CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 428 of 1
Non-Antibody Products
Page 428 of 1,297
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| E3 Ligand-Linker Conjugate 3 | A PROTAC building block containing thalidomide; has been used in the synth… | 25 mg | 36666-25 | More Info |
| E3 Ligand-Linker Conjugate 3 | A PROTAC building block containing thalidomide; has been used in the synth… | 5 mg | 36666-5 | More Info |
| E3 Ligand-Linker Conjugate 3 | A PROTAC building block containing thalidomide; has been used in the synth… | 50 mg | 36666-50 | More Info |
| E3 Ligase Ligand 2 | An active metabolite of thalidomide and a PROTAC synthetic intermediate; d… | 1 g | 36664-1 | More Info |
| E3 Ligase Ligand 2 | An active metabolite of thalidomide and a PROTAC synthetic intermediate; d… | 5 g | 36664-5 | More Info |
| Eliglustat-d15 (tartrate) | An internal standard for the quantification of eliglustat by GC- or LC-MS | 1 mg | 30167-1 | More Info |
| Eliglustat-d15 (tartrate) | An internal standard for the quantification of eliglustat by GC- or LC-MS | 5 mg | 30167-5 | More Info |
| Eliglustat (hemitartrate) | A glucosylceramide synthase inhibitor (IC50 = 40 nM for inhibition of gluc… | 1 mg | 21487-1 | More Info |
| Eliglustat (hemitartrate) | A glucosylceramide synthase inhibitor (IC50 = 40 nM for inhibition of gluc… | 10 mg | 21487-10 | More Info |
| Eliglustat (hemitartrate) | A glucosylceramide synthase inhibitor (IC50 = 40 nM for inhibition of gluc… | 25 mg | 21487-25 | More Info |
| Eliglustat (hemitartrate) | A glucosylceramide synthase inhibitor (IC50 = 40 nM for inhibition of gluc… | 5 mg | 21487-5 | More Info |
| Elinogrel | A reversible antagonist of P2Y12 (Ki = 23 nM); inhibits platelet aggregati… | 1 mg | 25976-1 | More Info |
| Elinogrel | A reversible antagonist of P2Y12 (Ki = 23 nM); inhibits platelet aggregati… | 5 mg | 25976-5 | More Info |
| Eliprodil | A non-competitive NMDA receptor antagonist that inhibits neuronal calcium… | 10 mg | 18398-10 | More Info |
| Eliprodil | A non-competitive NMDA receptor antagonist that inhibits neuronal calcium… | 5 mg | 18398-5 | More Info |
| Eliprodil | A non-competitive NMDA receptor antagonist that inhibits neuronal calcium… | 50 mg | 18398-50 | More Info |
| Ellagic Acid | A polyphenolic antioxidant that is abundant in many fruits, vegetables, pl… | 1 g | 10569-1 | More Info |
| Ellagic Acid | A polyphenolic antioxidant that is abundant in many fruits, vegetables, pl… | 100 mg | 10569-100 | More Info |
| Ellagic Acid | A polyphenolic antioxidant that is abundant in many fruits, vegetables, pl… | 500 mg | 10569-500 | More Info |
| Ellipticine (hydrochloride) | A DNA-intercalating antitumor agent that forms covalent adducts in DNA aft… | 10 mg | 18742-10 | More Info |
| Ellipticine (hydrochloride) | A DNA-intercalating antitumor agent that forms covalent adducts in DNA aft… | 25 mg | 18742-25 | More Info |
| Ellipticine (hydrochloride) | A DNA-intercalating antitumor agent that forms covalent adducts in DNA aft… | 5 mg | 18742-5 | More Info |
| Ellipticine (hydrochloride) | A DNA-intercalating antitumor agent that forms covalent adducts in DNA aft… | 50 mg | 18742-50 | More Info |
| ELN484228 | An inhibitor of α-synuclein-induced toxicity; prevents inhibition of… | 10 mg | 29398-10 | More Info |
| ELN484228 | An inhibitor of α-synuclein-induced toxicity; prevents inhibition of… | 100 mg | 29398-100 | More Info |
| ELN484228 | An inhibitor of α-synuclein-induced toxicity; prevents inhibition of… | 5 mg | 29398-5 | More Info |
| ELN484228 | An inhibitor of α-synuclein-induced toxicity; prevents inhibition of… | 50 mg | 29398-50 | More Info |
| Elobixibat | An inhibitor of ASBT (IC50s = 0.53, 0.13, and 5.8 nM for the human, mouse,… | 1 mg | 30658-1 | More Info |
| Elobixibat | An inhibitor of ASBT (IC50s = 0.53, 0.13, and 5.8 nM for the human, mouse,… | 10 mg | 30658-10 | More Info |
| Elobixibat | An inhibitor of ASBT (IC50s = 0.53, 0.13, and 5.8 nM for the human, mouse,… | 25 mg | 30658-25 | More Info |
| Elobixibat | An inhibitor of ASBT (IC50s = 0.53, 0.13, and 5.8 nM for the human, mouse,… | 5 mg | 30658-5 | More Info |
| ELOVL1-22 | An inhibitor of ELOVL1; inhibits LPC(C26:0) synthesis in HEK293 cells (IC5… | 1 mg | 36142-1 | More Info |
| ELOVL1-22 | An inhibitor of ELOVL1; inhibits LPC(C26:0) synthesis in HEK293 cells (IC5… | 10 mg | 36142-10 | More Info |
| ELOVL1-22 | An inhibitor of ELOVL1; inhibits LPC(C26:0) synthesis in HEK293 cells (IC5… | 25 mg | 36142-25 | More Info |
| ELOVL1-22 | An inhibitor of ELOVL1; inhibits LPC(C26:0) synthesis in HEK293 cells (IC5… | 5 mg | 36142-5 | More Info |
| ELOVL1-27 | An inhibitor of ELOVL1 (IC50 = 900 nM); inhibits LPC(C26:0) synthesis in H… | 1 mg | 35323-1 | More Info |
| ELOVL1-27 | An inhibitor of ELOVL1 (IC50 = 900 nM); inhibits LPC(C26:0) synthesis in H… | 10 mg | 35323-10 | More Info |
| ELOVL1-27 | An inhibitor of ELOVL1 (IC50 = 900 nM); inhibits LPC(C26:0) synthesis in H… | 25 mg | 35323-25 | More Info |
| ELOVL1-27 | An inhibitor of ELOVL1 (IC50 = 900 nM); inhibits LPC(C26:0) synthesis in H… | 5 mg | 35323-5 | More Info |
| ELR510444 | An inhibitor of tubulin polymerization (IC50 = 10 µM); binds to tubu… | 1 mg | 17696-1 | More Info |
| ELR510444 | An inhibitor of tubulin polymerization (IC50 = 10 µM); binds to tubu… | 10 mg | 17696-10 | More Info |
| ELR510444 | An inhibitor of tubulin polymerization (IC50 = 10 µM); binds to tubu… | 25 mg | 17696-25 | More Info |
| ELR510444 | An inhibitor of tubulin polymerization (IC50 = 10 µM); binds to tubu… | 5 mg | 17696-5 | More Info |
| Elsinochrome A | A perylenequinone fungal metabolite; induces the production of singlet oxy… | 1 mg | 33072-1 | More Info |
| Elsinochrome A | A perylenequinone fungal metabolite; induces the production of singlet oxy… | 5 mg | 33072-5 | More Info |
| Eltenac | A non-selective COX inhibitor (IC50 = 0.03 µM for both COX-1 and COX… | 1 mg | 27673-1 | More Info |
| Eltenac | A non-selective COX inhibitor (IC50 = 0.03 µM for both COX-1 and COX… | 5 mg | 27673-5 | More Info |
| Eltenac | A non-selective COX inhibitor (IC50 = 0.03 µM for both COX-1 and COX… | 500 µg | 27673-500 | More Info |
| Eltoprazine (hydrochloride) | A partial agonist at 5-HT1A, 5-HT1B, and 5-HT2B receptors (Kis = 40, 52, a… | 1 mg | 18428-1 | More Info |
| Eltoprazine (hydrochloride) | A partial agonist at 5-HT1A, 5-HT1B, and 5-HT2B receptors (Kis = 40, 52, a… | 10 mg | 18428-10 | 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
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http://www.caymanchem.com
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