CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 785 of 1
Non-Antibody Products
Page 785 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| MSA-2 | A STING agonist; binds to wild-type and HAQ variant STING in a 3H-cGAMP fi… | 10 mg | 30140-10 | More Info |
| MSA-2 | A STING agonist; binds to wild-type and HAQ variant STING in a 3H-cGAMP fi… | 5 mg | 30140-5 | More Info |
| MSAB | An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… | 10 mg | 36497-10 | More Info |
| MSAB | An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… | 100 mg | 36497-100 | More Info |
| MSAB | An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… | 25 mg | 36497-25 | More Info |
| MSAB | An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… | 50 mg | 36497-50 | More Info |
| MSC2530818 | A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… | 1 mg | 29669-1 | More Info |
| MSC2530818 | A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… | 10 mg | 29669-10 | More Info |
| MSC2530818 | A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… | 25 mg | 29669-25 | More Info |
| MSC2530818 | A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… | 5 mg | 29669-5 | More Info |
| MSDC-0160 | A thiazolidinedione; inactivates MPC (IC50 = 1.2 µM) without affecti… | 1 mg | 71748-1 | More Info |
| MSDC-0160 | A thiazolidinedione; inactivates MPC (IC50 = 1.2 µM) without affecti… | 10 mg | 71748-10 | More Info |
| MSDC-0160 | A thiazolidinedione; inactivates MPC (IC50 = 1.2 µM) without affecti… | 5 mg | 71748-5 | More Info |
| MSDC-0602 | A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… | 10 mg | 27829-10 | More Info |
| MSDC-0602 | A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… | 100 mg | 27829-100 | More Info |
| MSDC-0602 | A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… | 25 mg | 27829-25 | More Info |
| MSDC-0602 | A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… | 50 mg | 27829-50 | More Info |
| MS023 (hydrochloride) | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 1 mg | 18361-1 | More Info |
| MS023 (hydrochloride) | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 10 mg | 18361-10 | More Info |
| MS023 (hydrochloride) | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 25 mg | 18361-25 | More Info |
| MS023 (hydrochloride) | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 5 mg | 18361-5 | More Info |
| MS049 (hydrochloride) | A selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM); re… | 1 mg | 18348-1 | More Info |
| MS049 (hydrochloride) | A selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM); re… | 10 mg | 18348-10 | More Info |
| MS049 (hydrochloride) | A selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM); re… | 25 mg | 18348-25 | More Info |
| MS049 (hydrochloride) | A selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM); re… | 5 mg | 18348-5 | More Info |
| MS 245 (oxalate) | An antagonist of 5-HT6 (Ki = 2.3 nM for the human recombinant receptor); s… | 1 mg | 11936-1 | More Info |
| MS 245 (oxalate) | An antagonist of 5-HT6 (Ki = 2.3 nM for the human recombinant receptor); s… | 10 mg | 11936-10 | More Info |
| MS 245 (oxalate) | An antagonist of 5-HT6 (Ki = 2.3 nM for the human recombinant receptor); s… | 5 mg | 11936-5 | More Info |
| MS-PPOH | Arachidonic acid is converted by microsomal CYP450 enzymes to a variety of… | 1 mg | 75770-1 | More Info |
| MS-PPOH | Arachidonic acid is converted by microsomal CYP450 enzymes to a variety of… | 10 mg | 75770-10 | More Info |
| MS-PPOH | Arachidonic acid is converted by microsomal CYP450 enzymes to a variety of… | 5 mg | 75770-5 | More Info |
| MS-PPOH | Arachidonic acid is converted by microsomal CYP450 enzymes to a variety of… | 50 mg | 75770-50 | More Info |
| MST-312 | A telomerase inhibitor (IC50 = 0.67 µM in a TRAP assay); selective f… | 10 mg | 24301-10 | More Info |
| MST-312 | A telomerase inhibitor (IC50 = 0.67 µM in a TRAP assay); selective f… | 5 mg | 24301-5 | More Info |
| MSX-122 | A partial antagonist of CXCR4; reduces inflammation in a mouse model of ex… | 1 mg | 23426-1 | More Info |
| MSX-122 | A partial antagonist of CXCR4; reduces inflammation in a mouse model of ex… | 10 mg | 23426-10 | More Info |
| MSX-122 | A partial antagonist of CXCR4; reduces inflammation in a mouse model of ex… | 25 mg | 23426-25 | More Info |
| MSX-122 | A partial antagonist of CXCR4; reduces inflammation in a mouse model of ex… | 5 mg | 23426-5 | More Info |
| MSX-130 | An imidazole; displays excitation / emission maxima of 382 / 466 nm, respe… | 10 mg | 36804-10 | More Info |
| MSX-130 | An imidazole; displays excitation / emission maxima of 382 / 466 nm, respe… | 25 mg | 36804-25 | More Info |
| MSX-130 | An imidazole; displays excitation / emission maxima of 382 / 466 nm, respe… | 5 mg | 36804-5 | More Info |
| MSX-130 | An imidazole; displays excitation / emission maxima of 382 / 466 nm, respe… | 50 mg | 36804-50 | More Info |
| MT-802 | A PROTAC that drives BTK degradation; induces degradation of BTK in NAMALW… | 25 mg | 36581-25 | More Info |
| MT-802 | A PROTAC that drives BTK degradation; induces degradation of BTK in NAMALW… | 5 mg | 36581-5 | More Info |
| MT-802 | A PROTAC that drives BTK degradation; induces degradation of BTK in NAMALW… | 50 mg | 36581-50 | More Info |
| 4-MTA | A methylthio analog of PMA, a hallucinogenic drug that has been scheduled… | 1 mg | 11555-1 | More Info |
| 4-MTA | A methylthio analog of PMA, a hallucinogenic drug that has been scheduled… | 10 mg | 11555-10 | More Info |
| 4-MTA | A methylthio analog of PMA, a hallucinogenic drug that has been scheduled… | 5 mg | 11555-5 | More Info |
| 4-MTA (hydrochloride) | A selective serotonergic agent which increases serotonin release, blocks i… | 1 mg | 11862-1 | More Info |
| 4-MTA (hydrochloride) | A selective serotonergic agent which increases serotonin release, blocks i… | 10 mg | 11862-10 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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Ann Arbor MI 48108
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