522-87-2
Chemical Structure
Yohimbic acid
- CAS No.: 522-87-2
- Formula:C20H24N2O3
- Molecular Weight:340.42
IUPAC Name: (1R,2S,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-carboxylic acid
InChIKey: AADVZSXPNRLYLV-GKMXPDSGSA-N
SMILES: OC([C@@H]1[C@@]2([H])C[C@@]3([H])C4=C(CCN3C[C@]2([H])CC[C@@H]1O)C5=CC=CC=C5N4)=O
Biological Activity: Yohimbic acid is a derivative of Yohimbine Hydrochloride (HY-N0127). Yohimbic acid exhibits vasodilatory and anticancer activities. Yohimbic acid can be used for the research of cancer, inflammation and cardiovascular disease[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Yohimbic acid | 99.86% | Yohimbic acid is a derivative of Yohimbine Hydrochloride (HY-N0127). Yohimbic acid exhibits vasodilatory and anticancer activities. Yohimbic acid can be used for the research of cancer, inflammation and cardiovascular disease. | ||||||||||||||||||||
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Yohimbic acid (Standard) | ≥98% | Yohimbic acid (Standard) is the analytical standard of Yohimbic acid (HY-121936). This product is intended for research and analytical applications. Yohimbic acid is a derivative of Yohimbine Hydrochloride (HY-N0127). Yohimbic acid exhibits vasodilatory and anticancer activities. Yohimbic acid can be used for the research of cancer, inflammation and cardiovascular disease. | ||||||||||||||||||||
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- [1]. Wang S, et al. Significantly dysregulated genes in osteoarthritic labrum cells identified through gene expression profiling. Mol Med Rep. 2019;20(2):1716-1724. [Content Brief]
- [2]. Dai H, et al. Integrating single-cell multi-omics and machine learning to reveal triaptosis heterogeneity in clear cell renal cell carcinoma. Hum Genomics. Published online May 7, 2026. [Content Brief]
- [3]. RAYMOND HAMET. [Demonstration of the direct vasodilatory action of yohimbic acid and Py-tetrahydroquinoline]. C R Hebd Seances Acad Sci. 1960 Jun 27;250:4473-5. [Content Brief]