CAS 86631-38-1
:Cinnamtannin A2
Description:
Cinnamtannin A2 is a polyphenolic compound classified as a type of tannin, specifically derived from cinnamon bark. It is known for its complex structure, which includes multiple phenolic units linked by carbon-carbon bonds. This compound exhibits a range of biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties, making it of interest in both food science and pharmacology. Cinnamtannin A2 is soluble in water and organic solvents, which enhances its potential applications in various formulations. Its ability to interact with proteins and other macromolecules contributes to its effectiveness in stabilizing emulsions and enhancing the shelf life of products. Additionally, research suggests that Cinnamtannin A2 may have potential health benefits, including the modulation of metabolic processes and the promotion of cardiovascular health. However, further studies are needed to fully understand its mechanisms of action and potential therapeutic applications. Overall, Cinnamtannin A2 represents a significant area of interest in natural product chemistry and its applications in health and nutrition.
Formula:C60H50O24
InChI:InChI=1S/C60H50O24/c61-23-13-34(71)42-41(14-23)81-55(20-2-6-26(63)31(68)10-20)51(78)48(42)44-36(73)17-38(75)46-50(53(80)57(83-59(44)46)22-4-8-28(65)33(70)12-22)47-39(76)18-37(74)45-49(52(79)56(84-60(45)47)21-3-7-27(64)32(69)11-21)43-35(72)16-29(66)24-15-40(77)54(82-58(24)43)19-1-5-25(62)30(67)9-19/h1-14,16-18,40,48-57,61-80H,15H2/t40-,48-,49+,50-,51-,52-,53-,54-,55-,56-,57-/m1/s1
InChI key:InChIKey=QFLMUASKTWGRQE-JNIIMKSASA-N
SMILES:O[C@@H]1[C@H](C=2C(=C(C(O)=CC2O)[C@H]3C=4C(O[C@@H]([C@@H]3O)C5=CC(O)=C(O)C=C5)=CC(O)=CC4O)O[C@@H]1C6=CC(O)=C(O)C=C6)C7=C8C([C@@H]([C@@H](O)[C@H](O8)C9=CC(O)=C(O)C=C9)C%10=C%11C(C[C@@H](O)[C@H](O%11)C%12=CC(O)=C(O)C=C%12)=C(O)C=C%10O)=C(O)C=C7O
Synonyms:- (2R,2′R,2′′R,2′′′R,3R,3′R,3′′R,3′′′R,4R,4′R,4′′S)-2,2′,2′′,2′′′-Tetrakis(3,4-dihydroxyphenyl)-3,3′,3′′,3′′′,4,4′,4′′,4′′′-octahydro[4,8′:4′,8′′:4′′,8′′′-quater-2H-1-benzopyran]-3,3′,3′′,3′′′,5,5′,5′′,5′′′,7,7′,7′′,7′′′-dodecol
- Cinnamtannin A<sub>2</sub>
- Cinnamtannin I
- Epicatechin tetramer
- [4,8':4',8'':4'',8'''-quater-2H-1-benzopyran]-3,3',3'',3''',5,5',5'',5''',7,7',7'',7'''-dodecol, 2,2',2'',2'''-tetrakis(3,4-dihydroxyphenyl)-3,3',3'',3''',4,4',4'',4'''-octahydro-, (2R,2'R,2''R,2'''R,3R,3'R,3''R,3'''R,4R,4'R,4''S)-
- [4,8′:4′,8′′:4′′,8′′′-Quater-2H-1-benzopyran]-3,3′,3′′,3′′′,5,5′,5′′,5′′′,7,7′,7′′,7′′′-dodecol, 2,2′,2′′,2′′′-tetrakis(3,4-dihydroxyphenyl)-3,3′,3′′,3′′′,4,4′,4′′,4′′′-octahydro-, (2R,2′R,2′′R,2′′′R,3R,3′R,3′′R,3′′′R,4R,4′R,4′′S)-
- [4,8′:4′,8′′:4′′,8′′′-Quater-2H-1-benzopyran]-3,3′,3′′,3′′′,5,5′,5′′,5′′′,7,7′,7′′,7′′′-dodecol, 2,2′,2′′,2′′′-tetrakis(3,4-dihydroxyphenyl)-3,3′,3′′,3′′′,4,4′,4′′,4′′′-octahydro-, stereoisomer
- (2R,2'R,2''R,2'''R,3R,3'R,3''R,3'''R,4R,4'R,4''S)-2,2',2'',2'''-tetrakis(3,4-dihydroxyphenyl)-3,3',3'',3''',4,4',4'',4'''-octahydro-2H,2'H,2''H,2'''H-4,8':4',8'':4'',8'''-quaterchromene-3,3',3'',3''',5,5',5'',5''',7,7',7'',7'''-dodecol
- Cinnamtannin A2
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Found 4 products.
Cinnamtannin A2
CAS:<p>Cinnamtannin A2, a tetrameric procyanidin, boosts GLP-1, insulin, CRH expression, and has antioxidant, anti-diabetic, nephroprotective properties.</p>Formula:C60H50O24Color and Shape:SolidMolecular weight:1155.02Cinnamtannin a2
CAS:Oxygen-heterocyclic compoundFormula:C60H50O24Purity:≥ 85.0 % (HPLC)Color and Shape:PowderMolecular weight:1155.04Cinnamtannin A2
CAS:<p>Cinnamtannin A2 is a type of proanthocyanidin, which is a polyphenolic compound derived from the bark of the cinnamon tree, Cinnamomum zeylanicum. This compound belongs to the class of condensed tannins and is primarily extracted from plant sources utilizing advanced purification techniques. The mode of action of Cinnamtannin A2 is predominantly based on its ability to scavenge free radicals and inhibit oxidative stress, making it a potent antioxidant. Additionally, Cinnamtannin A2 exhibits significant anti-inflammatory properties by modulating various signaling pathways involved in the inflammatory response.</p>Formula:C60H50O24Purity:Min. 95%Molecular weight:1,155.02 g/mol



