| DC36181 |
Antioxidant ZMB |
Antioxidant ZMB is an antioxidant. |
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| DC36182 |
Altimol |
Nitrefazole is a nitroimidazole derivative with the ability to inhibit aldehyde dehydrogenase. This enzyme crucial to the metabolism of alcohol and is suitable for aldehyde dehydrogenase (ALDH) related research. |
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| DC36183 |
Altinicline maleate |
Altinicline maleate is a potent neuronal nicotinic ACh receptor agonist that improves cognitive function in a MPTP-induced model of Parkinson's Disease in vivo. |
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| DC36184 |
all-trans-Capsanthin |
Capsanthin is a carotenoid found in red paprika that has diverse biological activities. It reduces hydrogen peroxide-induced production of reactive oxygen species (ROS) and phosphorylation of ERK and p38 and prevents inhibition of gap-junction intracellular communication in WB-F344 rat liver epithelial cells. Capsanthin reduces the number of colonic aberrant crypt foci and preneoplastic lesions in a rat model of N-methylnitrosourea-induced colon carcinogenesis. It also reduces ear edema in a mouse model of inflammation induced by phorbol 12-myristate 13-acetate. |
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| DC36185 |
allo-DL-Threonine |
allo-DL-Threonine is a racemic mixture of the D and L isomers of the polar essential amino acid threonine. |
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| DC36186 |
ALP 201 |
SUN-5555 is a penem --- a type of unsaturated β-lactam with a sulfur atom in the five-membered ring. SUN-5555 belongs to the penem group of antibiotics prescribed for oral usage. Enterobacteriaceae bacterial infections with cephalosporin resistance are susceptible to faropenem. Faropenem could be an effective antibiotic to treat urinary tract infections caused by extended-spectrum beta-lactamases (ESBL) producing bacteria. |
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| DC36187 |
Alprostadil ethyl ester |
Alprostadil ethyl ester is a biochemical used in the treatment of scleroderma. |
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| DC36188 |
5,6-trans-Dinoprostone |
5-trans-Prostaglandin E2 accelerates fibrinolysis by enhancing plasminogen activation mediated by tissue-type plasminogen activator. It also inhibits platelet aggregation in human PRP. |
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| DC36189 |
Algestone |
Algestone is a synthetic progestational dihydroxy derivative of Progesterone. The acetonide group possesses anti-inflammatory properties. |
|
| DC36190 |
AM 1042 |
Asukamycin is polyketide isolated from the S. nodosus subspecies asukaensis that demonstrates a broad range of antibiotic functions. It has been shown to inhibit growth of various tumor cell lines by activating caspases 8 and 3. |
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| DC36191 |
AM-3102 |
AM-3102 is an OEA analog that stimulates PPARα transcriptional activity and prolongs feeding latency. It is resistant to enzymatic hydrolysis and is as potent as OEA in enhancing transcriptional activity of PPARα and reducing food intake in free-feeding rats. AM3102 demonstrates weak affinity for the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. |
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| DC36192 |
(R)-AM-1241 |
(R)-AM1241 acts as an agonist at human CB2 receptors but an inverse agonist at rat and mouse CB2 receptors. Similar to the racemate AM1241, (R)-AM1241 produces antinociception to thermal pain but not mechanical pain in rats. The pain-reducing effect of (R)-AM1241 is blocked by the CB2-specific inhibitor SR 144528 but not by either the CB1-selective inhibitor rimonabant or the opioid receptor blocker naloxone. |
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| DC36193 |
(S)-AM-1241 |
(S)-AM1241 binds to cannabinoid (CB) receptors and is selective for CB2 over CB1. (S)-1241 acts as an agonist at human, rat, and mouse CB2 receptors but shows greater activity at human CB2 than at rat and mouse CB2 receptors. Similar to the racemate AM1241, (S)-AM1241 produces antinociception to thermal pain but not mechanical pain in rats. The pain-reducing effect of (S)-AM1241 is blocked by the CB2-specific inhibitor SR 144528 but not by either the CB1-selective inhibitor rimonabant or the opioid receptor blocker naloxone |
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| DC36194 |
AM-211 sodium |
AM-211 sodium is a novel and potent antagonist of the prostaglandin D2 receptor type 2. AM-211 is active in animal models of allergic inflammation. AM211 has high affinity for human, mouse, rat, and guinea pig DP2 and it shows selectivity over other prostanoid receptors and enzymes. AM211 exhibits good oral bioavailability in rats and dogs and dose-dependently inhibits 13,14-dihydro-15-keto-PGD(2)-induced leukocytosis in a guinea pig pharmacodynamic assay. |
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| DC36195 |
Ambamide |
Mafenide acetate is a sulfonamide that inhibits the enzyme carbonic anhydrase and is used as topical anti-infective, especially in burn therapy. |
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| DC36196 |
AI3-22370 |
Ambenonium chloride is a quaternary ammonium compound that inhibits cholinesterase activity with actions similar to those of Neostigmine but of longer duration. Ambenonium is used in the treatment of myasthenia gravis --- a chronic autoimmune neuromuscular disease that causes skeletal muscle weakness. |
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| DC36197 |
Amlodipine (±)-form maleate |
Amlodipine maleate is a long-acting dihydropyridine calcium channel blocker effective in the treatment of angina pectoris and hypertension. |
|
| DC36198 |
(+/-)-Phthalimidoamlodipine |
Phthalimidoamlodipine is an impurity of Amlodipine --- a medication used to lower blood pressure and prevent chest pain. |
|
| DC36199 |
(+)-Amlodipine |
(R)-Amlodipine is the R isomer of Amlodipine --- a medication used to lower blood pressure and prevent chest pain. |
|
| DC36200 |
Amoxydramine |
Amoxydramine is a metabolite of Diphenhydramine in humans. |
|
| DC36201 |
S-(3-Carboxypropyl)-L-cysteine |
S-(3-Carboxypropyl)-L-cysteine is a thioether derivative of L-cysteine. |
|
| DC36202 |
Amoxicillin dimer |
Amoxicillin open ring dimer is an impurity of Amoxicillin --- a β-lactam family antibiotic that is commonly used in conjunction with clavulanic acid to the treat bacterial infections. |
|
| DC36203 |
Amoxicillin clavulanate potassium |
Augmentin is a 4:1 mixture of Amoxicillin to Clavulanate which serves as a broad-spectrum antibiotic that is effective against resistant pathogens. It maintains therapeutically useful concentrations of plasma Amoxicillin for longer periods after dosing. |
|
| DC36204 |
(R,S)-AMPA |
(R,S)-AMPA is a glutamate agonist and an Ibotenic Acid homolog . The compound is the defining agonist for the AMPA subtype of glutamate receptors. It has been used as a radionuclide imaging agent but is more commonly used as an experimental tool in cell biological studies. |
|
| DC36205 |
L-(S)-AMPA |
(S)-AMPA is an active isomer of (RS)-AMPA and selective AMPA agonist. |
|
| DC36206 |
(-)-AMPA |
(R)-AMPA is an inactive isomer of (RS)-AMPA (MedKoo Cat# 573831). |
|
| DC36207 |
alpha-Aminobenzylpenicilloic acid |
Ampicilloic acid is a metabolite and impurity of the semi-synthetic antibiotic Ampicillin. |
|
| DC36208 |
Ampicillin oligomer 1 (trimer) |
Ampicillin Trimer Trisodium Salt is an impurity of Ampicillin that can be used to detect compounds or impurities related to ampicillin in bulk drug. |
|
| DC36209 |
Ampicillin EP Impurity E |
Ampicillin EP Impurity E is an impurity of Ampicillin --- an antibiotic used to prevent and treat a number of bacterial infections such as respiratory tract infections, urinary tract infections, meningitis, salmonella infections, and endocarditis. Ampicillin EP Impurity E can be used to detect compounds or impurities related to ampicillin in bulk drug. |
|
| DC36210 |
Amigal |
Migalastat is a potent inhibitor of glycolipid biosynthesis. |
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