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Nor reticuline. Group: Biochemicals. Alternative Names: (1S)-1,2,3,4-tetrahydro-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-7-isoquinolinol; 2-Demethylreticuline; (-)-(S)-N-Norreticuline. Grades: Highly Purified. CAS No. 4781-58-2. Pack Sizes: 25mg. Molecular Formula: C18H21NO4. US Biological Life Sciences.
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2-(1-Phenylethyl) Nor Reticuline Dibenzyl Ether
Reticuline derivative. Group: Biochemicals. Alternative Names: (1S)-1,2,3,4-Tetrahydro-1-[(3-benzyloxy-4-methoxyphenyl)methyl]-7-benzyloxy-6-methoxy-2-phenylethyl-isoquinoline. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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1,2-Dehydro Reticuline Iodide
1,2-Dehydro Reticuline Iodide is a dehydro iminium salt derivative of Reticuline and a precursor in the synthesis of Multifloramine. Group: Biochemicals. Alternative Names: 3,4-Dihydro-7-hydroxy-1-(3-hydroxy-4-methoxybenzyl)-6-methoxy-2-methylisoquinolinium Iodide; 1,2-Dehydroreticuline Iodide; 3,4-Dihydro-7-hydroxy-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methylisoquinolinium Iodide. Grades: Highly Purified. CAS No. 21411-21-2. Pack Sizes: 5mg. US Biological Life Sciences.
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1,2-dehydroreticulinium reductase (NADPH)
Reduces the 1,2-dehydroreticulinium ion to (R)-reticuline, which is a direct precursor of morphinan alkaloids in the poppy plant. The enzyme does not catalyse the reverse reaction to any significant extent under physiological conditions. Group: Enzymes. Synonyms: 1,2-dehydroreticulinium ion reductase. Enzyme Commission Number: EC 1.5.1.27. CAS No. 130590-58-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1509; 1,2-dehydroreticulinium reductase (NADPH); EC 1.5.1.27; 130590-58-8; 1,2-dehydroreticulinium ion reductase. Cat No: EXWM-1509.
Used in the preparation of (S)-Reticuline. Group: Biochemicals. Alternative Names: 2-[4-Methoxy-3-(phenylmethoxy)phenyl]-1-(1-pyrrolidinyl)ethanone. Grades: Highly Purified. CAS No. 1206614-03-0. Pack Sizes: 10mg. US Biological Life Sciences.
Used in the preparation of (S)-Reticuline. Group: Biochemicals. Alternative Names: 2-[3-Methoxy-4-(phenylmethoxy)phenyl]-1-(1-pyrrolidinyl)-ethanone. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
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3-Benzyl oxy-4-methoxyphenyl ethyl amine
3-Benzyl oxy-4-methoxyphenyl ethyl amine is an intermediate in the synthesis of Reticuline (R188505), a tetra hydrobenzyl isoquinoline alkaloid found in opium. Group: Biochemicals. Grades: Highly Purified. CAS No. 36455-21-7. Pack Sizes: 1g, 10g. Molecular Formula: C16H19NO2. US Biological Life Sciences.
Used in the preparation of (S)-Reticuline. Group: Biochemicals. Alternative Names: 4- (2, 2-dibromoethenyl) -1-methoxy-2- (phenylmethoxy) benzene. Grades: Highly Purified. CAS No. 1206614-02-9. Pack Sizes: 100mg. US Biological Life Sciences.
Intermediate in the preparation of Reticuline and its analogs. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Reticuline
Reticuline. Group: Biochemicals. Alternative Names: (1S)-1,2,3,4-Tetrahydro-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-7-isoquinolinol; (+)-Reticuline; L-(+)-Reticuline. Grades: Highly Purified. CAS No. 485-19-8. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C19H23NO4. US Biological Life Sciences.
Worldwide
Reticuline
Reticuline shows anti-inflammatory effects through JAK2/STAT3 and NF-κB signaling pathways. Reticuline inhibits mRNA expressions of TNF-α, and IL-6 and reduces the phosphorylation levels of JAK2 and STAT3 [1]. Reticuline exhibits cardiovascular effects [2]. Uses: Scientific research. Group: Natural products. CAS No. 485-19-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N1356.
Reticuline
Reticuline shows anti-inflammatory effects through JAK2/STAT3 and NF-κB signaling pathways. Reticuline inhibits mRNA expressions of TNF-α, and IL-6 and reduces the phosphorylation levels of JAK2 and STAT3. Reticuline exhibits cardiovascular effects. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Methoxy-5-[[(1S)-2-methyl-6-methoxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline]-1-ylmethyl]phenol. Product Category: Inhibitors. Appearance: Powder. CAS No. 485-19-8. Molecular formula: C19H23NO4. Mole weight: 329.39. Purity: 0.98. IUPACName: (1S)-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol. Canonical SMILES: CN1CCC2=CC(=C(C=C2[C@@H]1CC3=CC(=C(C=C3)OC)O)O)OC. Density: 1.44 g/ml. Product ID: ACM485198. Alfa Chemistry ISO 9001:2015 Certified.
(±)-Reticuline
(±)-Reticuline (compound 3f) is a natural product obtained from Peumus boldus Molina. (±)-Reticuline can be used to synthesize S-Reticuline [1]. Uses: Scientific research. Group: Natural products. CAS No. 1699-46-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-135489.
Reticuline Hydrochloride Salt
Precursor of many aporphine and morphine-type alkaloids. Group: Biochemicals. Alternative Names: (1S)-1,2,3,4-Tetrahydro-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-7-isoquinolinol Hydrochloride; (+)-Reticuline Hydrochloride; L-(+)-Reticuline Hydrochloride; Reticulin Hydrochloride; S-(+)-Reticuline Hydrochloride; d-Reticuline Hydrochloride. Grades: Highly Purified. CAS No. 903-91-3. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
reticuline oxidase
Contains FAD. The enzyme from the plant Eschscholtzia californica binds the cofactor covalently. Acts on (S)-reticuline and related compounds, converting the N-methyl group into the methylene bridge ('berberine bridge') of (S)-tetrahydroprotoberberines. The product of the reaction, (S)-scoulerine, is a precursor of protopine, protoberberine and benzophenanthridine alkaloid biosynthesis in plants. Group: Enzymes. Synonyms: BBE; berberine bridge enzyme; berberine-bridge-forming enzyme; tetrahydroprotoberberine synthase. Enzyme Commission Number: EC 1.21.3.3. CAS No. 152232-28-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1250; reticuline oxidase; EC 1.21.3.3; 152232-28-5; BBE; berberine bridge enzyme; berberine-bridge-forming enzyme; tetrahydroprotoberberine synthase. Cat No: EXWM-1250.
(R,S)-reticuline 7-O-methyltransferase
The enzyme from the plant Papaver somniferum (opium poppy) methylates (S)- and (R)-reticuline with equal efficiency and is involved in the biosynthesis of tetrahydrobenzylisoquinoline alkaloids. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.291. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1898; (R,S)-reticuline 7-O-methyltransferase; EC 2.1.1.291. Cat No: EXWM-1898.
salutaridine synthase
A heme-thiolate enzyme (P-450). Forms the morphinan alkaloid salutaridine by intramolecular phenol oxidation of reticuline without the incorporation of oxygen into the product. Group: Enzymes. Synonyms: (R)-reticuline oxidase (C-C phenol-coupling). Enzyme Commission Number: EC 1.14.21.4. CAS No. 149433-84-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1026; salutaridine synthase; EC 1.14.21.4; 149433-84-1; (R)-reticuline oxidase (C-C phenol-coupling). Cat No: EXWM-1026.
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