ALOMONE LABS Non-Antibody Products — page 40 of 47
Non-Antibody Products
Page 40 of 47
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Retigabine dihydrochloride | Retigabine is a potent and selective KCNQ (KV7, M-) channel modulator (enh… | 100 mg | R-101 | More Info |
| Retigabine dihydrochloride | Retigabine is a potent and selective KCNQ (KV7, M-) channel modulator (enh… | 25 mg | R-101 | More Info |
| Retigabine dihydrochloride | Retigabine is a potent and selective KCNQ (KV7, M-) channel modulator (enh… | 250 mg | R-101 | More Info |
| Retigabine dihydrochloride | Retigabine is a potent and selective KCNQ (KV7, M-) channel modulator (enh… | 50 mg | R-101 | More Info |
| Ricasetron | Ricasetron is a 5-HT3 antagonist with Ki 0.32 nM1. Synthetic. Purity >99%.… | 10 mg | R-150 | More Info |
| Ricasetron | Ricasetron is a 5-HT3 antagonist with Ki 0.32 nM1. Synthetic. Purity >99%.… | 25 mg | R-150 | More Info |
| Ricasetron | Ricasetron is a 5-HT3 antagonist with Ki 0.32 nM1. Synthetic. Purity >99%.… | 5 mg | R-150 | More Info |
| Ricasetron | Ricasetron is a 5-HT3 antagonist with Ki 0.32 nM1. Synthetic. Purity >99%.… | 50 mg | R-150 | More Info |
| RJR 2403 oxalate | RJR 2403 oxalate activates α4/β2 nAChR EC50 ~ 16 µM1. Syn… | 10 mg | R-115 | More Info |
| RJR 2403 oxalate | RJR 2403 oxalate activates α4/β2 nAChR EC50 ~ 16 µM1. Syn… | 25 mg | R-115 | More Info |
| RJR 2403 oxalate | RJR 2403 oxalate activates α4/β2 nAChR EC50 ~ 16 µM1. Syn… | 5 mg | R-115 | More Info |
| RJR 2403 oxalate | RJR 2403 oxalate activates α4/β2 nAChR EC50 ~ 16 µM1. Syn… | 50 mg | R-115 | More Info |
| RO-3 | RO-3 is a potent and selective antagonist of the P2X3 and P2X2 / 3 recepto… | 10 mg | R-190 | More Info |
| RO-3 | RO-3 is a potent and selective antagonist of the P2X3 and P2X2 / 3 recepto… | 25 mg | R-190 | More Info |
| RO-3 | RO-3 is a potent and selective antagonist of the P2X3 and P2X2 / 3 recepto… | 5 mg | R-190 | More Info |
| RO-3 | RO-3 is a potent and selective antagonist of the P2X3 and P2X2 / 3 recepto… | 50 mg | R-190 | More Info |
| Ro46-8443 | Ro 46-8443 is a non-peptide, selective and competitive antagonist of ET-B… | 1 mg | R-185 | More Info |
| Ro46-8443 | Ro 46-8443 is a non-peptide, selective and competitive antagonist of ET-B… | 10 mg | R-185 | More Info |
| Ro46-8443 | Ro 46-8443 is a non-peptide, selective and competitive antagonist of ET-B… | 25 mg | R-185 | More Info |
| Ro46-8443 | Ro 46-8443 is a non-peptide, selective and competitive antagonist of ET-B… | 5 mg | R-185 | More Info |
| Ro-51 | Ro-51 is a highly potent and selective antagonist of P2X3 and P2X2 / 3 rec… | 10 mg | R-195 | More Info |
| Ro-51 | Ro-51 is a highly potent and selective antagonist of P2X3 and P2X2 / 3 rec… | 25 mg | R-195 | More Info |
| Ro-51 | Ro-51 is a highly potent and selective antagonist of P2X3 and P2X2 / 3 rec… | 5 mg | R-195 | More Info |
| Ro-51 | Ro-51 is a highly potent and selective antagonist of P2X3 and P2X2 / 3 rec… | 50 mg | R-195 | More Info |
| Ro 8-4304 hydrochloride | Ro 8-4304 is a non-competitive, state-dependent, voltage-independent NMDA… | 10 mg | R-165 | More Info |
| Ro 8-4304 hydrochloride | Ro 8-4304 is a non-competitive, state-dependent, voltage-independent NMDA… | 25 mg | R-165 | More Info |
| Ro 8-4304 hydrochloride | Ro 8-4304 is a non-competitive, state-dependent, voltage-independent NMDA… | 5 mg | R-165 | More Info |
| Ro 8-4304 hydrochloride | Ro 8-4304 is a non-competitive, state-dependent, voltage-independent NMDA… | 50 mg | R-165 | More Info |
| Ro 25-6981 maleate | Ro 25-6981 maleate is a potent, NR2B-subunit selective, activity dependent… | 10 mg | R-180 | More Info |
| Ro 25-6981 maleate | Ro 25-6981 maleate is a potent, NR2B-subunit selective, activity dependent… | 100 mg | R-180 | More Info |
| Ro 25-6981 maleate | Ro 25-6981 maleate is a potent, NR2B-subunit selective, activity dependent… | 25 mg | R-180 | More Info |
| Ro 25-6981 maleate | Ro 25-6981 maleate is a potent, NR2B-subunit selective, activity dependent… | 250 mg | R-180 | More Info |
| Ro 25-6981 maleate | Ro 25-6981 maleate is a potent, NR2B-subunit selective, activity dependent… | 5 mg | R-180 | More Info |
| Ro 25-6981 maleate | Ro 25-6981 maleate is a potent, NR2B-subunit selective, activity dependent… | 50 mg | R-180 | More Info |
| Roscovitine | Roscovitine is an olomoucine-related purine flavopiridol. In contrast to O… | 1 mg | R-300 | More Info |
| Roscovitine | Roscovitine is an olomoucine-related purine flavopiridol. In contrast to O… | 5 mg | R-300 | More Info |
| Roscovitine | Roscovitine is an olomoucine-related purine flavopiridol. In contrast to O… | 5 x 1 mg | R-300 | More Info |
| Rosiglitazone | Rosiglitazone blocks KV4.3 channels with an IC50 = 24.5 µM1, Kir6.1… | 10 mg | R-125 | More Info |
| Rosiglitazone | Rosiglitazone blocks KV4.3 channels with an IC50 = 24.5 µM1, Kir6.1… | 100 mg | R-125 | More Info |
| Rosiglitazone | Rosiglitazone blocks KV4.3 channels with an IC50 = 24.5 µM1, Kir6.1… | 25 mg | R-125 | More Info |
| Rosiglitazone | Rosiglitazone blocks KV4.3 channels with an IC50 = 24.5 µM1, Kir6.1… | 50 mg | R-125 | More Info |
| RQ 00203078 | RQ 00203078 is a potent and selective TRPM8 antagonist, shown to inhibit m… | 10 mg | R-170 | More Info |
| RQ 00203078 | RQ 00203078 is a potent and selective TRPM8 antagonist, shown to inhibit m… | 100 mg | R-170 | More Info |
| RQ 00203078 | RQ 00203078 is a potent and selective TRPM8 antagonist, shown to inhibit m… | 25 mg | R-170 | More Info |
| RQ 00203078 | RQ 00203078 is a potent and selective TRPM8 antagonist, shown to inhibit m… | 5 mg | R-170 | More Info |
| RQ 00203078 | RQ 00203078 is a potent and selective TRPM8 antagonist, shown to inhibit m… | 50 mg | R-170 | More Info |
| 3R12Rα-Pompilidotoxin | 3R12Rα-PMTX slows NaV channel inactivation without changing the peak… | 1 mg | P-176 | More Info |
| 3R12Rα-Pompilidotoxin | 3R12Rα-PMTX slows NaV channel inactivation without changing the peak… | 10 mg | P-176 | More Info |
| 3R12Rα-Pompilidotoxin | 3R12Rα-PMTX slows NaV channel inactivation without changing the peak… | 5 mg | P-176 | More Info |
| (RS)-AMPA | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >99% (H… | 10 mg | A-265 | More Info |
| (RS)-AMPA | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >99% (H… | 25 mg | A-265 | More Info |
| (RS)-AMPA | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >99% (H… | 5 mg | A-265 | More Info |
| (RS)-AMPA | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >99% (H… | 50 mg | A-265 | More Info |
| (RS)-AMPA hydrobromide | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >95%. M… | 1 mg | A-266 | More Info |
| (RS)-AMPA hydrobromide | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >95%. M… | 10 mg | A-266 | More Info |
| (RS)-AMPA hydrobromide | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >95%. M… | 25 mg | A-266 | More Info |
| (RS)-AMPA hydrobromide | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >95%. M… | 5 mg | A-266 | More Info |
| (RS)-AMPA hydrobromide | (RS)-AMPA is a selective AMPA receptor agonist1. Synthetic. Purity >95%. M… | 50 mg | A-266 | More Info |
| RS 56812 hydrochloride | RS 56812 is a highly potent and selective 5-HT3 partial agonist1. Syntheti… | 10 mg | R-130 | More Info |
| RS 56812 hydrochloride | RS 56812 is a highly potent and selective 5-HT3 partial agonist1. Syntheti… | 25 mg | R-130 | More Info |
| RS 56812 hydrochloride | RS 56812 is a highly potent and selective 5-HT3 partial agonist1. Syntheti… | 5 mg | R-130 | More Info |
| RS 56812 hydrochloride | RS 56812 is a highly potent and selective 5-HT3 partial agonist1. Syntheti… | 50 mg | R-130 | More Info |
| (RS)-(Tetrazol-5-yl)glycine | (RS)-(Tetrazol-5-yl)glycine is a highly potent and selective NMDA receptor… | 10 mg | T-205 | More Info |
| (RS)-(Tetrazol-5-yl)glycine | (RS)-(Tetrazol-5-yl)glycine is a highly potent and selective NMDA receptor… | 25 mg | T-205 | More Info |
| (RS)-(Tetrazol-5-yl)glycine | (RS)-(Tetrazol-5-yl)glycine is a highly potent and selective NMDA receptor… | 5 mg | T-205 | More Info |
| (RS)-(Tetrazol-5-yl)glycine | (RS)-(Tetrazol-5-yl)glycine is a highly potent and selective NMDA receptor… | 50 mg | T-205 | More Info |
| Ruthenium red | RYR antagonist. Purity ≥98%. MW: 786.35 | 5 mg | R-175 | More Info |
| RY796 | RY796 is a blocker of KV2.2 and KV2.1 channels, with IC50 of 0.09 and 0.25… | 10 mg | R-160 | More Info |
| RY796 | RY796 is a blocker of KV2.2 and KV2.1 channels, with IC50 of 0.09 and 0.25… | 25 mg | R-160 | More Info |
| RY796 | RY796 is a blocker of KV2.2 and KV2.1 channels, with IC50 of 0.09 and 0.25… | 5 mg | R-160 | More Info |
| RY796 | RY796 is a blocker of KV2.2 and KV2.1 channels, with IC50 of 0.09 and 0.25… | 50 mg | R-160 | More Info |
| Ryanodine | Ryanodine is a blocker of the Ryanodine receptor (RyR) Ca2+ release channe… | 1 mg | R-500 | More Info |
| Ryanodine | Ryanodine is a blocker of the Ryanodine receptor (RyR) Ca2+ release channe… | 5 mg | R-500 | More Info |
| Ryanodine | Ryanodine is a blocker of the Ryanodine receptor (RyR) Ca2+ release channe… | 5 x 1 mg | R-500 | More Info |
| Ryanodine | Ryanodine is a blocker of the Ryanodine receptor (RyR) Ca2+ release channe… | 0.5 mg | R-500 | 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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