leucoanthocyanidin

Summary

leucoanthocyanidin is a structural class of chemical entities^[1]. leucoanthocyanidin draws 11 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #236 of 1,029).^[2]

Key Facts

• leucoanthocyanidin's image is recorded as Flavan-3,4-diol.svg^[3].
• leucoanthocyanidin's instance of is recorded as structural class of chemical entities^[4].
• leucoanthocyanidin's canonical SMILES is recorded as OC1C(O)c2c([])c([])c([])c([])c2OC1c1c([])c([])c([])c([])c1[*]^[5].
• leucoanthocyanidin's subclass of is recorded as flavan-3-ol^[6].
• leucoanthocyanidin's subclass of is recorded as flavan-4-ol^[7].
• leucoanthocyanidin's part of is recorded as leucoanthocyanidin metabolic process^[8].
• leucoanthocyanidin's part of is recorded as leucoanthocyanidin biosynthetic process^[9].
• leucoanthocyanidin's Commons category is recorded as Leucoanthocyanidins^[10].
• leucoanthocyanidin's Freebase ID is recorded as /m/07kbgcl^[11].
• leucoanthocyanidin's ChEBI ID is recorded as 60835^[12].
• leucoanthocyanidin's topic's main category is recorded as Category:Leucoanthocyanidins^[13].
• leucoanthocyanidin's Microsoft Academic ID is recorded as 2777143092^[14].
• leucoanthocyanidin's SMARTS notation is recorded as [#8]-[#6]-1-#6-c2c(-)c(-)c(-)c(-)c2-[#8]-[#6]-1-c1c(-)c(-)c(-)c(-)c1-*^{#6-c2c(-*)c(-*)c(-*)c(-*)c2-[#8]-[#6]-1-c1c(-*)c(-*)c(-*)c(-*)c1-*">[15]}.
• leucoanthocyanidin's CXSMILES is recorded as OC1C(O)c2c([])c([])c([])c([])c2OC1c1c([])c([])c([])c([])c1[*] |$;;;;;;R;;R;;R;;R;;;;;;R;;R;;R;;R;;R$|^[16].

Why It Matters

leucoanthocyanidin draws 11 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #236 of 1,029).^[2] leucoanthocyanidin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.^[17] leucoanthocyanidin is known by 9 alternative names across languages and contexts.^[18]