hopane triterpenoid
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hopane triterpenoid
Summary
hopane triterpenoid is a structural class of chemical entities[1]. It draws 27 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #211 of 1,029).[2]
Key Facts
- hopane triterpenoid's instance of is recorded as structural class of chemical entities[3].
- hopane triterpenoid's subclass of is recorded as triterpenoid[4].
- hopane triterpenoid's part of is recorded as hopanoid catabolic process[5].
- hopane triterpenoid's part of is recorded as hopanoid metabolic process[6].
- hopane triterpenoid's part of is recorded as hopanoid biosynthetic process[7].
- hopane triterpenoid's Commons category is recorded as Hopanoids[8].
- hopane triterpenoid's Freebase ID is recorded as /m/0732c7[9].
- hopane triterpenoid's KEGG ID is recorded as C06084[10].
- hopane triterpenoid's ChEBI ID is recorded as 51963[11].
- hopane triterpenoid's LIPID MAPS ID is recorded as LMPR04[12].
- hopane triterpenoid's Microsoft Academic ID is recorded as 167195282[13].
- hopane triterpenoid's SMARTS notation is recorded as [$(C);!$(C(~C)~C)]~$(C);!$(C(~C)(~C)(~C)~C)~[$(C);!$(C(~C)(~C)(~C)~C)]1~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C2([$(C);!$(C(~C)~C)])[$(C);!$(C(~C)(~C)(~C)~C)]3~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)][$(C);!$(C(~C)(~C)(~C)~C)]4C5([$(C);!$(C(~C)~C)])[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C([$(C);!$(C(~C)~C)])([$(C);!$(C(~C)~C)])[$(C);!$(C(~C)(~C)(~C)~C)]5~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C([$(C);!$(C(~C)~C)])4C([$(C);!$(C(~C)~C)])3[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)(~C)~C)]2~1$(C);!$(C(~C)(~C)(~C)~C)~[$(C);!$(C(~C)(~C)(~C)~C)]1~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C2([$(C);!$(C">[14].
- hopane triterpenoid's SMARTS notation is recorded as [$(C);!$(C(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~$(C);!$(C(~C)(~C)(~C)~C)~[$(C);!$(C(~C)(~C)(~C)~C)]1~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C2([$(C);!$(C(~C)~C)])[$(C);!$(C(~C)(~C)(~C)~C)]3[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)(~C)~C)]4C5([$(C);!$(C(~C)~C)])[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C([$(C);!$(C(~C)~C)])([$(C);!$(C(~C)~C)])[$(C);!$(C(~C)(~C)(~C)~C)]5~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]C([$(C);!$(C(~C)~C)])4C([$(C);!$(C(~C)~C)])3[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)(~C)~C)]2~1[15].
- hopane triterpenoid's OpenAlex ID is recorded as C167195282[16].
Why It Matters
hopane triterpenoid draws 27 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #211 of 1,029).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[17] It is known by 5 alternative names across languages and contexts.[18]