CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 769 of 1
Non-Antibody Products
Page 769 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| ML-289 | A negative allosteric modulator of mGlu3 (IC50 = 0.66 µM) that displ… | 5 mg | 15195-5 | More Info |
| ML-290 | An RXFP1 agonist (EC50 = 0.094 µM for the human receptor in a cAMP p… | 1 mg | 21134-1 | More Info |
| ML-290 | An RXFP1 agonist (EC50 = 0.094 µM for the human receptor in a cAMP p… | 10 mg | 21134-10 | More Info |
| ML-290 | An RXFP1 agonist (EC50 = 0.094 µM for the human receptor in a cAMP p… | 5 mg | 21134-5 | More Info |
| ML-291 | A novel activator of the apoptotic arm of the UPR, but not the adaptive arm | 1 mg | 19831-1 | More Info |
| ML-291 | A novel activator of the apoptotic arm of the UPR, but not the adaptive arm | 10 mg | 19831-10 | More Info |
| ML-291 | A novel activator of the apoptotic arm of the UPR, but not the adaptive arm | 25 mg | 19831-25 | More Info |
| ML-291 | A novel activator of the apoptotic arm of the UPR, but not the adaptive arm | 5 mg | 19831-5 | More Info |
| ML-297 | A selective GIRK1 / 2 activator (EC50s = 0.16 and 1.8 µM for GIRK1 /… | 1 mg | 14792-1 | More Info |
| ML-297 | A selective GIRK1 / 2 activator (EC50s = 0.16 and 1.8 µM for GIRK1 /… | 10 mg | 14792-10 | More Info |
| ML-297 | A selective GIRK1 / 2 activator (EC50s = 0.16 and 1.8 µM for GIRK1 /… | 25 mg | 14792-25 | More Info |
| ML-297 | A selective GIRK1 / 2 activator (EC50s = 0.16 and 1.8 µM for GIRK1 /… | 5 mg | 14792-5 | More Info |
| ML-298 | A selective inhibitor of PLD2 (IC50 = 355 nM); decreases invasive migratio… | 1 mg | 15349-1 | More Info |
| ML-298 | A selective inhibitor of PLD2 (IC50 = 355 nM); decreases invasive migratio… | 10 mg | 15349-10 | More Info |
| ML-298 | A selective inhibitor of PLD2 (IC50 = 355 nM); decreases invasive migratio… | 5 mg | 15349-5 | More Info |
| ML-299 | A dual inhibitor of PLD1 and PLD2 (IC50s = 6 and 20 nM, respectively); sel… | 1 mg | 17632-1 | More Info |
| ML-299 | A dual inhibitor of PLD1 and PLD2 (IC50s = 6 and 20 nM, respectively); sel… | 5 mg | 17632-5 | More Info |
| ML-299 | A dual inhibitor of PLD1 and PLD2 (IC50s = 6 and 20 nM, respectively); sel… | 500 µg | 17632-500 | More Info |
| ML-311 | An inhibitor of Mcl-1 (IC50 = 0.31 µM in a fluorescence polarization… | 1 mg | 29445-1 | More Info |
| ML-311 | An inhibitor of Mcl-1 (IC50 = 0.31 µM in a fluorescence polarization… | 10 mg | 29445-10 | More Info |
| ML-311 | An inhibitor of Mcl-1 (IC50 = 0.31 µM in a fluorescence polarization… | 5 mg | 29445-5 | More Info |
| ML-314 | An NTS1 agonist; selective for NTS1 over NTS2 in a cell-based assay of rec… | 1 mg | 19550-1 | More Info |
| ML-314 | An NTS1 agonist; selective for NTS1 over NTS2 in a cell-based assay of rec… | 10 mg | 19550-10 | More Info |
| ML-314 | An NTS1 agonist; selective for NTS1 over NTS2 in a cell-based assay of rec… | 25 mg | 19550-25 | More Info |
| ML-314 | An NTS1 agonist; selective for NTS1 over NTS2 in a cell-based assay of rec… | 5 mg | 19550-5 | More Info |
| ML-323 | A selective inhibitor of the USP1-UAF1 deubiquitinase complex activity (IC… | 10 mg | 18010-10 | More Info |
| ML-323 | A selective inhibitor of the USP1-UAF1 deubiquitinase complex activity (IC… | 25 mg | 18010-25 | More Info |
| ML-323 | A selective inhibitor of the USP1-UAF1 deubiquitinase complex activity (IC… | 5 mg | 18010-5 | More Info |
| ML-323 | A selective inhibitor of the USP1-UAF1 deubiquitinase complex activity (IC… | 50 mg | 18010-50 | More Info |
| ML-324 | A cell-permeable inhibitor of JMJD2E (KDM4DL; IC50 = 920 nM); reduces the… | 1 mg | 17472-1 | More Info |
| ML-324 | A cell-permeable inhibitor of JMJD2E (KDM4DL; IC50 = 920 nM); reduces the… | 10 mg | 17472-10 | More Info |
| ML-324 | A cell-permeable inhibitor of JMJD2E (KDM4DL; IC50 = 920 nM); reduces the… | 25 mg | 17472-25 | More Info |
| ML-324 | A cell-permeable inhibitor of JMJD2E (KDM4DL; IC50 = 920 nM); reduces the… | 5 mg | 17472-5 | More Info |
| ML-329 | An inhibitor of the MITF pathway (IC50 = 1.2 µM for TRPM-1 promoter… | 1 mg | 22481-1 | More Info |
| ML-329 | An inhibitor of the MITF pathway (IC50 = 1.2 µM for TRPM-1 promoter… | 10 mg | 22481-10 | More Info |
| ML-329 | An inhibitor of the MITF pathway (IC50 = 1.2 µM for TRPM-1 promoter… | 5 mg | 22481-5 | More Info |
| ML-334 | An inhibitor of the Nrf2-Keap1 protein-protein interaction; binds to the K… | 1 mg | 31439-1 | More Info |
| ML-334 | An inhibitor of the Nrf2-Keap1 protein-protein interaction; binds to the K… | 10 mg | 31439-10 | More Info |
| ML-334 | An inhibitor of the Nrf2-Keap1 protein-protein interaction; binds to the K… | 5 mg | 31439-5 | More Info |
| ML-335 | The first identified agonist for OPRM1-OPRD1 heterodimerization (EC50 = 40… | 1 mg | 15196-1 | More Info |
| ML-335 | The first identified agonist for OPRM1-OPRD1 heterodimerization (EC50 = 40… | 10 mg | 15196-10 | More Info |
| ML-335 | The first identified agonist for OPRM1-OPRD1 heterodimerization (EC50 = 40… | 25 mg | 15196-25 | More Info |
| ML-335 | The first identified agonist for OPRM1-OPRD1 heterodimerization (EC50 = 40… | 5 mg | 15196-5 | More Info |
| ML-335 | An activator of K2P2.1 / TREK1 and K2P10.1 / TREK2 (EC50s = 14.3 and 5.2 &… | 10 mg | 27635-10 | More Info |
| ML-335 | An activator of K2P2.1 / TREK1 and K2P10.1 / TREK2 (EC50s = 14.3 and 5.2 &… | 25 mg | 27635-25 | More Info |
| ML-335 | An activator of K2P2.1 / TREK1 and K2P10.1 / TREK2 (EC50s = 14.3 and 5.2 &… | 5 mg | 27635-5 | More Info |
| ML-335 | An activator of K2P2.1 / TREK1 and K2P10.1 / TREK2 (EC50s = 14.3 and 5.2 &… | 50 mg | 27635-50 | More Info |
| ML-336 | A quinazolinone-based compound that has been shown to inhibit a VEEV-induc… | 1 mg | 9001920-1 | More Info |
| ML-336 | A quinazolinone-based compound that has been shown to inhibit a VEEV-induc… | 10 mg | 9001920-10 | More Info |
| ML-336 | A quinazolinone-based compound that has been shown to inhibit a VEEV-induc… | 25 mg | 9001920-25 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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