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United States Biological

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Repaglinide-ethyl-d5
Repaglinide-ethyl-d5
United States Biological

Deuterated Repaglinide, a non-sulfonylurea oral hypoglycemic agent which is used as an antidiabetic. Melting Point: 81-111 degrees C Solubility:...

Repaglinide (Prandin, 2-Ethoxy-4-[2-[[(1S)-3-methyl-1-[2-(1-piperidinyl)butyl]amino]-2-oxoethyl]-benzoic Acid, AG-EE-623, Novonorm,)
Repaglinide (Prandin, 2-Ethoxy-4-[2-[[(1S)-3-methyl-1-[2-(1-piperidinyl)butyl]amino]-2-oxoethyl]-benzoic Acid, AG-EE-623, Novonorm,)
United States Biological

Non-sulfonylurea oral hypoglycemic agent. Used as an antidiabetic. Melting Point: 126-128 degrees C Solubility: Chloroform Storage and Stability: May be...

Reboxetine-d5, Mesylate
Reboxetine-d5, Mesylate
United States Biological

Labelled Reboxetine, a selective noradrenaline reuptake inhibitor. Melting Point: 138-140 degrees C Solubility: Chloroform, Dichloromethane, Water Storage...

Reboxetine, Mesylate
Reboxetine, Mesylate
United States Biological

A selective noradrenaline reuptake inhibitor. Melting Point: 170-171 degrees C Solubility: Chloroform, Dichloromethane, Water Storage and Stability: May be...

Rebeccamycin
Rebeccamycin
United States Biological

Rebeccamycin is an indolocarbazole isolated from Lechevalieria aerocolonigenes. It displays a selective antitumour activity against several cell lines....

Rebamipide-d4 (a-[(4-Chlorobenzoyl-d4)-amino]-1,2-dihydro-2-oxo-4-quinolinepropanoic Acid)
Rebamipide-d4 (a-[(4-Chlorobenzoyl-d4)-amino]-1,2-dihydro-2-oxo-4-quinolinepropanoic Acid)
United States Biological

Labeled Rebamipide, which shows antiulcer activity in rats. Storage and Stability: May be stored at RT for short-term only. Long-term storage is recommended...

Rebamipide (OPC-12759, Mucosta, a-[(4-Chlorobenzoyl)-amino]-1,2-dihydro-2-oxo-4-quinolinepropanoic Acid)
Rebamipide (OPC-12759, Mucosta, a-[(4-Chlorobenzoyl)-amino]-1,2-dihydro-2-oxo-4-quinolinepropanoic Acid)
United States Biological

Description: Shows antiulcer activity in rats. Source: Synthetic Purity: (same/more than)98% Appearance: White solid Solubility: DMF, DMSO Melting Point:...

Rapamycin, seco, Sodium Salt (FRAP, mTOR Inhibitor, Sirolimus)
Rapamycin, seco, Sodium Salt (FRAP, mTOR Inhibitor, Sirolimus)
United States Biological

A metabolite of Sirolimus. Solubility: Methanol, Water, Atmosphere: Argon Melting point:120-122C Method for Determining Identity: Proton NMR Spectroscopic...

Rapamycin d3, contains d0 (FRAP, mTOR Inhibitor, Sirolimus-d3 , RAPA-d3, RPM-d3)
Rapamycin d3, contains d0 (FRAP, mTOR Inhibitor, Sirolimus-d3 , RAPA-d3, RPM-d3)
United States Biological

Used as an immunosuppressant. Solubility: Methanol, Chloroform Atmosphere: Inert gas Melting Point: 103-107C Method for Determining Identity: Proton NMR...

Rapamycin (23,27-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclohentriacontine, AY 22989, Sirolimus)
Rapamycin (23,27-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclohentriacontine, AY 22989, Sirolimus)
United States Biological

Immunosuppressant, related to FK-506, but without calcineurin inhibitory activity even when complexed to FK-506 binding protein. Selectively blocks signaling...

Rapamycin (FRAP, mTOR Inhibitor, Sirolimus)
Rapamycin (FRAP, mTOR Inhibitor, Sirolimus)
United States Biological

Immunosuppressant, related to FK-506, but without calcineurin inhibitory activity even when complexed to FK-506 binding protein. Selectively blocks signaling...

Ranitidine Hydrochloride (Zantac)
Ranitidine Hydrochloride (Zantac)
United States Biological

H2 histamine receptor agonist. Assay (Dried basis C13H22N4O3S.HCl): 97.5%-102.0% Form: White to pale yellow, crystalline practically odorless power...

(1R) Ramiprilat-d5 (2-[N-(R-1-Carboxy-3-phenyl-d5-propyl)-L-alanyl]-(1R,3S,5S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid)
(1R) Ramiprilat-d5 (2-[N-(R-1-Carboxy-3-phenyl-d5-propyl)-L-alanyl]-(1R,3S,5S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid)
United States Biological

An epimer of (S)-Ramiprilat-d5. Solubility: Dimethyl Sulfoxide, Methanol Storage and Stability: May be stored at RT for short-term only. Long-term storage is...

Ramiprilat
Ramiprilat
United States Biological

A metabolite of Ramipril. Solubility: As reported Melting Point: As reported Method for Determining Identity: Proton NMR (CD3OD) Spectroscopic Analysis and...

Ramipril Acyl-b-D-glucuronide
Ramipril Acyl-b-D-glucuronide
United States Biological

An antihypertensive. An angiotensin converting enzyme (ACE) inhibitor, converted to active, diacid metabolite. This compound is not stable in an aqueous...

Ramipril (HOE-498, Altace, Cardace, Delix, Pramace, Ramace, Unipril)
Ramipril (HOE-498, Altace, Cardace, Delix, Pramace, Ramace, Unipril)
United States Biological

An antihypertensive. An angiotensin converting enzyme (ACE) inhibitor, converted to active, diacid metabolite. Melting Point: 109 degrees C Solubility:...

Ramelteon Metabolite M-II (2-Hydroxy-N-[2-[(8S)-1,6,7,8-tetrahydro-2H-cyclopenta[e]benzofuran-8-yl]ethyl]-)
Ramelteon Metabolite M-II (2-Hydroxy-N-[2-[(8S)-1,6,7,8-tetrahydro-2H-cyclopenta[e]benzofuran-8-yl]ethyl]-)
United States Biological

Melatonin MT1/MT2 receptor agonist. Sedative, hypnotic. Melting Point: 113-115 degrees C Solubility: Dimethyl Sulfoxide, Ethanol, Methanol, Storage and...

rac Ramelteon-d3 (rac N-[-[(8S)-1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-yl]ethyl]propanamide-d3, rac TAK-375-d3, rac Rozerem-d3)
rac Ramelteon-d3 (rac N-[-[(8S)-1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-yl]ethyl]propanamide-d3, rac TAK-375-d3, rac Rozerem-d3)
United States Biological

Melatonin MT1/MT2 receptor agonist. Sedative, hypnotic. Melting Point: 113-115 degrees C Solubility: Dimethyl Sulfoxide, Ethanol, Methanol, Storage and...

Raltitrexed (N-[[5-[[(1,4-Dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl]methylamino]-2-thienyl]carbonyl]-L-glutamic Acid, Tomudex, ICI-D-1694, ZD-1694)
Raltitrexed (N-[[5-[[(1,4-Dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl]methylamino]-2-thienyl]carbonyl]-L-glutamic Acid, Tomudex, ICI-D-1694, ZD-1694)
United States Biological

Folate-based inhibitor of thymidylate synthase; rapidly and extensively metabolized to its more potent polyglutamate derivatives. Antineoplastic. Melting...

Raloxifene-d4 Bismethyl Ether
Raloxifene-d4 Bismethyl Ether
United States Biological

An intermediate in the synthesis of deuterated Raloxifene, a nonsteroidal estrogen receptor mixed agonist/antagonist. Solubility: DMF, DMSO, Methanol Storage...

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