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| Product | Description | |
|---|---|---|
| Coclaurine | Coclaurine Inhibitor. Uses: Scientific use. Product Category: T5766. CAS No. 2196-60-3. |  |
| Coclaurine Related Compound 1 | (S)-3'-Hydroxy-N-methylcoclaurine is an structure analog of Coclaurine, a benzyltetrahydroisoquinoline alkaloid extracted from Magnolia salicifolia. Synonyms: (S)-3'-Hydroxy-N-methylcoclaurine Hydrochloride; (S)-4-[(1,2,3,4-Tetrahydro-7-hydroxy-6-methoxy-2-methyl-1-isoquinolinyl)methyl]-1,2-benzenediol Hydrochloride. Grades: > 95%. CAS No. 138644-99-2. Molecular formula: C18H22ClNO4. Mole weight: 351.8. |  |
| 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase | Involved in isoquinoline alkaloid metabolism in plants. The enzyme has also been shown to catalyse the methylation of (RS)-laudanosoline, (S)-3'-hydroxycoclaurine and (RS)-7-O-methylnorlaudanosoline. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.116. CAS No. 132084-81-2. 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-1715; 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase; EC 2.1.1.116; 132084-81-2. Cat No: EXWM-1715. |  |
| (+)-Coclaurine hydrochloride | (+)-Coclaurine ((+)-(R)-Coclaurine) hydrochloride, benzyltetrahydroisoquinoline alkaloid isolated from a variety of plant sources. (+)-Coclaurine hydrochloride has anti-aging activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (+)-(R)-Coclaurine hydrochloride; (R)-Coclaurine hydrochloride; d-Coclaurine hydrochloride. CAS No. 19894-19-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N2550A. |  |
| (-)-Coclaurine Hydrochloride | (-)-Coclaurine Hydrochloride is a benzyltetra hydroisoquinoline alkaloid extracted from Magnolia salicifolia. (-)-Coclaurine hydrochloride was shown to block postsynaptic but not presynaptic dopamine receptors in the mouse striatum. Group: Biochemicals. Alternative Names: 1,2,3,4-Tetrahydro-1-[(4-hydroxyphenyl)methyl]-6-methoxy-7-isoquinolinol. Grades: Highly Purified. CAS No. 3422-42-2. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Demethyl-Coclaurine | Demethyl-Coclaurine. CAS No. 5843-65-2. Categories: higenamine; 5843-65-2. |  CA, FL & NJ |
| (+/-)-N-methylcoclaurine | (+/-)-N-methylcoclaurine is a natural alkaloid compound found in several plants. Synonyms: (+/-)-N-methyl coclaurine; N-Methylcoclaurine; DL-N-methylcoclaurine. CAS No. 1472-62-4. Molecular formula: C18H21NO3. Mole weight: 299.36. | |
| (R)-Coclaurine | (R)-Coclaurine is a nicotinic acetylcholine receptor antagonist isolated from a variety of plant sources. Synonyms: 7-Isoquinolinol, 1,2,3,4-tetrahydro-1-[(4-hydroxyphenyl)methyl]-6-methoxy-, (1R)-. CAS No. 2196-60-3. Molecular formula: C17H19NO3. Mole weight: 285.34. | |
| (S)-coclaurine-N-methyltransferase | The enzyme is specific for the (S)-isomer of coclaurine. Norcoclaurine can also act as an acceptor. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.140. CAS No. 167398-06-3. 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-1736; (S)-coclaurine-N-methyltransferase; EC 2.1.1.140; 167398-06-3. Cat No: EXWM-1736. | |
| 3, 4-Dihydro-6-methoxy-7- (phenylmethoxy) -1-[[4- (phenylmethoxy) phenyl]methyl]-isoquinoline | 3, 4-Dihydro-6-methoxy-7- (phenylmethoxy) -1-[[4- (phenylmethoxy) phenyl]methyl]-isoquinoline is an intermediate in the synthesis of Coclaurine (C633550), a benzyltetra hydroisoquinoline alkaloid extracted from Magnolia salicifolia. Group: Biochemicals. Grades: Highly Purified. CAS No. 500577-65-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Higenamine | Higenamine. Group: Biochemicals. Alternative Names: 1,2,3,4-Tetrahydro-1-[(4-hydroxyphenyl)methyl]-6,7-Isoquinolinediol;(+/-)-1,2,3,4-Tetrahydro-1-[(4-hydroxyphenyl)methyl]-6,7-Isoquinolinediol; (+/-)-O-demethyl-Coclaurine; (RS)-Norcoclaurine; (+/-)-Demethylcoclaurine; (+/-)-Norcoclaurine; (+/-)-O-Demethylcoclaurine; dl-Demethylcoclaurine. Grades: Highly Purified. CAS No. 5843-65-2. Pack Sizes: 25mg. Molecular Formula: C16H17NO3, Molecular Weight: 271.31. US Biological Life Sciences. | Worldwide |
| Higenamine | Higenamine (Norcoclaurine), a β2-AR agonist with antioxidant capability, is a key component of the Chinese herb aconite root that prescribes for treating symptoms of heart failure in the oriental Asian countries. Higenamine is also a α1-adrenergic receptor antagonist with hypotensive effect. is a selective LSD1 inhibitor ( IC 50 =1.47 μM) that can be isolated from aconite. Higenamine hydrochloride has anti-inflammatory and antibacterial activity. Higenamine protects myocyte Apoptosis and ischemia/reperfusion (I/R) injury through selective activation of beta2-adrenergic receptor ( β2-AR ). Higenamine also reduces I/R-induced myocardial infarction in mice. Higenamine can attenuate IL-1β-induced Apoptosis through ROS-mediated PI3K/Akt signaling pathway. Higenamine protects brain cells from oxygen deprivation. Higenamine can promote bone formation in osteoporosis through the SMAD2/3 pathway. Higenamine can be used to study cancer, inflammation, cardiorenal syndrome and other diseases [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11]. Uses: Scientific research. Group: Natural products. Alternative Names: Norcoclaurine; Demethyl-Coclaurine. CAS No. 5843-65-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N2037. | |
| N-[2-[3-Methoxy-4- (phenylmethoxy) phenyl]ethyl]-4- (phenylmethoxy) benzeneacetamide | N-[2-[3-Methoxy-4- (phenylmethoxy) phenyl]ethyl]-4- (phenylmethoxy) benzeneacetamide is an intermediate in the synthesis of Coclaurine (C633550), a benzyltetra hydroisoquinoline alkaloid extracted from Magnolia salicifolia. Group: Biochemicals. Alternative Names: NSC 131667. Grades: Highly Purified. CAS No. 132257-11-5. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase | Broad substrate specificity for (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinolines; including coclaurine, norcoclaurine, isococlaurine, norarmepavine, norreticuline and tetrahydropapaverine. Both R- and S-enantiomers are methylated. The enzyme participates in the pathway leading to benzylisoquinoline alkaloid synthesis in plants. The physiological substrate is likely to be coclaurine. The enzyme was earlier termed norreticuline N-methyltransferase. However, norreticuline has not been found to occur in nature and that name does not reflect the broad specificity of the enzyme for (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinolines. Group: Enzymes. Synonyms: norreticuline N-methyltransferase. Enzyme Commission Number: EC 2.1.1.115. CAS No. 132084-82-3. 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-1714; (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase; EC 2.1.1.115; 132084-82-3; norreticuline N-methyltransferase. Cat No: EXWM-1714. | |
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