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rhamnose (aldehydo)

chemical compound
Class type of: rhamnose Q414109

Facts

10 properties
Instance of
type of chemical entity
Subclass of
rhamnose
Canonical SMILES
CC(C(C(C(C=O)O)O)O)O
Chemical formula
C₆H₁₂O₅
Found in taxon
Aerva lanata, Cajanus cajan, Codiaeum variegatum, Codonopsis pilosula, Daucus carota, Fagopyrum esculentum, common sunflower, Himatanthus sucuuba, Hohenbuehelia serotina, Joannesia princeps, Lantana camara, Ligusticum lucidum, Medicago lupulina, Plantago maritima, Poa huecu, Ramalina fraxinea, Siphoneugena densiflora, Thalictrum aquilegiifolium, Siraitia grosvenorii, Streptomyces griseus, Streptomyces olivaceus, Streptomyces peucetius, Allium chinense, Euterpe precatoria, Medicago sativa, Cannabis sativa, Himatanthus articulatus, Sarcomyxa serotina
Isomeric SMILES
C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O
MCN code
2940.00.13
Mass
+164.068
NCI Thesaurus ID
C68486
Stereoisomer of
(2R,3S,4S,5S)-2,3,4,5-tetrahydroxyhexanal, 6-Deoxy-L-glucose, quinovose, 6-Deoxyaltrose, D-fucose, (2S,3S,4R,5S)-2,3,4,5-tetrahydroxyhexanal, aldehydo-L-fucose, D-rhamnose
🏷️ Also known as
en rhamnose (aldehydo) en L-Rha en rhamnose en (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal cs rhamnosa cs rhamnóza cs ramnóza de L-(+)-Rhamnose es Ramnosa fa رامنوز fi ramnoosi fr Isodulcitol fr 10030-85-0 fr 3615-41-6 fr 634-74-2 fr 6-deoxy-L-mannose he רמנוז hu ramnóz it Ramnosio ja L-ラムノース
🔖 Identifiers · 37
OpenAlex ID
C2779213145
CAS Registry Number
3615-41-6
Cannabis Database ID
000139
ChEBI ID
16055
ChemSpider ID
18150
CosIng number
79550
DSSTOX compound identifier
DTXCID5022647
DSSTox substance ID
DTXSID7042647
DrugBank ID
DB02961
EC number
222-793-4
ECHA Substance Infocard ID
100.020.722
Encyclopedia of China (Second Edition) ID
230812
Show all 37 identifiers +25
Encyclopedia of China (Third Edition) ID (2026)
1yYKL
Encyclopedia of China (Third Edition) old ID (2021)
184776
Freebase ID
/m/08hvqm, /m/02kd1rr
Great Russian Encyclopedia portal ID
ramnoza-4aae94
Human Metabolome Database ID
HMDB0000849
IEDB Epitope ID
141798
InChI
InChI=1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4-,5-,6-/m0/s1
InChIKey
PNNNRSAQSRJVSB-BXKVDMCESA-N
KEGG ID
C00507
MassBank accession ID
MSBNK-MPI_for_Chemical_Ecology-CE000428, MSBNK-Osaka_Univ-OUF00444, MSBNK-Osaka_Univ-OUF00445, MSBNK-BGC_Munich-RP023411, MSBNK-GL_Sciences_Inc-GLS00164, MSBNK-GL_Sciences_Inc-GLS00165
MeSH descriptor ID
D012210
MeSH tree code
D09.254.799
Microsoft Academic ID (discontinued)
2779213145
NSC number
2056
Nikkaji ID
J8.185J
PDB ligand ID
RNS
PDB structure ID
3ITT, 3M0H, 3M0V, 3M0Y, 2I56, 4GJI, 1DE6, 1X8D
Probes And Drugs ID
PD059745
PubChem CID
19233
Reaxys registry number
1723326
RxNorm CUI
1872246
SPLASH
splash10-014i-0920000000-845777ce5ccb02564dd4, splash10-000i-0900000000-c17a9df600308d9b31be, splash10-014i-0910000000-a3998948f1f154365fea, splash10-014i-0900000000-09ff33efc7ead61776ac
SureChEMBL ID
25050
UNII
QN34XC755A
UniChem compound ID
643864

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

🔗 Connections
Found in taxon 23
common sunflower, Fagopyrum esculentum, Medicago sativa, Cannabis sativa, Daucus carota, Cajanus cajan, Lantana camara, Medicago lupulina +15 more
Belongs to 1
verbascoside
Press Enter · cited answer in seconds

Summary

rhamnose (aldehydo) is a type of chemical entity[1]. rhamnose (aldehydo) is a type of rhamnose[2].

Key Facts

  • Canonical SMILES: CC(C(C(C(C=O)O)O)O)O[3]
  • Chemical formula: C₆H₁₂O₅[4]
  • Found in taxon: Aerva lanata[5], Cajanus cajan[6], Codiaeum variegatum[7], Codonopsis pilosula[8], Daucus carota[9], Fagopyrum esculentum[10], common sunflower[11], Himatanthus sucuuba[12], Hohenbuehelia serotina[13], Joannesia princeps[14], Lantana camara[15], Ligusticum lucidum[16], Medicago lupulina[17], Plantago maritima[18]
  • NCI Thesaurus ID: C68486[19]
  • MCN code: 2940.00.13[20]
  • Isomeric SMILES: CC@HC@HC@@HC@@HC=OC@HC@HC@@HC@@HC=O">[21]
  • Mass: 164.068 dalton[22]
  • Stereoisomer of: (2R,3S,4S,5S)-2,3,4,5-tetrahydroxyhexanal[23], 6-Deoxy-L-glucose[24], quinovose[25], 6-Deoxyaltrose[26], D-fucose[27], (2S,3S,4R,5S)-2,3,4,5-tetrahydroxyhexanal[28], aldehydo-L-fucose[29], D-rhamnose[30]

References

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

Direct Wikidata claims

  1. [3] ↑ . PubChem. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [5] ↑ . Carbohydrates of Aerva lanata. wikidata.org.
  5. [6] ↑ . Analysis of phenolic acids and carbohydrates in pigeon pea (Cajanus cajan) plant. wikidata.org.
  6. [7] ↑ . Local plants as potential sources of tannins in Egypt, part. IV (Aceraceae to Flacourtiaceae). wikidata.org.
  7. [8] ↑ . Development and application of a capillary electrophoretic method for the composition analysis of a typical heteropolysaccharide from Codonopsis pilosula NANNF.. wikidata.org.
  8. [9] ↑ . Structural features of cell-wall polysaccharides of the carrot Daucus carota. wikidata.org.
  9. [10] ↑ . Biosynthesis of l-rhamnose from d-glucose in buckwheat. wikidata.org.
  10. [11] ↑ . Sunflower carbohydrates. wikidata.org.
  11. [12] ↑ . Contribution to the study of Himatanthus sucuuba: latex macromolecule, microelements and carbohydrates. wikidata.org.
  12. [13] ↑ . Chemical Constituents of a Heat-dried Chinese Mushroom,Hohenbuehelia serotina. wikidata.org.
  13. [14] ↑ . Joannesialactone and other compounds from Joannesia princeps. wikidata.org.
  14. [15] ↑ . PHYTOCHEMICAL STUDY OF LANTANA CAMARA I. wikidata.org.
  15. [16] ↑ . Chemical constituents from fruits of Ligustrum lucidum. wikidata.org.
  16. [17] ↑ . Studies on Medicago lupulina saponins. 2. Isolation, chemical characterization and biological activity of saponins from M. lupulina tops. wikidata.org.
  17. [18] ↑ . Osmoregulation in halophytic higher plants: a comparative study of soluble carbohydrates, polyols, betaines and free proline.. wikidata.org.
  18. [19] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  21. [22] ↑ . PubChem. Retrieved . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.
  26. [27] ↑ . wikidata.org.
  27. [28] ↑ . wikidata.org.
  28. [29] ↑ . wikidata.org.
  29. [30] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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.

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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. 17w ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    Encyclopedia of China (Third Edition) ID (2026) → 1yYKL
    "Changed the item: QuickStatements 3.0 batch #40849: ZGBK ID"
  2. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → (2R,3S,4S,5S)-2,3,4,5-tetrahydroxyhexanal, 6-Deoxy-L-glucose, quinovose +1
    Instance of → type of chemical entity
    Found in taxon → Aerva lanata, Cajanus cajan, Codiaeum variegatum +1
    Subclass of → rhamnose
    + 1 other property edited (see Wikidata diff for full list)
    "Changed [tr] labels, descriptions or aliases: QuickStatements 3.0 batch #37300"
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