55750-85-1
Chemical Structure
Crocin III
- CAS No.: 55750-85-1
- Formula:C32H44O14
- Molecular Weight:652.68
IUPAC Name: (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-tetramethyl-16-oxo-16-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)hexadeca-2,4,6,8,10,12,14-heptaenoic acid
InChIKey: VULLCGFNYWDRHL-YJOFKXFJSA-N
SMILES: OC[C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@H]1OC[C@H]2O[C@H]([C@@H]([C@H]([C@@H]2O)O)O)OC(/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C(O)=O)=O
Biological Activity: Crocin III is a crocin isolated from Crocus sativus L. Crocins inhibit the growth of tumor cells and exhibit anti-inflammatory activity[1][2][3].
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Crocin III | 98.75% | Crocin III is a crocin isolated from Crocus sativus L. Crocins inhibit the growth of tumor cells and exhibit anti-inflammatory activity. | ||||||||||||||||||||
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Crocin III (Standard) | ≥98% | Crocin III (Standard) is the analytical standard of Crocin III. This product is intended for research and analytical applications. Crocin III is a crocin isolated from Crocus sativus L. Crocins inhibit the growth of tumor cells and exhibit anti-inflammatory activity. | ||||||||||||||||||||
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- [1]. Pu X, et al. In Vivo Production of Five Crocins in the Engineered Escherichia coli. ACS Synth Biol. 2020 May 15;9(5):1160-1168. [Content Brief]
- [2]. Hu Y, et al. Comparative anti-arthritic investigation of iridoid glycosides and crocetin derivatives from Gardenia jasminoides Ellis in Freund's complete adjuvant-induced arthritis in rats. Phytomedicine. 2019;53:223-233. [Content Brief]
- [3]. Özcan E, et al. Nonconjugated Substituents Modulate Excited-State Dynamics of Keto-Carotenoids. J Phys Chem B. 2026;130(1):205-214. [Content Brief]
Keywords
