trans-Crocetin (β-D-gentiobiosyl) ester manufacturers
- Crocin III
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- $129.00
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2026-07-17
- CAS:55750-85-1
- Purity: 99.91%
- Supply Ability: 10g
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| | trans-Crocetin (β-D-gentiobiosyl) ester Basic information |
| Product Name: | trans-Crocetin (β-D-gentiobiosyl) ester | | Synonyms: | Crocetin-mono-(β-D-gentiobiosyl)-ester;(2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptaenedioic acid 16-(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl) ester;8,8'-Diapo-ψ,ψ-carotene-8,8'-dioic acid 8-(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl) ester;Crocetin glucosylglucoside;Crocin-3;trans-Crocetin (β-D-gentiobiosyl) ester;β-D-Glucopyranose, 6-O-β-D-glucopyranosyl-, 1-[hydrogen (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-tetramethyl-2,4,6,8,10,12,14-hexadecaheptaenedioate];inhibit,Crocin III,Inhibitor | | CAS: | 55750-85-1 | | MF: | C32H44O14 | | MW: | 652.69 | | EINECS: | | | Product Categories: | | | Mol File: | 55750-85-1.mol |  |
| | trans-Crocetin (β-D-gentiobiosyl) ester Chemical Properties |
| Boiling point | 914.6±65.0 °C(Predicted) | | density | 1.39±0.1 g/cm3(Predicted) | | pka | 4.69±0.19(Predicted) | | form | Solid | | color | Light yellow to orange | | InChIKey | VULLCGFNYWDRHL-LTUXAWLRNA-N |
| | trans-Crocetin (β-D-gentiobiosyl) ester Usage And Synthesis |
| Uses | Crocin III is a crocetin from saffron (Crocus sutivus L.). Crocetins inhibit cell growth of tumor cells and has anti-inflammatory activity. Crocins serve as spices and coloring agents[1][2][3]. | | Definition | ChEBI: Beta-D-gentiobiosyl crocetin is a dicarboxylic acid monoester resulting from the formal condensation of one of the carboxylic acid groups of crocetin with the anomeric hydroxy group of beta-D-gentiobiose. It is a dicarboxylic acid monoester, a glycoside and a disaccharide derivative. It is functionally related to a crocetin and a gentiobiose. It is a conjugate acid of a beta-D-gentiobiosyl crocetin(1-). | | References | [1] Xiangdong Pu, et al. In Vivo Production of Five Crocins in the Engineered Escherichia coli. ACS Synth Biol. 2020 May 15;9(5):1160-1168. DOI:10.1021/acssynbio.0c00039
[2] J Escribano, et al. Crocin, safranal and picrocrocin from saffron (Crocus sativus L.) inhibit the growth of human cancer cells in vitro. Cancer Lett. 1996 Feb 27;100(1-2):23-30. DOI:10.1016/0304-3835(95)04067-6
[3] Yaya Hu, 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 Feb;53:223-233. DOI:10.1016/j.phymed.2018.07.005 |
| | trans-Crocetin (β-D-gentiobiosyl) ester Preparation Products And Raw materials |
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