549-84-8
Chemical Structure
β-Yohimbine
Synonym(s): Amsonin; Amsonine; NSC 93133
- CAS No.: 549-84-8
- Formula:C21H26N2O3
- Molecular Weight:354.44
IUPAC Name: methyl (1R,2R,4aR,13bS,14aS)-2-hydroxy-1,2,3,4,4a,5,7,8,13,13b,14,14a-dodecahydroindolo[2',3':3,4]pyrido[1,2-b]isoquinoline-1-carboxylate
InChIKey: BLGXFZZNTVWLAY-MQPLHJKPSA-N
SMILES: COC([C@@H]1[C@@]2([H])C[C@@]3([H])C4=C(CCN3C[C@]2([H])CC[C@H]1O)C5=C(C=CC=C5)N4)=O
Biological Activity: β-Yohimbine (Amsonin; Amsonine; NSC 93133) is a yohimbine-type indole alkaloid derived from the bark of various plants. β-Yohimbine can serve as a substrate for microbial 10-hydroxylation by Streptomyces rimosus, and is used in alkaloid biotransformation studies[1][2][3][4].
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β-Yohimbine | β-Yohimbine (Amsonin; Amsonine; NSC 93133) is a yohimbine-type indole alkaloid derived from the bark of various plants. β-Yohimbine can serve as a substrate for microbial 10-hydroxylation by Streptomyces rimosus, and is used in alkaloid biotransformation studies. | |||||||||||||||||||||
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References
- [1]. de Almeida Carlos L, et al. Rauvolfia grandiflora (apocynaceae) extract interferes with staphylococcal density, enterotoxin production and antimicrobial activity. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]. 2010 Jul;41(3):612-20.
- [2]. PATTERSON EL, et al. THE MICROBIOLOGICAL TRANSFORMATION OF SOME YOHIMBINE-TYPE ALKALOIDS. Arch Biochem Biophys. 1963 Oct;103:117-23.
- [3]. Yamamoto K, et al. Seasonal variation affects the accumulation of alkaloids in Amsonia elliptica. J Plant Res. 2026 Jul;139(4):645-653.
- [4]. Shin D, et al. Multi-Class Determination of 64 Illicit Compounds in Dietary Supplements Using Liquid Chromatography-Tandem Mass Spectrometry. Molecules (Basel, Switzerland). 2020 Sep 24;25(19):4399.
