CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 645 of 865
Non-Antibody Products
Page 645 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Piriprost (potassium salt) | Piriprost is a structural analog of PGI2 with low IP receptor-mediated act… | 5 mg | 18228-5 | More Info |
| Piriprost (potassium salt) | Piriprost is a structural analog of PGI2 with low IP receptor-mediated act… | 50 mg | 18228-50 | More Info |
| Pirlimycin | A lincosamide antibiotic effective against Gram-positive bacteria that act… | 1 mg | 20138-1 | More Info |
| Pirlimycin | A lincosamide antibiotic effective against Gram-positive bacteria that act… | 5 mg | 20138-5 | More Info |
| Pirlindole | A selective and reversible MAO-A inhibitor (IC50s = 250 and 34.2 nM for ra… | 10 mg | 22060-10 | More Info |
| Pirlindole | A selective and reversible MAO-A inhibitor (IC50s = 250 and 34.2 nM for ra… | 25 mg | 22060-25 | More Info |
| Pirlindole | A selective and reversible MAO-A inhibitor (IC50s = 250 and 34.2 nM for ra… | 5 mg | 22060-5 | More Info |
| Pirlindole | A selective and reversible MAO-A inhibitor (IC50s = 250 and 34.2 nM for ra… | 50 mg | 22060-50 | More Info |
| Pirlindole-d4 (hydrochloride) | An internal standard for the quantification of pirlindole by GC- or LC-MS | 1 mg | 33375-1 | More Info |
| Pirlindole-d4 (hydrochloride) | An internal standard for the quantification of pirlindole by GC- or LC-MS | 500 µg | 33375-500 | More Info |
| Pirmenol | A class I antiarrhythmic agent; lengthens the final repolarization of acti… | 1 mg | 29042-1 | More Info |
| Pirmenol | A class I antiarrhythmic agent; lengthens the final repolarization of acti… | 10 mg | 29042-10 | More Info |
| Pirmenol | A class I antiarrhythmic agent; lengthens the final repolarization of acti… | 25 mg | 29042-25 | More Info |
| Pirmenol | A class I antiarrhythmic agent; lengthens the final repolarization of acti… | 5 mg | 29042-5 | More Info |
| Pirodavir | A broad-spectrum antipicornaviral agent; active against 80 typed (MICs = 0… | 1 mg | 22922-1 | More Info |
| Pirodavir | A broad-spectrum antipicornaviral agent; active against 80 typed (MICs = 0… | 10 mg | 22922-10 | More Info |
| Pirodavir | A broad-spectrum antipicornaviral agent; active against 80 typed (MICs = 0… | 25 mg | 22922-25 | More Info |
| Pirodavir | A broad-spectrum antipicornaviral agent; active against 80 typed (MICs = 0… | 5 mg | 22922-5 | More Info |
| Piromidic Acid | A quinolone antibiotic; active against Gram-positive and Gram-negative bac… | 1 g | 19255-1 | More Info |
| Piromidic Acid | A quinolone antibiotic; active against Gram-positive and Gram-negative bac… | 100 mg | 19255-100 | More Info |
| Piromidic Acid | A quinolone antibiotic; active against Gram-positive and Gram-negative bac… | 500 mg | 19255-500 | More Info |
| Pironetin | A bacterial metabolite; binds to tubulin (Kd = 0.33 µM); increases t… | 1 mg | 28853-1 | More Info |
| Piroxicam | A COX inhibitor and NSAID; inhibits TXB2 production from arachidonic acid… | 1 g | 13368-1 | More Info |
| Piroxicam | A COX inhibitor and NSAID; inhibits TXB2 production from arachidonic acid… | 10 g | 13368-10 | More Info |
| Piroxicam | A COX inhibitor and NSAID; inhibits TXB2 production from arachidonic acid… | 5 g | 13368-5 | More Info |
| Piroxicam | A COX inhibitor and NSAID; inhibits TXB2 production from arachidonic acid… | 500 mg | 13368-500 | More Info |
| Piroxicam-d3 | An internal standard for the quantification of piroxicam by GC- or LC-MS | 1 mg | 33248-1 | More Info |
| Piroxicam-d3 | An internal standard for the quantification of piroxicam by GC- or LC-MS | 5 mg | 33248-5 | More Info |
| Pirozadil | A lipid-lowering agent; reduces serum and aortic cholesterol levels, serum… | 100 mg | 37292-100 | More Info |
| Pirozadil | A lipid-lowering agent; reduces serum and aortic cholesterol levels, serum… | 25 mg | 37292-25 | More Info |
| Pirozadil | A lipid-lowering agent; reduces serum and aortic cholesterol levels, serum… | 250 mg | 37292-250 | More Info |
| Pirozadil | A lipid-lowering agent; reduces serum and aortic cholesterol levels, serum… | 50 mg | 37292-50 | More Info |
| Pirtobrutinib | A BTK inhibitor (IC50s = 10-100 and C481S, respectively); selective for BT… | 10 mg | 36775-10 | More Info |
| Pirtobrutinib | A BTK inhibitor (IC50s = 10-100 and C481S, respectively); selective for BT… | 25 mg | 36775-25 | More Info |
| Pirtobrutinib | A BTK inhibitor (IC50s = 10-100 and C481S, respectively); selective for BT… | 5 mg | 36775-5 | More Info |
| Pirtobrutinib | A BTK inhibitor (IC50s = 10-100 and C481S, respectively); selective for BT… | 50 mg | 36775-50 | More Info |
| PIT-1 | A selective nonphosphoinositide inhibitor that specifically disrupts PIP3… | 10 mg | 10728-10 | More Info |
| PIT-1 | A selective nonphosphoinositide inhibitor that specifically disrupts PIP3… | 100 mg | 10728-100 | More Info |
| PIT-1 | A selective nonphosphoinositide inhibitor that specifically disrupts PIP3… | 5 mg | 10728-5 | More Info |
| PIT-1 | A selective nonphosphoinositide inhibitor that specifically disrupts PIP3… | 50 mg | 10728-50 | More Info |
| Pitavastatin (calcium salt) | An HMG-CoA reductase inhibitor (Ki = 1.7 nM for the rat liver microsomal e… | 10 mg | 15414-10 | More Info |
| Pitavastatin (calcium salt) | An HMG-CoA reductase inhibitor (Ki = 1.7 nM for the rat liver microsomal e… | 100 mg | 15414-100 | More Info |
| Pitavastatin (calcium salt) | An HMG-CoA reductase inhibitor (Ki = 1.7 nM for the rat liver microsomal e… | 25 mg | 15414-25 | More Info |
| Pitavastatin (calcium salt) | An HMG-CoA reductase inhibitor (Ki = 1.7 nM for the rat liver microsomal e… | 50 mg | 15414-50 | More Info |
| Pitavastatin lactone | A major phase 2 metabolite of pitavastatin; formed when pitavastatin under… | 1 mg | 21785-1 | More Info |
| Pitavastatin lactone | A major phase 2 metabolite of pitavastatin; formed when pitavastatin under… | 5 mg | 21785-5 | More Info |
| Pitavastatin lactone | A major phase 2 metabolite of pitavastatin; formed when pitavastatin under… | 500 µg | 21785-500 | More Info |
| Pitavastatin lactone-d4 | An internal standard for the quantification of pitavastatin lactone by GC-… | 1 mg | 34696-1 | More Info |
| Pitavastatin lactone-d4 | An internal standard for the quantification of pitavastatin lactone by GC-… | 5 mg | 34696-5 | More Info |
| Pitavastatin lactone-d4 | An internal standard for the quantification of pitavastatin lactone by GC-… | 500 µg | 34696-500 | More Info |
| Pitofenone (hydrochloride) | An antispasmodic agent; an inhibitor of AChE (Kis = 36 and 45 µM for… | 10 mg | 23865-10 | More Info |
| Pitofenone (hydrochloride) | An antispasmodic agent; an inhibitor of AChE (Kis = 36 and 45 µM for… | 25 mg | 23865-25 | More Info |
| Pitofenone (hydrochloride) | An antispasmodic agent; an inhibitor of AChE (Kis = 36 and 45 µM for… | 5 mg | 23865-5 | More Info |
| Pitofenone (hydrochloride) | An antispasmodic agent; an inhibitor of AChE (Kis = 36 and 45 µM for… | 50 mg | 23865-50 | More Info |
| Pitolisant | A histamine H3 receptor antagonist (Ki = 0.16 nM) and inverse agonist (EC5… | 1 mg | 19307-1 | More Info |
| Pitolisant | A histamine H3 receptor antagonist (Ki = 0.16 nM) and inverse agonist (EC5… | 10 mg | 19307-10 | More Info |
| Pitolisant | A histamine H3 receptor antagonist (Ki = 0.16 nM) and inverse agonist (EC5… | 5 mg | 19307-5 | More Info |
| Pitolisant | A histamine H3 receptor antagonist (Ki = 0.16 nM) and inverse agonist (EC5… | 50 mg | 19307-50 | More Info |
| Pitstop2 | An inhibitor of the amphiphysin-clathrin interaction (IC50 = 12 µM);… | 1 mg | 23885-1 | More Info |
| Pitstop2 | An inhibitor of the amphiphysin-clathrin interaction (IC50 = 12 µM);… | 10 mg | 23885-10 | More Info |
| Pitstop2 | An inhibitor of the amphiphysin-clathrin interaction (IC50 = 12 µM);… | 5 mg | 23885-5 | More Info |
| Pivaloyl fentanyl (hydrochloride) | An analytical reference standard categorized as an opioid; regulated as a… | 1 mg | 22991-1 | More Info |
| Pivaloyl fentanyl (hydrochloride) | An analytical reference standard categorized as an opioid; regulated as a… | 5 mg | 22991-5 | More Info |
| Pixantrone-d8 (maleate) | An internal standard for the quantification of pixantrone by GC- or LC-MS | 1 mg | 33292-1 | More Info |
| Pixantrone-d8 (maleate) | An internal standard for the quantification of pixantrone by GC- or LC-MS | 5 mg | 33292-5 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 1 mg | 20055-1 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 10 mg | 20055-10 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 25 mg | 20055-25 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 5 mg | 20055-5 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 1 g | 20765-1 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 100 mg | 20765-100 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 250 mg | 20765-250 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 500 mg | 20765-500 | More Info |
| PJ-34 (hydrochloride) | An inhibitor of PARPs which can be used in cells or in animals; binds and… | 1 mg | 14440-1 | More Info |
| PJ-34 (hydrochloride) | An inhibitor of PARPs which can be used in cells or in animals; binds and… | 10 mg | 14440-10 | 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)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
Sales: sales@caymanchem.com
http://www.caymanchem.com
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