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 |
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