CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 642 of 865
Non-Antibody Products
Page 642 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Pimavanserin | A 5-HT2A inverse agonist (IC50 = 1.86 nM; Ki = 0.5 nM); selective for 5-HT… | 10 mg | 23462-10 | More Info |
| Pimavanserin | A 5-HT2A inverse agonist (IC50 = 1.86 nM; Ki = 0.5 nM); selective for 5-HT… | 25 mg | 23462-25 | More Info |
| Pimavanserin | A 5-HT2A inverse agonist (IC50 = 1.86 nM; Ki = 0.5 nM); selective for 5-HT… | 5 mg | 23462-5 | More Info |
| Pimavanserin | A 5-HT2A inverse agonist (IC50 = 1.86 nM; Ki = 0.5 nM); selective for 5-HT… | 50 mg | 23462-50 | More Info |
| Pimecrolimus | A macrolactam that binds to macrophilin-12 and inhibits calcineurin as wel… | 10 mg | 13107-10 | More Info |
| Pimecrolimus | A macrolactam that binds to macrophilin-12 and inhibits calcineurin as wel… | 100 mg | 13107-100 | More Info |
| Pimecrolimus | A macrolactam that binds to macrophilin-12 and inhibits calcineurin as wel… | 50 mg | 13107-50 | More Info |
| Pimelic Diphenylamide 106 | A slow, tight-binding inhibitor of class I HDACs, progressively binding HD… | 1 mg | 13212-1 | More Info |
| Pimelic Diphenylamide 106 | A slow, tight-binding inhibitor of class I HDACs, progressively binding HD… | 10 mg | 13212-10 | More Info |
| Pimelic Diphenylamide 106 | A slow, tight-binding inhibitor of class I HDACs, progressively binding HD… | 25 mg | 13212-25 | More Info |
| Pimelic Diphenylamide 106 | A slow, tight-binding inhibitor of class I HDACs, progressively binding HD… | 5 mg | 13212-5 | More Info |
| Pim-1 Inhibitor 2 | A potent Pim-1 inhibitor (Ki = 91 nM) that targets the ATP-binding kinase… | 1 mg | 17809-1 | More Info |
| Pim-1 Inhibitor 2 | A potent Pim-1 inhibitor (Ki = 91 nM) that targets the ATP-binding kinase… | 10 mg | 17809-10 | More Info |
| Pim-1 Inhibitor 2 | A potent Pim-1 inhibitor (Ki = 91 nM) that targets the ATP-binding kinase… | 5 mg | 17809-5 | More Info |
| Pimobendan | An inhibitor of PDE3 (IC50 = 0.32 µM for guinea pig cardiac enzyme);… | 100 mg | 26082-100 | More Info |
| Pimobendan | An inhibitor of PDE3 (IC50 = 0.32 µM for guinea pig cardiac enzyme);… | 25 mg | 26082-25 | More Info |
| Pimobendan | An inhibitor of PDE3 (IC50 = 0.32 µM for guinea pig cardiac enzyme);… | 50 mg | 26082-50 | More Info |
| Pimodivir | An inhibitor of influenza virus PB2 (KD = ~1.6 µM) and inhibits the… | 10 mg | 29321-10 | More Info |
| Pimodivir | An inhibitor of influenza virus PB2 (KD = ~1.6 µM) and inhibits the… | 25 mg | 29321-25 | More Info |
| Pimodivir | An inhibitor of influenza virus PB2 (KD = ~1.6 µM) and inhibits the… | 5 mg | 29321-5 | More Info |
| Pimonidazole | A small molecule radiosensitizer that has proven to be an effective and no… | 10 mg | 89130-10 | More Info |
| Pimonidazole | A small molecule radiosensitizer that has proven to be an effective and no… | 100 mg | 89130-100 | More Info |
| Pimonidazole | A small molecule radiosensitizer that has proven to be an effective and no… | 5 mg | 89130-5 | More Info |
| Pimonidazole | A small molecule radiosensitizer that has proven to be an effective and no… | 50 mg | 89130-50 | More Info |
| Pimozide | A dopamine receptor antagonist (Kis = 2.4, 0.3, and 1.8 nM for D2, D3, and… | 100 mg | 16222-100 | More Info |
| Pimozide | A dopamine receptor antagonist (Kis = 2.4, 0.3, and 1.8 nM for D2, D3, and… | 250 mg | 16222-250 | More Info |
| Pimozide | A dopamine receptor antagonist (Kis = 2.4, 0.3, and 1.8 nM for D2, D3, and… | 50 mg | 16222-50 | More Info |
| Pimozide-d4 | An internal standard for the quantification of pimozide by GC- or LC-MS, | 1 mg | 28617-1 | More Info |
| Pimpinellin | A coumarin derivative with diverse biological activities; inhibits AChE an… | 10 mg | 36274-10 | More Info |
| Pimpinellin | A coumarin derivative with diverse biological activities; inhibits AChE an… | 25 mg | 36274-25 | More Info |
| Pimpinellin | A coumarin derivative with diverse biological activities; inhibits AChE an… | 5 mg | 36274-5 | More Info |
| Pimpinellin | A coumarin derivative with diverse biological activities; inhibits AChE an… | 50 mg | 36274-50 | More Info |
| Pimprinine | An alkaloid with diverse biological activities; inhibits deamination of 5-… | 1 mg | 25507-1 | More Info |
| Pimprinine | An alkaloid with diverse biological activities; inhibits deamination of 5-… | 5 mg | 25507-5 | More Info |
| Pinacidil (hydrate) | A potassium channel opener, activating the ATP-modulated potassium channel… | 100 mg | 15416-100 | More Info |
| Pinacidil (hydrate) | A potassium channel opener, activating the ATP-modulated potassium channel… | 25 mg | 15416-25 | More Info |
| Pinacidil (hydrate) | A potassium channel opener, activating the ATP-modulated potassium channel… | 250 mg | 15416-250 | More Info |
| Pinacidil (hydrate) | A potassium channel opener, activating the ATP-modulated potassium channel… | 50 mg | 15416-50 | More Info |
| Pinane Thromboxane A2 | PTA2 is a stable analog of TXA2. It is a TP receptor antagonist and an inh… | 1 mg | 19020-1 | More Info |
| Pinane Thromboxane A2 | PTA2 is a stable analog of TXA2. It is a TP receptor antagonist and an inh… | 10 mg | 19020-10 | More Info |
| Pinane Thromboxane A2 | PTA2 is a stable analog of TXA2. It is a TP receptor antagonist and an inh… | 5 mg | 19020-5 | More Info |
| Pinane Thromboxane A2 | PTA2 is a stable analog of TXA2. It is a TP receptor antagonist and an inh… | 500 µg | 19020-500 | More Info |
| Pinaverium (bromide) | An L-type calcium channel inhibitor (IC50 = 1.5 µM in a patch-clamp… | 1 mg | 40653-1 | More Info |
| Pinaverium (bromide) | An L-type calcium channel inhibitor (IC50 = 1.5 µM in a patch-clamp… | 10 mg | 40653-10 | More Info |
| Pinaverium (bromide) | An L-type calcium channel inhibitor (IC50 = 1.5 µM in a patch-clamp… | 25 mg | 40653-25 | More Info |
| Pinaverium (bromide) | An L-type calcium channel inhibitor (IC50 = 1.5 µM in a patch-clamp… | 5 mg | 40653-5 | More Info |
| Pindolol | A β1- and β2-AR antagonist (Kis = 2.6 and 4.8 nM, respectively);… | 100 mg | 21445-100 | More Info |
| Pindolol | A β1- and β2-AR antagonist (Kis = 2.6 and 4.8 nM, respectively);… | 250 mg | 21445-250 | More Info |
| Pindolol | A β1- and β2-AR antagonist (Kis = 2.6 and 4.8 nM, respectively);… | 50 mg | 21445-50 | More Info |
| Pindolol | A β1- and β2-AR antagonist (Kis = 2.6 and 4.8 nM, respectively);… | 500 mg | 21445-500 | More Info |
| PINK1 Blocking Peptide | Peptide Sequence: human PINK1 amino acids 484-504 · To be used in c… | 1 ea | 10006284-1 | More Info |
| Pinocembrin | A flavonoid with diverse biological activities; induces apoptosis in, and… | 10 mg | 29852-10 | More Info |
| Pinocembrin | A flavonoid with diverse biological activities; induces apoptosis in, and… | 100 mg | 29852-100 | More Info |
| Pinocembrin | A flavonoid with diverse biological activities; induces apoptosis in, and… | 250 mg | 29852-250 | More Info |
| Pinocembrin | A flavonoid with diverse biological activities; induces apoptosis in, and… | 50 mg | 29852-50 | More Info |
| Pinolenic Acid | Pinolenic acid is a PUFA found in Korean pine (Pinus orientalis) and marit… | 10 mg | 10008654-10 | More Info |
| Pinolenic Acid | Pinolenic acid is a PUFA found in Korean pine (Pinus orientalis) and marit… | 100 mg | 10008654-100 | More Info |
| Pinolenic Acid | Pinolenic acid is a PUFA found in Korean pine (Pinus orientalis) and marit… | 25 mg | 10008654-25 | More Info |
| Pinolenic Acid | Pinolenic acid is a PUFA found in Korean pine (Pinus orientalis) and marit… | 50 mg | 10008654-50 | More Info |
| Pinolenic Acid ethyl ester | Pinolenic acid ethyl ester is a neutral, more lipophilic form of the free… | 10 mg | 10008658-10 | More Info |
| Pinolenic Acid ethyl ester | Pinolenic acid ethyl ester is a neutral, more lipophilic form of the free… | 5 mg | 10008658-5 | More Info |
| Pinolenic Acid ethyl ester | Pinolenic acid ethyl ester is a neutral, more lipophilic form of the free… | 50 mg | 10008658-50 | More Info |
| Pinolenic Acid methyl ester | Pinolenic acid methyl ester is a neutral, more lipophilic form of the free… | 1 mg | 10008656-1 | More Info |
| Pinolenic Acid methyl ester | Pinolenic acid methyl ester is a neutral, more lipophilic form of the free… | 10 mg | 10008656-10 | More Info |
| Pinolenic Acid methyl ester | Pinolenic acid methyl ester is a neutral, more lipophilic form of the free… | 5 mg | 10008656-5 | More Info |
| Pinolenic Acid methyl ester | Pinolenic acid methyl ester is a neutral, more lipophilic form of the free… | 50 mg | 10008656-50 | More Info |
| (+)-Pinoresinol | A lignan with diverse biological activities; an inhibitor of α-gluco… | 10 mg | 27700-10 | More Info |
| (+)-Pinoresinol | A lignan with diverse biological activities; an inhibitor of α-gluco… | 25 mg | 27700-25 | More Info |
| (+)-Pinoresinol | A lignan with diverse biological activities; an inhibitor of α-gluco… | 5 mg | 27700-5 | More Info |
| Pinoresinol Diglucoside | A lignan with diverse biological activities; inhibits peroxidation of a li… | 10 mg | 27708-10 | More Info |
| Pinoresinol Diglucoside | A lignan with diverse biological activities; inhibits peroxidation of a li… | 25 mg | 27708-25 | More Info |
| Pinoresinol Diglucoside | A lignan with diverse biological activities; inhibits peroxidation of a li… | 5 mg | 27708-5 | More Info |
| Pinoresinol Diglucoside | A lignan with diverse biological activities; inhibits peroxidation of a li… | 50 mg | 27708-50 | More Info |
| Pinostilbene | A stable, monomethoxylated resveratrol derivative that at 0.1-10 µM… | 1 mg | 14044-1 | More Info |
| Pinostilbene | A stable, monomethoxylated resveratrol derivative that at 0.1-10 µM… | 10 mg | 14044-10 | 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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