ALOMONE LABS Non-Antibody Products — page 47 of 47
Non-Antibody Products
Page 47 of 47
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| WS 12 | WS 12 is a TRPM8 channel activator (EC50 = 193 nM)1. Synthetic. Purity >99… | 10 mg | W-105 | More Info |
| WS 12 | WS 12 is a TRPM8 channel activator (EC50 = 193 nM)1. Synthetic. Purity >99… | 25 mg | W-105 | More Info |
| WS 12 | WS 12 is a TRPM8 channel activator (EC50 = 193 nM)1. Synthetic. Purity >99… | 5 mg | W-105 | More Info |
| WS 12 | WS 12 is a TRPM8 channel activator (EC50 = 193 nM)1. Synthetic. Purity >99… | 50 mg | W-105 | More Info |
| WS 3 | WS 3 is a TRPM8 channel activator (EC50 = 3.7 µM)1. Synthetic. Purit… | 1 g | W-100 | More Info |
| WS 3 | WS 3 is a TRPM8 channel activator (EC50 = 3.7 µM)1. Synthetic. Purit… | 10 g | W-100 | More Info |
| WS 3 | WS 3 is a TRPM8 channel activator (EC50 = 3.7 µM)1. Synthetic. Purit… | 5 g | W-100 | More Info |
| XE991 | A Blocker of KCNQ Channels. Synthetic. Purity >95%. MW: 376.45 | 10 mg | X-100 | More Info |
| XE991 | A Blocker of KCNQ Channels. Synthetic. Purity >95%. MW: 376.45 | 25 mg | X-100 | More Info |
| XE991 | A Blocker of KCNQ Channels. Synthetic. Purity >95%. MW: 376.45 | 5 mg | X-100 | More Info |
| XE991 | A Blocker of KCNQ Channels. Synthetic. Purity >95%. MW: 376.45 | 50 mg | X-100 | More Info |
| XE991 dihydrochloride | XE991 blocks KCNQ channels with IC50 of 0.5-10 µM1. Synthetic. Purit… | 10 mg | X-101 | More Info |
| XE991 dihydrochloride | XE991 blocks KCNQ channels with IC50 of 0.5-10 µM1. Synthetic. Purit… | 25 mg | X-101 | More Info |
| XE991 dihydrochloride | XE991 blocks KCNQ channels with IC50 of 0.5-10 µM1. Synthetic. Purit… | 5 mg | X-101 | More Info |
| XE991 dihydrochloride | XE991 blocks KCNQ channels with IC50 of 0.5-10 µM1. Synthetic. Purit… | 50 mg | X-101 | More Info |
| XEN907 | XEN907 is a NaV1.7 channel blocker with an IC50 value of 5 nM for the chan… | 10 mg | X-105 | More Info |
| XEN907 | XEN907 is a NaV1.7 channel blocker with an IC50 value of 5 nM for the chan… | 25 mg | X-105 | More Info |
| XEN907 | XEN907 is a NaV1.7 channel blocker with an IC50 value of 5 nM for the chan… | 5 mg | X-105 | More Info |
| [Y]6-Angiotensin II Analog | Y6-Angiotensin Analog is an AT2R agonist1,2. Synthetic peptide. Purity &ge… | 0.1 mg | SPA-175 | More Info |
| [Y]6-Angiotensin II Analog | Y6-Angiotensin Analog is an AT2R agonist1,2. Synthetic peptide. Purity &ge… | 0.5 mg | SPA-175 | More Info |
| [Y]6-Angiotensin II Analog | Y6-Angiotensin Analog is an AT2R agonist1,2. Synthetic peptide. Purity &ge… | 1 mg | SPA-175 | More Info |
| [Y]6-Angiotensin II Analog | Y6-Angiotensin Analog is an AT2R agonist1,2. Synthetic peptide. Purity &ge… | 10 mg | SPA-175 | More Info |
| [Y]6-Angiotensin II Analog | Y6-Angiotensin Analog is an AT2R agonist1,2. Synthetic peptide. Purity &ge… | 5 mg | SPA-175 | More Info |
| YM 90K hydrochloride | YM 90K hydrochloride is a selective AMPA receptor antagonist; Ki of 84 nM1… | 10 mg | Y-105 | More Info |
| YM 90K hydrochloride | YM 90K hydrochloride is a selective AMPA receptor antagonist; Ki of 84 nM1… | 25 mg | Y-105 | More Info |
| YM 90K hydrochloride | YM 90K hydrochloride is a selective AMPA receptor antagonist; Ki of 84 nM1… | 5 mg | Y-105 | More Info |
| YM 90K hydrochloride | YM 90K hydrochloride is a selective AMPA receptor antagonist; Ki of 84 nM1… | 50 mg | Y-105 | More Info |
| Zacopride hydrochloride | Zacopride hydrochloride is a highly potent 5-HT3 receptor antagonist (Ki =… | 10 mg | Z-110 | More Info |
| Zacopride hydrochloride | Zacopride hydrochloride is a highly potent 5-HT3 receptor antagonist (Ki =… | 25 mg | Z-110 | More Info |
| Zacopride hydrochloride | Zacopride hydrochloride is a highly potent 5-HT3 receptor antagonist (Ki =… | 5 mg | Z-110 | More Info |
| Zacopride hydrochloride | Zacopride hydrochloride is a highly potent 5-HT3 receptor antagonist (Ki =… | 50 mg | Z-110 | More Info |
| Zaleplon | A non-benzodiazepine pyrazolopyrimidine agonist at the benzodiazepine site… | 10 mg | Z-140 | More Info |
| Zaleplon | A non-benzodiazepine pyrazolopyrimidine agonist at the benzodiazepine site… | 100 mg | Z-140 | More Info |
| Zaleplon | A non-benzodiazepine pyrazolopyrimidine agonist at the benzodiazepine site… | 25 mg | Z-140 | More Info |
| Zaleplon | A non-benzodiazepine pyrazolopyrimidine agonist at the benzodiazepine site… | 50 mg | Z-140 | More Info |
| ZD 9379 | ZD 9379 is a NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 383.79 | 10 mg | Z-120 | More Info |
| ZD 9379 | ZD 9379 is a NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 383.79 | 25 mg | Z-120 | More Info |
| ZD 9379 | ZD 9379 is a NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 383.79 | 5 mg | Z-120 | More Info |
| Zibotentan | Zibotentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 10 mg | Z-130 | More Info |
| Zibotentan | Zibotentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 100 mg | Z-130 | More Info |
| Zibotentan | Zibotentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 25 mg | Z-130 | More Info |
| Zibotentan | Zibotentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 5 mg | Z-130 | More Info |
| Zibotentan | Zibotentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 50 mg | Z-130 | More Info |
| ZINC58368839 | ZINC58368839 is a novel antagonist of purinergic P2X7 receptors, shown to… | 10 mg | Z-135 | More Info |
| ZINC58368839 | ZINC58368839 is a novel antagonist of purinergic P2X7 receptors, shown to… | 25 mg | Z-135 | More Info |
| ZINC58368839 | ZINC58368839 is a novel antagonist of purinergic P2X7 receptors, shown to… | 5 mg | Z-135 | More Info |
| ZINC58368839 | ZINC58368839 is a novel antagonist of purinergic P2X7 receptors, shown to… | 50 mg | Z-135 | More Info |
| ZINC9315614 | ZINC9315614 is a novel antagonist of the purinergic P2X7 receptors, shown… | 10 mg | Z-145 | More Info |
| ZINC9315614 | ZINC9315614 is a novel antagonist of the purinergic P2X7 receptors, shown… | 25 mg | Z-145 | More Info |
| ZINC9315614 | ZINC9315614 is a novel antagonist of the purinergic P2X7 receptors, shown… | 5 mg | Z-145 | More Info |
| ZINC9315614 | ZINC9315614 is a novel antagonist of the purinergic P2X7 receptors, shown… | 50 mg | Z-145 | More Info |
| Zolpidem | GABA(A) receptor agonist at the benzodiazepine site, potent and highly sel… | 10 mg | Z-100 | More Info |
| Zolpidem | GABA(A) receptor agonist at the benzodiazepine site, potent and highly sel… | 25 mg | Z-100 | More Info |
| Zolpidem | GABA(A) receptor agonist at the benzodiazepine site, potent and highly sel… | 5 mg | Z-100 | More Info |
| Zolpidem | GABA(A) receptor agonist at the benzodiazepine site, potent and highly sel… | 50 mg | Z-100 | More Info |
ALOMONE LABS
ALOMONE LABS
Jerusalem BioPark (JBP), Hadassah Ein Kerem
PO Box 4287
Jerusalem, 9104201 ISRAEL
P: +972-2-587-2202
F: +972-2-587-1101
info@alomone.com
http://www.alomone.com
U.S.A. OFFICE
Toll free phone: 1800-618-1644 / 1800-791-3904
Toll free fax: 1888-454-7276 / 1800-791-3912
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