ALOMONE LABS Non-Antibody Products — page 35 of 36
Non-Antibody Products
Page 35 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Verruculogen | Verruculogen is a selective blocker of KCa1.1 (BK) channel. It belongs to… | 1 mg | V-500 | More Info |
| Verruculogen | Verruculogen is a selective blocker of KCa1.1 (BK) channel. It belongs to… | 5 mg | V-500 | More Info |
| VSTX3 | VSTX3 inhibits voltage-gated Na+ channels NaV1.3, NaV1.7 and NaV1.81. Synt… | 0.1 mg | STT-350 | More Info |
| VSTX3 | VSTX3 inhibits voltage-gated Na+ channels NaV1.3, NaV1.7 and NaV1.81. Synt… | 0.5 mg | STT-350 | More Info |
| VSTX3 | VSTX3 inhibits voltage-gated Na+ channels NaV1.3, NaV1.7 and NaV1.81. Synt… | 1 mg | STT-350 | More Info |
| VSTX3 | VSTX3 inhibits voltage-gated Na+ channels NaV1.3, NaV1.7 and NaV1.81. Synt… | 10 mg | STT-350 | More Info |
| VSTX3 | VSTX3 inhibits voltage-gated Na+ channels NaV1.3, NaV1.7 and NaV1.81. Synt… | 5 mg | STT-350 | More Info |
| VSTX3 | VSTX3 inhibits voltage-gated Na+ channels NaV1.3, NaV1.7 and NaV1.81. Synt… | 50 µg | STT-350 | More Info |
| VU0529331 | VU0529331 is a novel activator of homomeric and of non-GIRK1-containing G-… | 10 mg | V-155 | More Info |
| VU0529331 | VU0529331 is a novel activator of homomeric and of non-GIRK1-containing G-… | 25 mg | V-155 | More Info |
| VU0529331 | VU0529331 is a novel activator of homomeric and of non-GIRK1-containing G-… | 5 mg | V-155 | More Info |
| VU0529331 | VU0529331 is a novel activator of homomeric and of non-GIRK1-containing G-… | 50 mg | V-155 | More Info |
| VU591 | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥99%. MW: 368.3 | 10 mg | V-125 | More Info |
| VU591 | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥99%. MW: 368.3 | 25 mg | V-125 | More Info |
| VU591 | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥99%. MW: 368.3 | 5 mg | V-125 | More Info |
| VU590 dihydrochloride | VU590 inhibits ROMK1 channels in a dose-dependent manner with an IC50 of 2… | 10 mg | V-130 | More Info |
| VU590 dihydrochloride | VU590 inhibits ROMK1 channels in a dose-dependent manner with an IC50 of 2… | 25 mg | V-130 | More Info |
| VU590 dihydrochloride | VU590 inhibits ROMK1 channels in a dose-dependent manner with an IC50 of 2… | 5 mg | V-130 | More Info |
| VU590 dihydrochloride | VU590 inhibits ROMK1 channels in a dose-dependent manner with an IC50 of 2… | 50 mg | V-130 | More Info |
| VUF 10166 | VUF 10166 is a potent and selective 5-HT3A and B receptor antagonist1. Syn… | 10 mg | V-115 | More Info |
| VUF 10166 | VUF 10166 is a potent and selective 5-HT3A and B receptor antagonist1. Syn… | 25 mg | V-115 | More Info |
| VUF 10166 | VUF 10166 is a potent and selective 5-HT3A and B receptor antagonist1. Syn… | 5 mg | V-115 | More Info |
| VUF 10166 | VUF 10166 is a potent and selective 5-HT3A and B receptor antagonist1. Syn… | 50 mg | V-115 | More Info |
| VU591 hydrochloride | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥98.5%. MW: 404.8 | 10 mg | V-126 | More Info |
| VU591 hydrochloride | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥98.5%. MW: 404.8 | 25 mg | V-126 | More Info |
| VU591 hydrochloride | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥98.5%. MW: 404.8 | 5 mg | V-126 | More Info |
| VU591 hydrochloride | VU591 is a Kir1.1 channel blocker1. Synthetic. Purity ≥98.5%. MW: 404.8 | 50 mg | V-126 | More Info |
| Waglerin-1 | Waglerin-1 blocks ε subunit of muscle adult nAChR and modulates ro… | 1 mg | STW-001 | More Info |
| Waglerin-1 | Waglerin-1 blocks ε subunit of muscle adult nAChR and modulates ro… | 10 mg | STW-001 | More Info |
| Waglerin-1 | Waglerin-1 blocks ε subunit of muscle adult nAChR and modulates ro… | 25 mg | STW-001 | More Info |
| Waglerin-1 | Waglerin-1 blocks ε subunit of muscle adult nAChR and modulates ro… | 5 mg | STW-001 | More Info |
| Wasabi Receptor Toxin | Wasabi Receptor Toxin is a cell penetrating peptide toxin activator of TRP… | 0.1 mg | STW-200 | More Info |
| Wasabi Receptor Toxin | Wasabi Receptor Toxin is a cell penetrating peptide toxin activator of TRP… | 0.5 mg | STW-200 | More Info |
| Wasabi Receptor Toxin | Wasabi Receptor Toxin is a cell penetrating peptide toxin activator of TRP… | 1 mg | STW-200 | More Info |
| Wasabi Receptor Toxin | Wasabi Receptor Toxin is a cell penetrating peptide toxin activator of TRP… | 10 mg | STW-200 | More Info |
| Wasabi Receptor Toxin | Wasabi Receptor Toxin is a cell penetrating peptide toxin activator of TRP… | 5 mg | STW-200 | More Info |
| WKYMVM | WKYMVM is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 1 mg | GPW-100 | More Info |
| WKYMVM | WKYMVM is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 10 mg | GPW-100 | More Info |
| WKYMVM | WKYMVM is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 25 mg | GPW-100 | More Info |
| WKYMVM | WKYMVM is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 5 mg | GPW-100 | More Info |
| WKYMVm | WKYMVm is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 0.5 mg | GPW-105 | More Info |
| WKYMVm | WKYMVm is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 1 mg | GPW-105 | More Info |
| WKYMVm | WKYMVm is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 10 mg | GPW-105 | More Info |
| WKYMVm | WKYMVm is a selective agonist of the formyl peptide receptors (FPR2 and FP… | 5 mg | GPW-105 | More Info |
| Wortmannin | Wortmannin is a potent and specific inhibitor of PI3-kinase1. In PC12 cell… | 1 mg | W-400 | More Info |
| Wortmannin | Wortmannin is a potent and specific inhibitor of PI3-kinase1. In PC12 cell… | 5 mg | W-400 | More Info |
| Wortmannin | Wortmannin is a potent and specific inhibitor of PI3-kinase1. In PC12 cell… | 5 x 5 mg | W-400 | More Info |
| WRW4 | WRW4 is a selective and potent antagonist of the formyl peptide receptor (… | 0.5 mg | GPW-110 | More Info |
| WRW4 | WRW4 is a selective and potent antagonist of the formyl peptide receptor (… | 1 mg | GPW-110 | More Info |
| WRW4 | WRW4 is a selective and potent antagonist of the formyl peptide receptor (… | 5 mg | GPW-110 | More Info |
| 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 |
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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