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| Product | Description | |
|---|---|---|
| Serpentine bitartrate | Serpentine bitartrate. Group: Biochemicals. Alternative Names: Serpentine hydrogen tartrate. Grades: Highly Purified. CAS No. 58782-36-8. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C21H21N2O3·C4H5O6. US Biological Life Sciences. |  Worldwide |
| Ajmalicine | Ajmalicine (Raubasine) is a potent adrenolytic agent which preferentially blocks α 1 -adrenoceptor. Ajmalicine is an reversible but non-competitive nicotine receptor full inhibitor, with an IC 50 of 72.3 μM. Ajmalicine also can be used as anti-hypertensive, and serpentine, with sedative activity [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Raubasine. CAS No. 483-04-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N1919. |  |
| MS438 | MS438 is a potent thyrotropin receptor ( TSHR ) agonist with an EC 50 of 53 nM. MS438 binds to the serpentine portion of the TSHR. MS438 induces T4 secretion in mice [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 512840-45-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-114918. | |
| Ajmaline | Ajmaline is an alkaloid which could be extracted from Rauwolfia serpentina. It is an antiarrhythmic agent, acting through changing the shreshold and the shape of cardiac action potentials. Synonyms: Cardiorythmine; Ajmalin; Gilurytmal; Raugalline. Grades: >95%. CAS No. 4360-12-7. Molecular formula: C20H26N2O2. Mole weight: 326.43. |  |
| Ajmaline | An antiarrhythmic agent isolated from Rauwolfia serpentina. Group: Biochemicals. Alternative Names: (17R,21α-Ajmalan-17,21-diol; (+)-Ajmaline; Cardiorythmine; Gilurytmal; Ignazin; Merabitol; NSC 15627; Raugalline; Rauwolfin; Rauwolfine; Rhytmaton; Ritmos; Rytmalin; Siddiqui; Tachmalin; Takycor. Grades: Highly Purified. CAS No. 4360-12-7. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| iso-Reserpiline | Reserpine is a plant alkaloid that was first isolated from the roots of Rauwolfia serpentina. It is used in the treatment of high blood pressure and psychosis. Reserpine binds to cholinergic receptors and blocks the release of neurotransmitters, leading to the symptoms of psychosis. Reserpine also acts as an antagonist at dopamine receptors, which may be responsible for its antipsychotic effects. Reserpine has been shown to have potent antitumor activity against a variety of cancer cell lines in vitro and in vivo, including breast carcinoma cells. The mechanism of action is not yet fully understood but may involve inhibition of DNA synthesis or protein synthesis. Reserpine can be synthesized by hydrolysis of iso-reserpiline with hydrochloric acid, followed by chromatographic purification. Iso-reserpiline is a mixture of two compounds: neisosperma and apocynaceae, which are both in. Group: Other alkaloids. CAS No. 572-67-8. Molecular formula: C23H28N2O5. Mole weight: 412.48 g/mol. Canonical SMILES: C[C@H]1[C@@H]2CN3CCC4=C ([C@@H]3C[C@@H]2C (=CO1)C (=O)OC)NC5=CC (=C (C=C45)OC)OC. Catalog: ACM572678. |  |
| Reserpine | An indole alkaloid found in Rauwolfia serpentina. Inhibits vesicular uptake of catecholamines and serotonin. Reserpine is reasonably anticipated to be a human carcinogen. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 50-55-5. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Reserpine-d9 | Labeled Reserpine. An indole alkaloid found in Rauwolfia serpentina. Inhibits vesicular uptake of catecholamines and serotonin. Reserpine is reasonably anticipated to be a human carcinogen. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 84759-11-5. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
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