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procyanidin B1
(Q7247551)
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From Wikidata
chemical compound
Proanthocyanidin B1
EC-(4b,8)-C
Endotelon
Epicatechin(4beta->8)catechin
Procyanidin dimer B1
Epicatechin-(4beta->8)-ent-epicatechin
edit
Language
Label
Description
Also known as
default for all languages
No label defined
–
English
procyanidin B1
chemical compound
Proanthocyanidin B1
EC-(4b,8)-C
Endotelon
Epicatechin(4beta->8)catechin
Procyanidin dimer B1
Epicatechin-(4beta->8)-ent-epicatechin
Statements
instance of
type of chemical entity
0 references
subclass of
proanthocyanidins
0 references
procyanidin
0 references
2-(3,4-dihydroxyphenyl)-8-[(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
1 reference
based on heuristic
inferred from SMILES
mass
578.142
dalton
1 reference
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
8 October 2016
stereoisomer of
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,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
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2S,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
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chroman-4-yl]chromane-3,5,7-triol
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
(2S,2'S,3S,3'S,4S)-3,3',4,4'-Tetrahydro-2beta,2'beta-bis(3,4-dihydroxyphenyl)-4alpha,8'-bi[2H-1-benzopyran]-3beta,3'beta,5,5',7,7'-hexol
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
procyanidin B3
1 reference
based on heuristic
inferred from InChI
(-)-epicatechin-(4alpha->8)-(-)-epicatechin
1 reference
based on heuristic
inferred from InChI
(2S,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
1 reference
based on heuristic
inferred from InChI
(-)-procyanidin B4
1 reference
based on heuristic
inferred from InChI
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,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
1 reference
based on heuristic
inferred from InChI
Catechin-(4alpha-8)-ent-epicatechin
1 reference
based on heuristic
inferred from InChI
(2S,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol
1 reference
based on heuristic
inferred from InChI
(+)-procyanidin B2
1 reference
based on heuristic
inferred from InChI
chemical formula
C₃₀H₂₆O₁₂
1 reference
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
canonical SMILES
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
1 reference
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
isomeric 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
1 reference
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
found in taxon
Saraca asoca
1 reference
stated in
The action of Saraca asoca Roxb. de Wilde bark on the PGH2 synthetase enzyme complex of the sheep vesicular gland
Actinidia chinensis
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Annona reticulata
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Camellia sinensis
2 references
stated in
Characterization of the antioxidant functions of flavonoids and proanthocyanidins in Mauritian black teas
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Capsicum annuum
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Castanea
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Cicer arietinum
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Cucurbita pepo
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Cydonia
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Daucus carota
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Diospyros kaki
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Ficus carica
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Fragaria
2 references
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
stated in
Overall dietary polyphenol intake in a bowl of strawberries: The influence of Fragaria spp. in nutritional studies
lettuce
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Lens culinaris
2 references
stated in
Phenolic composition of the cotyledon and the seed coat of lentils ( Lens culinaris L.)
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Malus domestica
5 references
stated in
High-Performance Liquid Chromatography of the Neutral Phenolic Compounds of Low Molecular Weight in Apple Juice
stated in
Influence of processing and storage on the phenolic composition of apple juice
stated in
Polyphenolic profiles in eight apple cultivars using high-performance liquid chromatography (HPLC).
stated in
Polyphenol profiles of apple juices
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Mespilus germanica
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Musa
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Aguacate
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Phaseolus vulgaris
2 references
stated in
Identification and quantitation of phenolics from green beans by high-performance liquid chromatography
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Pisum sativum
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Prunus armeniaca
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Prunus avium
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Prunus domestica
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Prunus persica
2 references
stated in
HPLC-DAD-ESIMS analysis of phenolic compounds in nectarines, peaches, and plums
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
pomegranate
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Pyrus communis
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Ribes rubrum
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Rubus
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Solanum melongena
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Triticum aestivum
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
broad bean
2 references
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
stated in
Characterization and trypsin inhibitor activity of proanthocyanidins from Vicia faba
Cynomorium songaricum
1 reference
stated in
Polyphenolic Constituents of Cynomorium songaricum Rupr. and Antibacterial Effect of Polymeric Proanthocyanidin on Methicillin-Resistant Staphylococcus aureus
Alhagi sparsifolia
1 reference
stated in
Catechins and proanthocyanidins ofAlhagi sparsifolia. I
Areca catechu
1 reference
stated in
Structures of dimeric, trimeric, and tetrameric procyanidins from Areca catechu L.
Bischofia javanica
1 reference
stated in
Bischofianin, a dimeric dehydroellagitannin from Bischofia javanica
Cinnamomum aromaticum
1 reference
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Cinnamomum cassia
1 reference
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Cinnamomum bejolghota
1 reference
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Cinnamomum burmanni
2 references
stated in
Tannins and related compounds. XXXV. Proanthocyanidins with a doubly linked unit from the root bark of Cinnamomum sieboldii Meisner.
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Cinnamomum sieboldii
1 reference
stated in
Tannins and related compounds. XXXV. Proanthocyanidins with a doubly linked unit from the root bark of Cinnamomum sieboldii Meisner.
Cola acuminata
1 reference
stated in
Content of polyphenolic compounds in the Nigerian stimulants Cola nitida ssp. alba, Cola nitida ssp. rubra A. Chev, and Cola acuminata Schott & Endl and their antioxidant capacity
Cola nitida
1 reference
stated in
Content of polyphenolic compounds in the Nigerian stimulants Cola nitida ssp. alba, Cola nitida ssp. rubra A. Chev, and Cola acuminata Schott & Endl and their antioxidant capacity
Coleogyne ramosissima
1 reference
stated in
Flavonoid and benzophenone glycosides from Coleogyne ramosissima
Croton lechleri
1 reference
stated in
Polyphenolic compounds from Croton lechleri
Dioscorea bulbifera
1 reference
stated in
Phenolics of five yam (dioscorea) species
Dioscorea cirrhosa
2 references
stated in
Tannins and related compounds. XXXIII. Isolation and characterization of procyanidins in Dioscorea cirrhosa Lour.
stated in
Phenolics of five yam (dioscorea) species
Erythroxylum novogranatense
1 reference
stated in
(+)-catechin 3-rhamnoside from Erythroxylum novogranatense
Eucalyptus ovata
1 reference
stated in
Polyphenols from Eucalyptus ovata.
Illicium anisatum
1 reference
stated in
Prenylated flavan-3-ols and procyanidins from Illicium anisatum
Kandelia candel
1 reference
stated in
Tannins and related compounds. XXXI. Isolation and characterization of proanthocyanidins in Kandelia candel (L.) Druce.
guarana
1 reference
stated in
Antioxidant capacity and in vitro prevention of dental plaque formation by extracts and condensed tannins of Paullinia cupana.
Pinus sylvestris
2 references
stated in
Plant proanthocyanidins. Part 7. Prodelphinidins from Pinus sylvestris
stated in
Phenolics from inner bark of Pinus sylvestris
Pseudotsuga menziesii
1 reference
stated in
[5′,5′]-bisdihydroquercetin: A B-ring linked biflavonoid from Pseudotsuga menziesii
Psidium guajava
1 reference
stated in
Polymeric Proanthocyanidins from Psidium guajava
Pyrola asarifolia
1 reference
stated in
Galloylhomoarbutin and related polyphenols from Pyrola incarnata
Pyrola incarnata
1 reference
stated in
Galloylhomoarbutin and related polyphenols from Pyrola incarnata
Quercus miyagii
1 reference
stated in
Flavan-3-ol and procyanidin glycosides from quercus miyagii
Quercus phillyraeoides
1 reference
stated in
Tannins and related compounds. LXXXIII. Isolation and structures of hydrolyzable tannins, phillyraeoidins A-E from Quercus phillyraeoides.
Rhododendron dauricum
1 reference
stated in
Phenolic compounds from Rhododendron dauricum from the Baikal region
Rumex acetosa
1 reference
stated in
Proanthocyanidins and a phloroglucinol derivative from Rumex acetosa L.
Salix sieboldiana
1 reference
stated in
Acylated flavanols and procyanidins from Salix sieboldiana
Terminalia catappa
1 reference
stated in
Tannin and Related Compounds fromTerminalia catappaandTerminalia parviflora
Vaccinium vitis-idaea
1 reference
stated in
Antimicrobial activity of tannin components from Vaccinium vitis-idaea L
Zanthoxylum piperitum
1 reference
stated in
Polyphenolic constituent structures of Zanthoxylum piperitum fruit and the antibacterial effects of its polymeric procyanidin on methicillin-resistant Staphylococcus aureus
Fallopia multiflora
1 reference
stated in
Quality evaluation of Polygonum multiflorum in China based on HPLC analysis of hydrophilic bioactive compounds and chemometrics.
tomato
1 reference
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
Cinnamomum pachyphyllum
1 reference
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Cinnamomum iners
1 reference
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Cinnamon
1 reference
stated in
Tannins and related compounds. XXXIX. Procyanidin C-glucosides and an acylated flavan-3-ol glucoside from the barks of Cinnamomum cassia Blume and C. obtusifolium Nees.
Sideroxylon inerme
1 reference
stated in
Tyrosinase inhibition by extracts and constituents of Sideroxylon inerme L. stem bark, used in South Africa for skin lightening.
Paeonia rockii
1 reference
stated in
Bioactive components, antioxidant and antimicrobial activities of Paeonia rockii fruit during development
Malus pumila
5 references
stated in
Polyphenolic profiles in eight apple cultivars using high-performance liquid chromatography (HPLC).
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
stated in
Influence of processing and storage on the phenolic composition of apple juice
stated in
High-Performance Liquid Chromatography of the Neutral Phenolic Compounds of Low Molecular Weight in Apple Juice
stated in
Polyphenol profiles of apple juices
Vitis labrusca
1 reference
stated in
Phenolic Compounds in White Grapes Grown in New York
Vitis vinifera
7 references
stated in
Proanthocyanidin Dimers and Trimers from Vitis vinifera Provide Diverse Structural Motifs for the Evaluation of Dentin Biomodification
stated in
Leaf removal and wine composition of Vitis vinifera L. cv. Nero d'Avola: the volatile aroma constituents
stated in
Wine phenolics: contribution to dietary intake and bioavailability
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
stated in
The Phenolic Composition of South African Pinotage, Shiraz and Cabernet Sauvignon Wines
stated in
Direct determination of phenolic compounds in Sicilian wines by liquid chromatography with PDA and MS detection
stated in
Phenolic Compounds in White Grapes Grown in New York
physically interacts with
taste receptor type 2
subject has role
agonist
1 reference
stated in
Human Bitter Taste Receptors Are Activated by Different Classes of Polyphenols
Identifiers
InChI
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+/m0/s1
1 reference
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
InChIKey
XFZJEEAOWLFHDH-UKWJTHFESA-N
2 references
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
stated in
ChEBI release 2020-09-01
CAS Registry Number
20315-25-7
2 references
stated in
Global Substance Registration System
UNII
0566J48E7X
language of work or name
English
title
procyanidin b1
(English)
retrieved
18 November 2016
InChIKey
XFZJEEAOWLFHDH-UKWJTHFESA-N
stated in
CAS Common Chemistry
retrieved
8 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=20315-25-7
ChemSpider ID
9425166
1 reference
stated in
ChemSpider
ChemSpider ID
9425166
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
PubChem CID
11250133
2 references
stated in
PubChem
PubChem CID
11250133
language of work or name
English
title
Procyanidin B1
(English)
retrieved
18 November 2016
matched by identifier from
InChIKey
InChIKey
XFZJEEAOWLFHDH-UKWJTHFESA-N
Reaxys registry number
1339969
1 reference
stated in
ChEBI
ChEBI ID
75633
language of work or name
English
title
procyanidin B1
(English)
retrieved
8 October 2016
ChEBI ID
75633
mapping relation type
exact match
2 references
stated in
ChEMBL
ChEMBL ID
CHEMBL504937
language of work or name
English
title
PROCYANIDIN B1
(English)
retrieved
18 November 2016
matched by identifier from
International Chemical Identifier
InChI
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+/m0/s1
ChEMBL ID
CHEMBL504937
1 reference
stated in
ChEMBL
ChEMBL ID
CHEMBL504937
language of work or name
English
title
PROCYANIDIN B1
(English)
retrieved
18 November 2016
SureChEMBL ID
SCHEMBL676745
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
XFZJEEAOWLFHDH-UKWJTHFESA-N
UniChem compound ID
529701
1 reference
stated in
UniChem
MassBank accession ID
BS003943
0 references
BS003944
0 references
BS003945
0 references
BS003946
0 references
BS003947
0 references
BS003948
0 references
MSBNK-RIKEN-PR100266
0 references
MSBNK-RIKEN-PR100691
0 references
SPLASH
splash10-004r-0960640000-4a8afc17f0a82219e1c6
0 references
splash10-004i-0000090000-2d5eee8bf6041be464a5
0 references
splash10-004i-0030190000-33e24ebe4f76df6ef2bf
0 references
splash10-004i-0920000000-2a9638225ee86cfab97a
0 references
splash10-004i-0000090000-c71360b85f1250ed5912
0 references
splash10-004i-0000190000-c66411c6bdefe2c60820
0 references
splash10-004i-0910120000-904b693b4080a3b311f0
0 references
splash10-056r-0010900000-b86f17bc4193615d88ef
0 references
splash10-056r-0020900000-5050a44635efbbcd1e6d
0 references
splash10-004i-0030900000-17e8a4e37399ddefb593
0 references
splash10-0551-0690000000-0de917967e41c73de31b
0 references
splash10-052r-0191600000-fe7651fd7e7097baa30a
0 references
splash10-004i-0050960000-456238d05a29305098bb
0 references
splash10-004i-0000190000-136d2e8bbb6419a5dcb7
0 references
splash10-004i-0100090000-6fdf4ab81dd423c4334d
0 references
splash10-052r-0390200000-9f1e13b0bba9785308a3
0 references
Human Metabolome Database ID
HMDB0029754
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
XFZJEEAOWLFHDH-UKWJTHFESA-N
KNApSAcK ID
C00002917
1 reference
stated in
ChEBI
ChEBI ID
75633
language of work or name
English
title
procyanidin B1
(English)
retrieved
8 October 2016
UNII
0566J48E7X
2 references
stated in
Global Substance Registration System
UNII
0566J48E7X
language of work or name
English
title
procyanidin b1
(English)
retrieved
18 November 2016
matched by identifier from
InChIKey
InChIKey
XFZJEEAOWLFHDH-UKWJTHFESA-N
Probes And Drugs ID
PD057818
0 references
KEGG ID
C10221
1 reference
stated in
ChEBI
ChEBI ID
75633
language of work or name
English
title
procyanidin B1
(English)
retrieved
8 October 2016
LIPID MAPS ID
LMPK12030001
0 references
Freebase ID
/m/080jxcb
0 references
Microsoft Academic ID
2776882396
0 references
Sitelinks
Wikipedia
(7 entries)
edit
azbwiki
پروآنتوسیانیدین بی۱
enwiki
Procyanidin B1
eswiki
Procianidina B1
fawiki
پروآنتوسیانیدین بی۱
frwiki
Procyanidine B1
shwiki
Procijanidin B1
srwiki
Procijanidin B1
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
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