ALOMONE LABS Non-Antibody Products — page 20 of 71

Non-Antibody Products
Page 20 of 71
  • Records 951 - 1,000 of 3,505
Name Description Size Catalog #
Diazepam Diazepam is a positive allosteric modulator of GABAA receptors at the benz… 100 mg D-215 More Info
Diazepam Diazepam is a positive allosteric modulator of GABAA receptors at the benz… 250 mg D-215 More Info
Diazepam Diazepam is a positive allosteric modulator of GABAA receptors at the benz… 50 mg D-215 More Info
5,7-Dichlorokynurenic acid 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 10 mg D-190 More Info
5,7-Dichlorokynurenic acid 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 100 mg D-190 More Info
5,7-Dichlorokynurenic acid 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 25 mg D-190 More Info
5,7-Dichlorokynurenic acid 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 50 mg D-190 More Info
5,7-Dichlorokynurenic acid monohydrate 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 10 mg D-191 More Info
5,7-Dichlorokynurenic acid monohydrate 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 100 mg D-191 More Info
5,7-Dichlorokynurenic acid monohydrate 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 25 mg D-191 More Info
5,7-Dichlorokynurenic acid monohydrate 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 250 mg D-191 More Info
5,7-Dichlorokynurenic acid monohydrate 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… 50 mg D-191 More Info
Diclofenac Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 1 g D-180 More Info
Diclofenac Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 10 g D-180 More Info
Diclofenac Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 25 g D-180 More Info
Diclofenac Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 5 g D-180 More Info
Diclofenac sodium salt Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 25 g D-181 More Info
Diclofenac sodium salt Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 5 g D-181 More Info
Diclofenac sodium salt Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… 50 g D-181 More Info
Diltiazem hydrochloride IC50 was 33 µM on CaV1.2 channels in expression systems1. Synthetic.… 1 g D-135 More Info
Diltiazem hydrochloride IC50 was 33 µM on CaV1.2 channels in expression systems1. Synthetic.… 10 g D-135 More Info
Diltiazem hydrochloride IC50 was 33 µM on CaV1.2 channels in expression systems1. Synthetic.… 5 g D-135 More Info
2,5-dimethylcelecoxib 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… 10 mg D-150 More Info
2,5-dimethylcelecoxib 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… 25 mg D-150 More Info
2,5-dimethylcelecoxib 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… 5 mg D-150 More Info
2,5-dimethylcelecoxib 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… 50 mg D-150 More Info
1,1-Dimethyl-4-phenylpiperazinium iodide DMPP activates α4 nicotinic channels expressed in Xenopus oocytes wi… 1 g D-125 More Info
1,1-Dimethyl-4-phenylpiperazinium iodide DMPP activates α4 nicotinic channels expressed in Xenopus oocytes wi… 10 g D-125 More Info
1,1-Dimethyl-4-phenylpiperazinium iodide DMPP activates α4 nicotinic channels expressed in Xenopus oocytes wi… 5 g D-125 More Info
D-IP3 IP3 Receptor agonist (active analogue). Purity ≥99%. MW: 420.09 0.1 mg D-220 More Info
DL-AP3 DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… 100 mg D-275 More Info
DL-AP3 DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… 250 mg D-275 More Info
DL-AP3 DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… 50 mg D-275 More Info
DL-AP3 DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… 500 mg D-275 More Info
DL-AP5 DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… 10 mg D-140 More Info
DL-AP5 DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… 100 mg D-140 More Info
DL-AP5 DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… 25 mg D-140 More Info
DL-AP5 DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… 5 mg D-140 More Info
DL-AP5 DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… 50 mg D-140 More Info
DL-AP7 DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 10 mg D-200 More Info
DL-AP7 DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 25 mg D-200 More Info
DL-AP7 DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 5 mg D-200 More Info
DL-AP7 DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 50 mg D-200 More Info
DMAB-anabaseine dihydrochloride DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… 1 g D-110 More Info
DMAB-anabaseine dihydrochloride DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… 10 g D-110 More Info
DMAB-anabaseine dihydrochloride DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… 10 mg D-110 More Info
DMAB-anabaseine dihydrochloride DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… 5 g D-110 More Info
DMAB-anabaseine dihydrochloride DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… 5 mg D-110 More Info
DMAB-anabaseine dihydrochloride DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… 50 mg D-110 More Info
DM-PPP DM-PPP is a selective and non-competitive antagonist of mGluR1 receptors.… 10 mg D-255 More Info
ALOMONE LABS
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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