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· · COA & SDS すべての製品に適用 · 在庫品は当日出荷 プロシアニジンB2 - Moligand™, ≥90% , CAS No.29106-49-8
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥90% Synonyms
BDBM50553253｜P17914｜AKOS008901339｜ プロアントシアニジンB2｜PROCYANIDIN B2, (+)-｜(2R,2'R,3R,3'R,4R)-2,2'-bis(3,4-dihydroxyphenyl)-3、3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol | (4,8'-BI-2H-1-BENZOPYRAN)-3,3',5,5',7,7'-HEXOL, 2,2'-B
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Why this grade Moligand™, ≥90% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping 2-8℃で保管、アルゴン充填 Ships 濡れた氷 Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
概要 プロシアニジンB2は、顆粒膜細胞のアポトーシスを減少させ、オートファジーのプロセスを誘導する強力で有益な役割を発揮し、糖尿病合併症に対して様々な強力な保護薬理作用を発揮する。
Specifications 同義語
BDBM50553253｜P17914｜AKOS008901339｜ プロアントシアニジンB2｜PROCYANIDIN B2, (+)-｜(2R,2'R,3R,3'R,4R)-2,2'-bis(3,4-dihydroxyphenyl)-3、3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol | (4,8'-BI-2H-1-BENZOPYRAN)-3,3',5,5',7,7'-HEXOL, 2,2'-B
生化学的・生理学的メカニズム
プロシアニジンB2は、顆粒膜細胞のアポトーシスを減少させ、オートファジーのプロセスを誘導する強力で有益な役割を発揮し、糖尿病合併症に対する様々な強力な保護薬理作用を発揮する。In vitro：プロシアニジンB2投与による
名前と識別子 パブケム・シド 504756878 パブケム・シド・ウル https://pubchem.ncbi.nlm.nih.gov/substance/504756878 カノニカル・スマイル C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O IUPAC Name (2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol InChIKey XFZJEEAOWLFHDH-NFJBMHMQSA-N INCHI 1S/C30H26O12/c31-13-7-20(37)24-23(8-13)41-29(12-2-4-16(33)19(36)6-12)27(40)26(24)25-21(38)10-17(34)14-9-22(39)28(42-30(14)25)11-1-3-15(32)18(35)5-11/h1-8,10,22,26-29,31-40H,9H2/t22-,26-,27-,28-,29-/m1/s1 異性体SMILES C1[C@H]([C@H](OC2=C1C(=CC(=C2[C@@H]3[C@H]([C@H](OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O PubChem CID 122738 分子量 578.52
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Phenylpropanoids and polyketides 分類 Flavonoids Subclass Biflavonoids and polyflavonoids Intermediate Tree Nodes Not available Direct Parent Biflavonoids and polyflavonoids Alternative Parents B-type proanthocyanidins Catechins 3'-hydroxyflavonoids 3-hydroxyflavonoids 4'-hydroxyflavonoids 5-hydroxyflavonoids 7-hydroxyflavonoids 1-benzopyrans Catechols 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Benzene and substituted derivatives Secondary alcohols Oxacyclic compounds Polyols Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents B-type proanthocyanidin - Bi- and polyflavonoid skeleton - Proanthocyanidin - Catechin - Flavan-3-ol - Hydroxyflavonoid - 3'-hydroxyflavonoid - 7-hydroxyflavonoid - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - 3-hydroxyflavonoid - Flavan - Chromane - 1-benzopyran - Benzopyran - Catechol - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Ether - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound 説明 This compound belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''. External Descriptors Proanthocyanidins Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3 D構造 関連ターゲット（人間） 関連ターゲット（非人間） 作用メカニズム 証明書（CoA、COO、BSE/TSEと分析図） 化学的性質と物理的性質 屈折率 1.8 沸点（°C） 955.32° C 融点（°C） 197-198°C 分子量 578.500 g/mol XLogP3 2.400 Hydrogen Bond Donor Count 10 Hydrogen Bond Acceptor Count 12 Rotatable Bond Count 3 Exact Mass 578.142 Da Monoisotopic Mass 578.142 Da Topological Polar Surface Area 221.000 Ų Heavy Atom Count 42 Formal Charge 0 Complexity 925.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 5 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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