Procyanidin B-2

group of stereoisomers with the chemical formula C₃₀H₂₆O₁₂
ChemicalSubstance group_of_stereoisomers Q104252503
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Procyanidin B-2

Summary

Procyanidin B-2 is a group of stereoisomers[1].

Key Facts

  • Procyanidin B-2's instance of is recorded as group of stereoisomers[2].
  • Procyanidin B-2's canonical SMILES is recorded as OC=1C=C(O)C2=C(OC(C3=CC=C(O)C(O)=C3)C(O)C2C=4C(O)=CC(O)=C5C4OC(C6=CC=C(O)C(O)=C6)C(O)C5)C1[3].
  • Procyanidin B-2's InChI is recorded as 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[4].
  • Procyanidin B-2's InChIKey is recorded as XFZJEEAOWLFHDH-ATEOAPGCSA-N[5].
  • Procyanidin B-2's chemical formula is recorded as C₃₀H₂₆O₁₂[6].
  • Procyanidin B-2's subclass of is recorded as (4→8)-proanthocyanidin[7].
  • Procyanidin B-2's subclass of is recorded as 8C-substituted flavan[8].
  • Procyanidin B-2's PubChem CID is recorded as 5320711[9].
  • Procyanidin B-2's found in taxon is recorded as Saraca indica[10].
  • Procyanidin B-2's found in taxon is recorded as Cassia javanica var. javanica[11].
  • Procyanidin B-2's isomeric SMILES is recorded as Oc1cc(O)c2c(c1)OC@HC@HC2c1c(O)cc(O)c2c1OC@HC@HC2C@HC@HC2c1c(O)cc(O)c2c1OC@HC@HC2">[12].
  • Procyanidin B-2's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+578.142426272'}[13].
  • Procyanidin B-2's SureChEMBL ID is recorded as 13006354[14].
  • Procyanidin B-2's UniChem compound ID is recorded as 24740247[15].
  • Procyanidin B-2's Probes And Drugs ID is recorded as PD159969[16].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . The action of Saraca asoca Roxb. de Wilde bark on the PGH2 synthetase enzyme complex of the sheep vesicular gland. wikidata.org.
  10. [11] . Tannins and related compounds. LXI. Isolation and structures of novel bi- and triflavanoids from the leaves of Cassia fistula L.. wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . UniChem. wikidata.org.
  15. [16] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_procyanidin-b-2_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Procyanidin B-2}}, year = {2026}, url = {https://4ort.xyz/entity/procyanidin-b-2}, note = {Accessed: 2026-05-03}}
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