CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 434 of 649
Non-Antibody Products
Page 434 of 649
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| (+)-Nutlin-3 | The less active enantiomer of (-)-nutlin-3; inhibits the interaction betwe… | 10 mg | 10009816-10 | More Info |
| (+)-Nutlin-3 | The less active enantiomer of (-)-nutlin-3; inhibits the interaction betwe… | 25 mg | 10009816-25 | More Info |
| (+)-Nutlin-3 | The less active enantiomer of (-)-nutlin-3; inhibits the interaction betwe… | 5 mg | 10009816-5 | More Info |
| NV-5138 | A sestrin modulator and mTORC1 activator; binds to sestrin 2 (Kd = 1.49 &m… | 1 mg | 35482-1 | More Info |
| NV-5138 | A sestrin modulator and mTORC1 activator; binds to sestrin 2 (Kd = 1.49 &m… | 10 mg | 35482-10 | More Info |
| NV-5138 | A sestrin modulator and mTORC1 activator; binds to sestrin 2 (Kd = 1.49 &m… | 5 mg | 35482-5 | More Info |
| NV-5138 | A sestrin modulator and mTORC1 activator; binds to sestrin 2 (Kd = 1.49 &m… | 500 µg | 35482-500 | More Info |
| NVP-2 | A Cdk9 / cyclin T1 complex inhibitor; selective for the Cdk9 / cyclin T1 c… | 1 mg | 34725-1 | More Info |
| NVP-2 | A Cdk9 / cyclin T1 complex inhibitor; selective for the Cdk9 / cyclin T1 c… | 10 mg | 34725-10 | More Info |
| NVP-2 | A Cdk9 / cyclin T1 complex inhibitor; selective for the Cdk9 / cyclin T1 c… | 25 mg | 34725-25 | More Info |
| NVP-2 | A Cdk9 / cyclin T1 complex inhibitor; selective for the Cdk9 / cyclin T1 c… | 5 mg | 34725-5 | More Info |
| NVP-231 | A potent and reversible inhibitor of ceramide kinase (IC50 = 12 nM); selec… | 1 mg | 13858-1 | More Info |
| NVP-231 | A potent and reversible inhibitor of ceramide kinase (IC50 = 12 nM); selec… | 10 mg | 13858-10 | More Info |
| NVP-231 | A potent and reversible inhibitor of ceramide kinase (IC50 = 12 nM); selec… | 25 mg | 13858-25 | More Info |
| NVP-231 | A potent and reversible inhibitor of ceramide kinase (IC50 = 12 nM); selec… | 5 mg | 13858-5 | More Info |
| NVP-AAM077 | An NMDA receptor antagonist (IC50 = 0.008 µM); selective for NMDA re… | 1 mg | 30622-1 | More Info |
| NVP-AAM077 | An NMDA receptor antagonist (IC50 = 0.008 µM); selective for NMDA re… | 10 mg | 30622-10 | More Info |
| NVP-AAM077 | An NMDA receptor antagonist (IC50 = 0.008 µM); selective for NMDA re… | 25 mg | 30622-25 | More Info |
| NVP-AAM077 | An NMDA receptor antagonist (IC50 = 0.008 µM); selective for NMDA re… | 5 mg | 30622-5 | More Info |
| NVP-ACC789 | An inhibitor of VEGFRs (IC50s = 0.38, 0.02, 0.18, and 0.23 µM for hu… | 1 mg | 23458-1 | More Info |
| NVP-ACC789 | An inhibitor of VEGFRs (IC50s = 0.38, 0.02, 0.18, and 0.23 µM for hu… | 10 mg | 23458-10 | More Info |
| NVP-ACC789 | An inhibitor of VEGFRs (IC50s = 0.38, 0.02, 0.18, and 0.23 µM for hu… | 5 mg | 23458-5 | More Info |
| NVP-ADW742 | A selective IGF-1R inhibitor (IC50 = 0.17 µM); inhibits tumor prolif… | 1 mg | 18390-1 | More Info |
| NVP-ADW742 | A selective IGF-1R inhibitor (IC50 = 0.17 µM); inhibits tumor prolif… | 10 mg | 18390-10 | More Info |
| NVP-ADW742 | A selective IGF-1R inhibitor (IC50 = 0.17 µM); inhibits tumor prolif… | 5 mg | 18390-5 | More Info |
| NVP-ADW742 | A selective IGF-1R inhibitor (IC50 = 0.17 µM); inhibits tumor prolif… | 50 mg | 18390-50 | More Info |
| NVP-AEW541 | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 10 mg | 33946-10 | More Info |
| NVP-AEW541 | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 25 mg | 33946-25 | More Info |
| NVP-AEW541 | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 5 mg | 33946-5 | More Info |
| NVP-AEW541 | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 50 mg | 33946-50 | More Info |
| NVP-AEW541 (hydrochloride) | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 1 mg | 13641-1 | More Info |
| NVP-AEW541 (hydrochloride) | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 10 mg | 13641-10 | More Info |
| NVP-AEW541 (hydrochloride) | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 5 mg | 13641-5 | More Info |
| NVP-AEW541 (hydrochloride) | An IGF-1R inhibitor (IC50 = 0.15 µM in a cell-free assay); selective… | 500 µg | 13641-500 | More Info |
| NVP-AUY922 | A Hsp90 inhibitor (IC50 = 21 nM in a FP binding assay) that prevents the p… | 10 mg | 10012698-10 | More Info |
| NVP-AUY922 | A Hsp90 inhibitor (IC50 = 21 nM in a FP binding assay) that prevents the p… | 5 mg | 10012698-5 | More Info |
| NVP-BAG956 | A dual PDK1 and class I PI3K inhibitor (IC50s = 245, 56, 446, 35, and 117… | 1 mg | 24195-1 | More Info |
| NVP-BAG956 | A dual PDK1 and class I PI3K inhibitor (IC50s = 245, 56, 446, 35, and 117… | 10 mg | 24195-10 | More Info |
| NVP-BAG956 | A dual PDK1 and class I PI3K inhibitor (IC50s = 245, 56, 446, 35, and 117… | 5 mg | 24195-5 | More Info |
| NVP-BEP800 | An Hsp90 inhibitor (IC50 = 58 nM for recombinant human Hsp90β); selec… | 1 mg | 18383-1 | More Info |
| NVP-BEP800 | An Hsp90 inhibitor (IC50 = 58 nM for recombinant human Hsp90β); selec… | 10 mg | 18383-10 | More Info |
| NVP-BEP800 | An Hsp90 inhibitor (IC50 = 58 nM for recombinant human Hsp90β); selec… | 5 mg | 18383-5 | More Info |
| NVP-BEP800 | An Hsp90 inhibitor (IC50 = 58 nM for recombinant human Hsp90β); selec… | 500 µg | 18383-500 | More Info |
| NVP-BEZ235 | A dual inhibitor of class I PI3Ks and mTOR (IC50s = 4, 75, 7, and 5 nM, fo… | 100 mg | 10565-100 | More Info |
| NVP-BEZ235 | A dual inhibitor of class I PI3Ks and mTOR (IC50s = 4, 75, 7, and 5 nM, fo… | 25 mg | 10565-25 | More Info |
| NVP-BEZ235 | A dual inhibitor of class I PI3Ks and mTOR (IC50s = 4, 75, 7, and 5 nM, fo… | 250 mg | 10565-250 | More Info |
| NVP-BEZ235 | A dual inhibitor of class I PI3Ks and mTOR (IC50s = 4, 75, 7, and 5 nM, fo… | 50 mg | 10565-50 | More Info |
| NVP-BEZ235 (hydrochloride) | A potent dual inhibitor of PI3K and mTOR that is well tolerated, displays… | 10 mg | 21185-10 | More Info |
| NVP-BEZ235 (hydrochloride) | A potent dual inhibitor of PI3K and mTOR that is well tolerated, displays… | 100 mg | 21185-100 | More Info |
| NVP-BEZ235 (hydrochloride) | A potent dual inhibitor of PI3K and mTOR that is well tolerated, displays… | 25 mg | 21185-25 | More Info |
| NVP-BEZ235 (hydrochloride) | A potent dual inhibitor of PI3K and mTOR that is well tolerated, displays… | 50 mg | 21185-50 | More Info |
| NVP-BGT226 | A dual PI3K and mTOR inhibitor (EC50s = 4, 63, and 38 nM for PI3Kα,… | 1 mg | 22142-1 | More Info |
| NVP-BGT226 | A dual PI3K and mTOR inhibitor (EC50s = 4, 63, and 38 nM for PI3Kα,… | 10 mg | 22142-10 | More Info |
| NVP-BGT226 | A dual PI3K and mTOR inhibitor (EC50s = 4, 63, and 38 nM for PI3Kα,… | 25 mg | 22142-25 | More Info |
| NVP-BGT226 | A dual PI3K and mTOR inhibitor (EC50s = 4, 63, and 38 nM for PI3Kα,… | 5 mg | 22142-5 | More Info |
| NVP-BHG712 | A selective, orally bioavailable inhibitor of EphB4 kinase autophosphoryla… | 1 mg | 18489-1 | More Info |
| NVP-BHG712 | A selective, orally bioavailable inhibitor of EphB4 kinase autophosphoryla… | 10 mg | 18489-10 | More Info |
| NVP-BHG712 | A selective, orally bioavailable inhibitor of EphB4 kinase autophosphoryla… | 25 mg | 18489-25 | More Info |
| NVP-BHG712 | A selective, orally bioavailable inhibitor of EphB4 kinase autophosphoryla… | 5 mg | 18489-5 | More Info |
| NVP-BKM120 | An inhibitor of the class I PI3K isoforms p110α (IC50 = 52 nM) and p… | 10 mg | 11587-10 | More Info |
| NVP-BKM120 | An inhibitor of the class I PI3K isoforms p110α (IC50 = 52 nM) and p… | 25 mg | 11587-25 | More Info |
| NVP-BKM120 | An inhibitor of the class I PI3K isoforms p110α (IC50 = 52 nM) and p… | 5 mg | 11587-5 | More Info |
| NVP-BKM120 | An inhibitor of the class I PI3K isoforms p110α (IC50 = 52 nM) and p… | 50 mg | 11587-50 | More Info |
| NVP-BSK805 (hydrochloride) | A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme… | 1 mg | 16714-1 | More Info |
| NVP-BSK805 (hydrochloride) | A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme… | 10 mg | 16714-10 | More Info |
| NVP-BSK805 (hydrochloride) | A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme… | 5 mg | 16714-5 | More Info |
| NVP-BVU972 | A Met kinase inhibitor (IC50 = 14 nM); selective for Met over a panel of 6… | 1 mg | 34495-1 | More Info |
| NVP-BVU972 | A Met kinase inhibitor (IC50 = 14 nM); selective for Met over a panel of 6… | 10 mg | 34495-10 | More Info |
| NVP-BVU972 | A Met kinase inhibitor (IC50 = 14 nM); selective for Met over a panel of 6… | 5 mg | 34495-5 | More Info |
| NVP-CGM097 | An inhibitor of the MDM2-p53 interaction (IC50 = 1.7 nM for human MDM2 in… | 1 mg | 29519-1 | More Info |
| NVP-CGM097 | An inhibitor of the MDM2-p53 interaction (IC50 = 1.7 nM for human MDM2 in… | 10 mg | 29519-10 | More Info |
| NVP-CGM097 | An inhibitor of the MDM2-p53 interaction (IC50 = 1.7 nM for human MDM2 in… | 5 mg | 29519-5 | More Info |
| NVP-TAE226 | A FAK inhibitor (IC50 = 5.5 nM) that also inhibits IGF-1R (IC50 = 0.16 &mi… | 1 mg | 17685-1 | More Info |
| NVP-TAE226 | A FAK inhibitor (IC50 = 5.5 nM) that also inhibits IGF-1R (IC50 = 0.16 &mi… | 10 mg | 17685-10 | More Info |
| NVP-TAE226 | A FAK inhibitor (IC50 = 5.5 nM) that also inhibits IGF-1R (IC50 = 0.16 &mi… | 25 mg | 17685-25 | More Info |
| NVP-TAE226 | A FAK inhibitor (IC50 = 5.5 nM) that also inhibits IGF-1R (IC50 = 0.16 &mi… | 5 mg | 17685-5 | More Info |
| NVP-TNKS656 | A TNKS2 inhibitor (IC50 = 6 nM); inhibits Wnt ligand-induced signaling in… | 1 mg | 19930-1 | More Info |
| NVP-TNKS656 | A TNKS2 inhibitor (IC50 = 6 nM); inhibits Wnt ligand-induced signaling in… | 10 mg | 19930-10 | More Info |
| NVP-TNKS656 | A TNKS2 inhibitor (IC50 = 6 nM); inhibits Wnt ligand-induced signaling in… | 5 mg | 19930-5 | More Info |
| NVP-TNKS656 | A TNKS2 inhibitor (IC50 = 6 nM); inhibits Wnt ligand-induced signaling in… | 500 µg | 19930-500 | More Info |
| NVS-CECR2-1 | A potent and selective inhibitor of CECR2 (IC50 = 0.047 µM by Alpha… | 1 mg | 18316-1 | More Info |
| NVS-CECR2-1 | A potent and selective inhibitor of CECR2 (IC50 = 0.047 µM by Alpha… | 10 mg | 18316-10 | More Info |
| NVS-CECR2-1 | A potent and selective inhibitor of CECR2 (IC50 = 0.047 µM by Alpha… | 25 mg | 18316-25 | More Info |
| NVS-CECR2-1 | A potent and selective inhibitor of CECR2 (IC50 = 0.047 µM by Alpha… | 5 mg | 18316-5 | More Info |
| NVS-PAK1-1 | An allosteric inhibitor of PAK1 (Kd = 7 nM); has an IC50 value of 5.2 nM i… | 10 mg | 19964-10 | More Info |
| NVS-PAK1-1 | An allosteric inhibitor of PAK1 (Kd = 7 nM); has an IC50 value of 5.2 nM i… | 25 mg | 19964-25 | More Info |
| NVS-PAK1-1 | An allosteric inhibitor of PAK1 (Kd = 7 nM); has an IC50 value of 5.2 nM i… | 5 mg | 19964-5 | More Info |
| NVS-PAK1-C | A negative control for NVS-PAK1-1 , | 1 mg | 19965-1 | More Info |
| NVS-PAK1-C | A negative control for NVS-PAK1-1 , | 5 mg | 19965-5 | More Info |
| NVS-ZP7-4 | A ZIP7 inhibitor; induces apoptosis in TALL-1 cells; increases endoplasmic… | 1 mg | 33773-1 | More Info |
| NVS-ZP7-4 | A ZIP7 inhibitor; induces apoptosis in TALL-1 cells; increases endoplasmic… | 10 mg | 33773-10 | More Info |
| NVS-ZP7-4 | A ZIP7 inhibitor; induces apoptosis in TALL-1 cells; increases endoplasmic… | 25 mg | 33773-25 | More Info |
| NVS-ZP7-4 | A ZIP7 inhibitor; induces apoptosis in TALL-1 cells; increases endoplasmic… | 5 mg | 33773-5 | More Info |
| NXY-059 | A nitrone free radical spin trap with neuroprotective properties; inhibits… | 10 mg | 22109-10 | More Info |
| NXY-059 | A nitrone free radical spin trap with neuroprotective properties; inhibits… | 25 mg | 22109-25 | More Info |
| NXY-059 | A nitrone free radical spin trap with neuroprotective properties; inhibits… | 5 mg | 22109-5 | More Info |
| NXY-059 | A nitrone free radical spin trap with neuroprotective properties; inhibits… | 50 mg | 22109-50 | More Info |
| Nybomycin | A fungal metabolite with antibacterial activity; active against B. subtili… | 2.5 mg | 28099-25 | More Info |
| Nybomycin | A fungal metabolite with antibacterial activity; active against B. subtili… | 500 µg | 28099-500 | More Info |
| Nylidrin | An agonist of β-ARs and antagonist of NR1A / 2B subunit-containing NM… | 10 mg | 33232-10 | 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)
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