apocarotenoid

class of compounds

ChemicalSubstance structural_class_of_chemical_entities Q4489785

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apocarotenoid

Summary

apocarotenoid is a structural class of chemical entities^[1]. apocarotenoid draws 7 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #235 of 1,029).^[2]

Key Facts

apocarotenoid's instance of is recorded as structural class of chemical entities^[3].
apocarotenoid's subclass of is recorded as tetraterpenoid^[4].
apocarotenoid's Freebase ID is recorded as /m/05ms988^[5].
apocarotenoid's topic's main category is recorded as Category:Apocarotenoids^[6].
apocarotenoid's Microsoft Academic ID is recorded as 2775892496^[7].
apocarotenoid's SMARTS notation is recorded as [$(C);!$(C(~C)~C)]C1([$(C);!$(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)]~$(C);!$(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)~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)(~C)~C)~[$">[8]}.
apocarotenoid's SMARTS notation is recorded as [$(C);!$(C(~C)~C)]C1([$(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);!$(C(~C)(~C)~C)]~$(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);!$(C(~C)(~C)~C)]~[$(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);!$(C(~C)(~C)(~C)~C)~[$">[9]}.
apocarotenoid's SMARTS notation is recorded as [$(C);!$(C(~C)~C)]C1([$(C);!$(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)]~$(C);!$(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)~C)]~[$(C);!$(C(~C)(~C)~C)]~$(C);!$(C(~C)(~C)(~C)~C)~[$(C);!$(C(~C)~C)]^{$(C);!$(C(~C)(~C)(~C)~C)~[$">[10]}.
apocarotenoid's SMARTS notation is recorded as [$(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);!$(C(~C)(~C)(~C)~C)~[$(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);!$(C(~C)(~C)~C)]~$(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)]~">[11]}.

Why It Matters

apocarotenoid draws 7 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #235 of 1,029).^[2] apocarotenoid has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.^[12]

⭐ Popularity Graph

1/100 long tail

🌐 Wiki Languages

7 / 423 langs

📈 Wikipedia Views · last 19h

18/mo 26/yr

🔗 Readers Also Explored · clickstream

carotenoid

📊 Google Search Volume

no search data yet

Quick Facts

Instance of structural class of chemical entities

Subclass of tetraterpenoid

Properties

Smarts notation [$(C);!$(C(~C)~C)]C1([$(C);!$(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)]~[$(C);!$(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)]~[$(C);!$(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(~C)(~C)(~C)~C)](~[$(C);!$(C(~C)~C)])~[$(C);!$(C(~C)~C)], [$(C);!$(C(~C)~C)]C1([$(C);!$(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)]~[$(C);!$(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)]~[$(C);!$(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)~C)]C1([$(C);!$(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)]~[$(C);!$(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)]~[$(C);!$(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)~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)]~[$(C);!$(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)]~[$(C);!$(C(~C)(~C)(~C)~C)](~[$(C);!$(C(~C)~C)])~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)(~C)~C)]~[$(C);!$(C(~C)~C)]

Topic's main category Category:Apocarotenoids

External References (2)

Freebase id /m/05ms988

Microsoft academic id (discontinued) 2775892496

🌐 Available in 5 languages

enApocarotenoid deApocarotinoide frApocaroténoïde jaアポカロテノイド plApokarotenoidy

🔗 Connections

Subtypes 5

bixin, peridinin, apocarotenal, Food orange 7, trans-norbixin

Topic's main category 1

Category:Apocarotenoids

← Category's main topic 1

Category:Apocarotenoids

References

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

Direct Wikidata claims

Class ancestry

[1] ↑ apocarotenoid is an instance of structural class of chemical entities (Q47154513) [P31, primary]. Wikidata. wikidata.org.

Aggregate / graph-position facts

[2] ↑ apocarotenoid draws 7 Wikipedia views per month (structural_class_of_chemical_entities category, ranking #235 of 1,029).. Wikimedia Foundation. dumps.wikimedia.org.
[12] ↑ apocarotenoid has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.. Wikidata sitelinks. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). apocarotenoid. Retrieved May 3, 2026, from https://4ort.xyz/entity/apocarotenoid

MLA “apocarotenoid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/apocarotenoid.

BibTeX

@misc{4ortxyz_apocarotenoid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{apocarotenoid}}, year = {2026}, url = {https://4ort.xyz/entity/apocarotenoid}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): apocarotenoid — https://4ort.xyz/entity/apocarotenoid (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/apocarotenoid · Last refreshed: May 3, 2026