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linamarin

chemical compound
Class type of: carbohydrate, cyanogenic glycoside Q425157

Facts

10 properties
Instance of
type of chemical entity
Subclass of
carbohydrate, cyanogenic glycoside
Part of
linamarin synthase activity
Canonical SMILES
CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O
Chemical formula
C₁₀H₁₇NO₆
Found in taxon
Linum usitatissimum, Phaseolus lunatus, cassava, Hevea brasiliensis, Hevea benthamiana, Hevea pauciflora, Hevea spruceana, Hevea guianensis, Hevea camargoana, Acacia aroma, Lotus creticus, Passiflora adenopoda, Passiflora foetida, Passiflora lutea, Passiflora morifolia, Passiflora pendens, Trifolium repens, Linum grandiflorum, Linum narbonense, Lotus arabicus, Lotus arenarius, Lotus edulis, Lotus maroccanus, Lotus parviflorus, Lotus tenuis, Osteospermum ecklonis, Dimorphotheca jucunda, Osteospermum jucundum, Passiflora subpeltata, Turnera ulmifolia, Linum perenne, Lotus corniculatus, Trifolium occidentale, Lotus japonicus
Has characteristic
bitterness
Has part(s)
oxygen, carbon
Isomeric SMILES
CC(C)(C#N)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
Mass
247.105587 Da
🏷️ Also known as
en linamarin en Phaseolunatin ar لينامارين es Linamarina fa لینامارین fr Linamarine fr linamaroside ja C10H17NO6 ja リナマリン ru линамарин zh 亚麻苦苷
🔖 Identifiers · 25
CAS Registry Number
554-35-8
ChEBI ID
16441
ChEMBL ID
CHEMBL3039425
ChemSpider ID
10657
DSSTOX compound identifier
DTXCID5031268
DSSTox substance ID
DTXSID8052857
EC number
637-249-5
ECHA Substance Infocard ID
100.164.971
Freebase ID
/m/0288vmh
Great Russian Encyclopedia portal ID
linamarin-d12a16
HSDB ID
3507
Human Metabolome Database ID
HMDB0033699
Show all 25 identifiers +13
InChI
InChI=1S/C10H17NO6/c1-10(2,4-11)17-9-8(15)7(14)6(13)5(3-12)16-9/h5-9,12-15H,3H2,1-2H3/t5-,6-,7+,8-,9+/m1/s1
InChIKey
QLTCHMYAEJEXBT-ZEBDFXRSSA-N
KEGG ID
C01594
KNApSAcK ID
C00001446
Microsoft Academic ID (discontinued)
2777372874
Nikkaji ID
J6.462I
Probes And Drugs ID
PD001273
PubChem CID
11128
Römpp online ID
RD-12-01187
SPLASH
splash10-014i-0950000000-e342877fd4dea6a86182, splash10-0udi-0910000000-46fd8867749e9a54d5b7, splash10-0udi-0910000000-46e0422d451388f1ac6a, splash10-0006-0390000000-12125f39b36aef32a409, splash10-0006-0390000000-daf77877063e66cdc199
SureChEMBL ID
42021
UNII
H3V9RP3WLO
UniChem compound ID
1073486

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Found in taxon 31
cassava, Linum usitatissimum, Hevea brasiliensis, Trifolium repens, Lotus corniculatus, Phaseolus lunatus, Passiflora foetida, Linum narbonense +23 more
Has part(s) 2
oxygen, carbon
Subclass of 2
carbohydrate, cyanogenic glycoside
Has characteristic 1
bitterness
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Summary

linamarin is a type of chemical entity[1]. linamarin is a type of carbohydrate[2] and cyanogenic glycoside[3].

Key Facts

  • Canonical SMILES: CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O[4]
  • Chemical formula: C₁₀H₁₇NO₆[5]
  • Part of: linamarin synthase activity[6]
  • Has part(s): oxygen[7], carbon[8]
  • Found in taxon: Linum usitatissimum[9], Phaseolus lunatus[10], cassava[11], Hevea brasiliensis[12], Hevea benthamiana[13], Hevea pauciflora[14], Hevea spruceana[15], Hevea guianensis[16], Hevea camargoana[17], Acacia aroma[18], Lotus creticus[19], Passiflora adenopoda[20], Passiflora foetida[21], Passiflora lutea[22]
  • Has characteristic: bitterness[23]
  • Isomeric SMILES: CC(C)(C#N)O[C@H]1C@@HOC@@HO">[24]
  • Mass: 247.105587 dalton[25]

References

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

Direct Wikidata claims

  1. [4] ↑ . PubChem. Retrieved . wikidata.org.
  2. [5] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [3] ↑ . Chemical Diversity of Plant Cyanogenic Glycosides: An Overview of Reported Natural Products. wikidata.org.
  5. [6] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Determination of cyanogenic compounds by thin-layer chromatography. 1. A densitometric method for quantification of cyanogenic glycosides, employing enzyme preparations (.beta.-glucuronidase) from Helix pomatia and picrate-impregnated ion-exchange sheets. wikidata.org.
  9. [10] ↑ . Determination of cyanogenic compounds by thin-layer chromatography. 1. A densitometric method for quantification of cyanogenic glycosides, employing enzyme preparations (.beta.-glucuronidase) from Helix pomatia and picrate-impregnated ion-exchange sheets. wikidata.org.
  10. [11] ↑ . Determination of cyanogenic compounds by thin-layer chromatography. 1. A densitometric method for quantification of cyanogenic glycosides, employing enzyme preparations (.beta.-glucuronidase) from Helix pomatia and picrate-impregnated ion-exchange sheets. wikidata.org.
  11. [12] ↑ . Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species. wikidata.org.
  12. [13] ↑ . Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species. wikidata.org.
  13. [14] ↑ . Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species. wikidata.org.
  14. [15] ↑ . Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis. wikidata.org.
  15. [16] ↑ . Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis. wikidata.org.
  16. [17] ↑ . Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species. wikidata.org.
  17. [18] ↑ . Cyanogenic Glycosides from Four Latin American Species of Acacia. wikidata.org.
  18. [19] ↑ . A coumestan from Lotus creticus. wikidata.org.
  19. [20] ↑ . Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. wikidata.org.
  20. [21] ↑ . Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. wikidata.org.
  21. [22] ↑ . Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. wikidata.org.
  22. [23] ↑ . BitterDB. wikidata.org.
  23. [24] ↑ . PubChem. Retrieved . wikidata.org.
  24. [25] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). linamarin. Retrieved November 12, 2026, from https://4ort.xyz/entity/linamarin
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BibTeX @misc{4ortxyz_linamarin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{linamarin}}, year = {2026}, url = {https://4ort.xyz/entity/linamarin}, note = {Accessed: 2026-11-12}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 21w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of → type of chemical entity
    Has characteristic → bitterness
    Found in taxon → Linum usitatissimum, Phaseolus lunatus, cassava +1
    Subclass of → carbohydrate, cyanogenic glycoside
    + 3 other properties edited (see Wikidata diff for full list)
    "Changed [tr] labels, descriptions or aliases: QuickStatements 3.0 batch #37300"
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