ALOMONE LABS Non-Antibody Products — page 16 of 71
Non-Antibody Products
Page 16 of 71
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Chlormethiazole hydrochloride | Chlormethiazole both directly activates GABAA receptors (at 0.3 - 1 mM), a… | 50 mg | C-360 | More Info |
| Chlormethiazole hydrochloride | Chlormethiazole both directly activates GABAA receptors (at 0.3 - 1 mM), a… | 500 mg | C-360 | More Info |
| 5-Chloroindole | 5-Chloroindole is a potent and selective allosteric modulator of the 5-HT3… | 1 g | C-260 | More Info |
| 5-Chloroindole | 5-Chloroindole is a potent and selective allosteric modulator of the 5-HT3… | 5 g | C-260 | More Info |
| 7-Chlorokynurenic acid | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 10 mg | C-285 | More Info |
| 7-Chlorokynurenic acid | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 100 mg | C-285 | More Info |
| 7-Chlorokynurenic acid | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 25 mg | C-285 | More Info |
| 7-Chlorokynurenic acid | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 50 mg | C-285 | More Info |
| 7-Chlorokynurenic acid sodium salt | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 10 mg | C-286 | More Info |
| 7-Chlorokynurenic acid sodium salt | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 25 mg | C-286 | More Info |
| 7-Chlorokynurenic acid sodium salt | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 5 mg | C-286 | More Info |
| 7-Chlorokynurenic acid sodium salt | 7-Chlorokynurenic acid is an NMDA receptor antagonist that acts at the gly… | 50 mg | C-286 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 0.1 mg | RTC-450 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 0.5 mg | RTC-450 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 1 mg | RTC-450 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 5 mg | RTC-450 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 0.1 mg | STC-460 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 0.25 mg | STC-460 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 0.5 mg | STC-460 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 1 mg | STC-460 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 10 mg | STC-460 | More Info |
| Chlorotoxin | Chlorotoxin blocks small conductance Cl- channels of epithelial cells and… | 5 mg | STC-460 | More Info |
| Chlorpromazine hydrochloride | Chlorpromazine blocks nAChRs with IC50 ~10µM for α7 nicotinic… | 10 g | C-165 | More Info |
| Chlorpromazine hydrochloride | Chlorpromazine blocks nAChRs with IC50 ~10µM for α7 nicotinic… | 100 g | C-165 | More Info |
| Chlorpromazine hydrochloride | Chlorpromazine blocks nAChRs with IC50 ~10µM for α7 nicotinic… | 25 g | C-165 | More Info |
| Chlorpromazine hydrochloride | Chlorpromazine blocks nAChRs with IC50 ~10µM for α7 nicotinic… | 5 g | C-165 | More Info |
| Chlorpromazine hydrochloride | Chlorpromazine blocks nAChRs with IC50 ~10µM for α7 nicotinic… | 50 g | C-165 | More Info |
| Cilnidipine | Cilnidipine is an L- and N-type Ca2+-channel blocker1. Synthetic. Purity >… | 10 mg | C-135 | More Info |
| Cilnidipine | Cilnidipine is an L- and N-type Ca2+-channel blocker1. Synthetic. Purity >… | 25 mg | C-135 | More Info |
| Cilnidipine | Cilnidipine is an L- and N-type Ca2+-channel blocker1. Synthetic. Purity >… | 5 mg | C-135 | More Info |
| Cilnidipine | Cilnidipine is an L- and N-type Ca2+-channel blocker1. Synthetic. Purity >… | 50 mg | C-135 | More Info |
| CIQ | CIQ is an NR2C and NR2D selective potentiator of NMDA receptors. It enhanc… | 10 mg | C-275 | More Info |
| CIQ | CIQ is an NR2C and NR2D selective potentiator of NMDA receptors. It enhanc… | 100 mg | C-275 | More Info |
| CIQ | CIQ is an NR2C and NR2D selective potentiator of NMDA receptors. It enhanc… | 25 mg | C-275 | More Info |
| CIQ | CIQ is an NR2C and NR2D selective potentiator of NMDA receptors. It enhanc… | 5 mg | C-275 | More Info |
| CIQ | CIQ is an NR2C and NR2D selective potentiator of NMDA receptors. It enhanc… | 50 mg | C-275 | More Info |
| cis-ACBD | cis-ACBD is a weak NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 1… | 10 mg | A-281 | More Info |
| cis-ACBD | cis-ACBD is a weak NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 1… | 25 mg | A-281 | More Info |
| cis-ACBD | cis-ACBD is a weak NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 1… | 5 mg | A-281 | More Info |
| cis-ACBD | cis-ACBD is a weak NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 1… | 50 mg | A-281 | More Info |
| Citalopram | Citalopram inhibits serotonin uptake1 and blocks KV2.2 and KV2.1 channels2… | 10 mg | C-195 | More Info |
| Citalopram | Citalopram inhibits serotonin uptake1 and blocks KV2.2 and KV2.1 channels2… | 100 mg | C-195 | More Info |
| Citalopram | Citalopram inhibits serotonin uptake1 and blocks KV2.2 and KV2.1 channels2… | 25 mg | C-195 | More Info |
| Citalopram | Citalopram inhibits serotonin uptake1 and blocks KV2.2 and KV2.1 channels2… | 5 mg | C-195 | More Info |
| Citalopram | Citalopram inhibits serotonin uptake1 and blocks KV2.2 and KV2.1 channels2… | 50 mg | C-195 | More Info |
| Citalopram hydrobromide | Citalopram blocks KV2.2 and KV2.1 channels1 and inhibits 5-HT uptake2. Syn… | 1 g | C-185 | More Info |
| Citalopram hydrobromide | Citalopram blocks KV2.2 and KV2.1 channels1 and inhibits 5-HT uptake2. Syn… | 100 mg | C-185 | More Info |
| Citalopram hydrobromide | Citalopram blocks KV2.2 and KV2.1 channels1 and inhibits 5-HT uptake2. Syn… | 25 mg | C-185 | More Info |
| Citalopram hydrobromide | Citalopram blocks KV2.2 and KV2.1 channels1 and inhibits 5-HT uptake2. Syn… | 50 mg | C-185 | More Info |
| Citalopram hydrobromide | Citalopram blocks KV2.2 and KV2.1 channels1 and inhibits 5-HT uptake2. Syn… | 500 mg | C-185 | 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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