 | An inhibitor of ecto-5'-nucleotidase (IC50s = 0.56 and 3.06 µM for t… | 50 mg | 37904-50 | More Info |
| ZM 323881 (hydrochloride) | A potent and selective VEGFR2 inhibitor; selective for VEGFR2 over VEGFR1,… | 1 mg | 21347-1 | More Info |
| ZM 323881 (hydrochloride) | A potent and selective VEGFR2 inhibitor; selective for VEGFR2 over VEGFR1,… | 10 mg | 21347-10 | More Info |
| ZM 323881 (hydrochloride) | A potent and selective VEGFR2 inhibitor; selective for VEGFR2 over VEGFR1,… | 25 mg | 21347-25 | More Info |
| ZM 323881 (hydrochloride) | A potent and selective VEGFR2 inhibitor; selective for VEGFR2 over VEGFR1,… | 5 mg | 21347-5 | More Info |
| ZM 39923 (hydrochloride) | An inhibitor of JAK3 (IC50 = 79 nM); also inhibits the transglutaminases T… | 1 mg | 16729-1 | More Info |
| ZM 39923 (hydrochloride) | An inhibitor of JAK3 (IC50 = 79 nM); also inhibits the transglutaminases T… | 10 mg | 16729-10 | More Info |
| ZM 39923 (hydrochloride) | An inhibitor of JAK3 (IC50 = 79 nM); also inhibits the transglutaminases T… | 5 mg | 16729-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Adrenoyl-sn-glycero-3-PC | A plasmalogen | 1 mg | 37133-1 | More Info |
| 1-1(Z)-Octadecenyl-2-Adrenoyl-sn-glycero-3-PC | A plasmalogen | 5 mg | 37133-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Adrenoyl-sn-glycero-3-PC | A plasmalogen | 500 µg | 37133-500 | More Info |
| 1-1(Z)-Octadecenyl-2-Adrenoyl-sn-glycero-3-PE | A plasmalogen; has been found in L. lactis lipid extracts | 1 mg | 37136-1 | More Info |
| 1-1(Z)-Octadecenyl-2-Adrenoyl-sn-glycero-3-PE | A plasmalogen; has been found in L. lactis lipid extracts | 5 mg | 37136-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Adrenoyl-sn-glycero-3-PE | A plasmalogen; has been found in L. lactis lipid extracts | 500 µg | 37136-500 | More Info |
| 1-1(Z)-Octadecenyl-2-Arachidonoyl-sn-glycero-3-PC | A plasmalogen; scavenges singlet oxygen in a cell-free assay | 1 mg | 37132-1 | More Info |
| 1-1(Z)-Octadecenyl-2-Arachidonoyl-sn-glycero-3-PC | A plasmalogen; scavenges singlet oxygen in a cell-free assay | 5 mg | 37132-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Arachidonoyl-sn-glycero-3-PC | A plasmalogen; scavenges singlet oxygen in a cell-free assay | 500 µg | 37132-500 | More Info |
| 1-1(Z)-Octadecenyl-2-Arachidonoyl-sn-glycero-3-PE | A plasmalogen; has been found in chicken breast meat,, | 1 mg | 37137-1 | More Info |
| 1-1(Z)-Octadecenyl-2-Arachidonoyl-sn-glycero-3-PE | A plasmalogen; has been found in chicken breast meat,, | 5 mg | 37137-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Arachidonoyl-sn-glycero-3-PE | A plasmalogen; has been found in chicken breast meat,, | 500 µg | 37137-500 | More Info |
| 1-1(Z)-Octadecenyl-2-Docosahexaenoyl-sn-glycero-3-PC | A plasmalogen; has been found in bovine retina and fish viscera | 1 mg | 37134-1 | More Info |
| 1-1(Z)-Octadecenyl-2-Docosahexaenoyl-sn-glycero-3-PC | A plasmalogen; has been found in bovine retina and fish viscera | 5 mg | 37134-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Docosahexaenoyl-sn-glycero-3-PE | A plasmalogen; has been found in chicken breast meat | 1 mg | 37138-1 | More Info |
| 1-1(Z)-Octadecenyl-2-Docosahexaenoyl-sn-glycero-3-PE | A plasmalogen; has been found in chicken breast meat | 5 mg | 37138-5 | More Info |
| 1-1(Z)-Octadecenyl-2-Docosahexaenoyl-sn-glycero-3-PE | A plasmalogen; has been found in chicken breast meat | 500 µg | 37138-500 | More Info |
| Zofenoprilat | An ACE inhibitor (IC50 = 8 nM for the rabbit lung enzyme) and active metab… | 1 mg | 38124-1 | More Info |
| Zofenoprilat | An ACE inhibitor (IC50 = 8 nM for the rabbit lung enzyme) and active metab… | 5 mg | 38124-5 | More Info |
| Zofenoprilat | An ACE inhibitor (IC50 = 8 nM for the rabbit lung enzyme) and active metab… | 500 µg | 38124-500 | More Info |
| Zofenopril (calcium salt) | A prodrug form of zofenoprilat; an ACE inhibitor (IC50 = 0.9 nM in heart t… | 10 mg | 29525-10 | More Info |
| Zofenopril (calcium salt) | A prodrug form of zofenoprilat; an ACE inhibitor (IC50 = 0.9 nM in heart t… | 25 mg | 29525-25 | More Info |
| Zofenopril (calcium salt) | A prodrug form of zofenoprilat; an ACE inhibitor (IC50 = 0.9 nM in heart t… | 5 mg | 29525-5 | More Info |
| Zolazepam | An analytical reference standard categorized as pyrazolodiazepinone; has a… | 1 mg | 21128-1 | More Info |
| Zolazepam | An analytical reference standard categorized as pyrazolodiazepinone; has a… | 5 mg | 21128-5 | More Info |
| Zoledronic Acid (hydrate) | A third-generation heterocyclic nitrogen-containing bisphosphonate that in… | 100 mg | 14984-100 | More Info |
| Zoledronic Acid (hydrate) | A third-generation heterocyclic nitrogen-containing bisphosphonate that in… | 25 mg | 14984-25 | More Info |
| Zoledronic Acid (hydrate) | A third-generation heterocyclic nitrogen-containing bisphosphonate that in… | 50 mg | 14984-50 | More Info |
| Zoliflodacin | A fluoroquinolone antibiotic; inhibits bacterial DNA gyrase supercoiling a… | 1 mg | 34203-1 | More Info |
| Zoliflodacin | A fluoroquinolone antibiotic; inhibits bacterial DNA gyrase supercoiling a… | 10 mg | 34203-10 | More Info |
| Zoliflodacin | A fluoroquinolone antibiotic; inhibits bacterial DNA gyrase supercoiling a… | 25 mg | 34203-25 | More Info |
| Zoliflodacin | A fluoroquinolone antibiotic; inhibits bacterial DNA gyrase supercoiling a… | 5 mg | 34203-5 | More Info |
| Zolmitriptan | A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… | 10 mg | 15871-10 | More Info |
| Zolmitriptan | A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… | 25 mg | 15871-25 | More Info |
| Zolmitriptan | A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… | 5 mg | 15871-5 | More Info |
| Zolmitriptan | A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… | 50 mg | 15871-50 | More Info |
| Zoniporide (hydrochloride) | Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… | 1 mg | 16004-1 | More Info |
| Zoniporide (hydrochloride) | Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… | 10 mg | 16004-10 | More Info |
| Zoniporide (hydrochloride) | Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… | 5 mg | 16004-5 | More Info |
| Zoniporide (hydrochloride) | Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… | 50 mg | 16004-50 | More Info |
| Zonisamide | A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… | 1 g | 24183-1 | More Info |
| Zonisamide | A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… | 100 mg | 24183-100 | More Info |
| Zonisamide | A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… | 250 mg | 24183-250 | More Info |
| Zonisamide | A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… | 500 mg | 24183-500 | More Info |
| Zonisamide-13C2,15N | An internal standard for the quantification of zonisamide by GC- or LC-MS | 1 mg | 28807-1 | More Info |
| Zopolrestat | A potent aldose reductase inhibitor (IC50s = 1.9 and 41 nM for the human p… | 1 mg | 29185-1 | More Info |
| Zopolrestat | A potent aldose reductase inhibitor (IC50s = 1.9 and 41 nM for the human p… | 10 mg | 29185-10 | More Info |
| Zopolrestat | A potent aldose reductase inhibitor (IC50s = 1.9 and 41 nM for the human p… | 5 mg | 29185-5 | More Info |
| Zosuquidar (hydrochloride) | A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… | 1 mg | 21533-1 | More Info |
| Zosuquidar (hydrochloride) | A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… | 10 mg | 21533-10 | More Info |
| Zosuquidar (hydrochloride) | A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… | 25 mg | 21533-25 | More Info |
| Zosuquidar (hydrochloride) | A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… | 5 mg | 21533-5 | More Info |
| Zotarolimus | A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… | 1 mg | 29246-1 | More Info |
| Zotarolimus | A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… | 10 mg | 29246-10 | More Info |
| Zotarolimus | A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… | 25 mg | 29246-25 | More Info |
| Zotarolimus | A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… | 5 mg | 29246-5 | More Info |
| Zotepine | An atypical antipsychotic; a dopamine D2 and D3 receptor antagonist (Kis =… | 10 mg | 23909-10 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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Ann Arbor MI 48108
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