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laudanosine

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composto chimico

Risorse esterne

identificativo Freebase
identificativo Microsoft Academic
identificativo PubChem
identificativo DSSTOX di un composto chimico
identificativo composto UniChem
identificativo KEGG
NSC number
identificativo ChEMBL
identificativo Gran Enciclopèdia Catalana
InChIKey
identificativo Gran Enciclopèdia Catalana (obsoleto)
InChI
Römpp online ID
SureChEMBL ID
identificativo KNApSAcK
identificativo ECHA InfoCard
identificativo ChEBI
6389[6][10]

tipo di relazione: corrispondenza esatta

identificativo ChemSpider
numero CE
220-253-2[12]
UMLS CUI
numero CAS
identificativo DSSTOX sostanza
identificativo MeSH
Probes And Drugs ID
identificativo UNII

no tipo 'e

type of chemical entity

sottoclasse di

isoquinoline alkaloid

struttura chimica

massa

357,194 unità e' massa atomeca[16]

stereoisomero di

(R)-laudanosine[8][17]

formula chimica

C₂₁H₂₇NO₄[2]

SMILES canonico

CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC[2]

SMILES isomerico

CN1CCC2=CC(=C(C=C2[C@@H]1CC3=CC(=C(C=C3)OC)OC)OC)OC[2]

trovato nella tassonomia de

Hubera cerasoides[18]
Berberis heteropoda[19]
Berberis nummularia[20]
Cissampelos pareira[21]
Guatteria amplifolia[22]
Papaver macrostomum[23]
Papaver setigerum[24]
Croton gratissimus[25]
Hazomalania voyronii[26]
Papaver somniferum[27]

ruolo del soggetto

agente del sistema nervoso centrale[28]

categoria su Commons

Laudanosine

Riferimento

  1. Freebase Data Dumps, 28 ott 2013
  2. 2,0 2,1 2,2 2,3 2,4 2,5 PubChem, 20 Nuv 2016, Lengua ngrese, 73397, N-Methyltetrahydropapaverine
  3. 3,0 3,1 3,2 3,3 KGPAYJZAMGEDIQ-KRWDZBQOSA-N, InChIKey
  4. UniChem
  5. 5,0 5,1 5,2 ChEBI, 5 ott 2016, Lengua ngrese, Laudanosine, 6389
  6. 6,0 6,1 ChEMBL, 20 Nuv 2016, Lengua ngrese, CHEMBL519894, CHEMBL519894
  7. ChEBI release 2020-09-01
  8. 8,0 8,1 inferred from InChIKey
  9. ECHA Substance Infocard database, 27 dic 2018, 100.018.412, Laudanosine, CAS no.: 2688-77-9
  10. International Chemical Identifier, InChI=1S/C21H27NO4/c1-22-9-8-15-12-20(25-4)21(26-5)13-16(15)17(22)10-14-6-7-18(23-2)19(11-14)24-3/h6-7,11-13,17H,8-10H2,1-5H3/t17-/m0/s1
  11. ChemSpider, 20 Nuv 2016, Lengua ngrese, 66114, Laudanosine
  12. 12,0 12,1 12,2 Global Substance Registration System, 20 Nuv 2016, Lengua ngrese, laudanosine, DA7R5WVN48
  13. UMLS 2023, 25 Maj 2023, inferred by common MeSH mappings on source and on Wikidata
  14. CAS Common Chemistry, 8 Abb 2021, KGPAYJZAMGEDIQ-KRWDZBQOSA-N, https://commonchemistry.cas.org/detail?cas_rn=2688-77-9
  15. Medical Subject Headings, 14 Màr 2018, C001522
  16. PubChem, 5 ott 2016, Lengua ngrese, 73397, N-Methyltetrahydropapaverine
  17. inferred from InChI
  18. Bioactive constituents of the roots of Polyalthia cerasoides
  19. Berberis alkaloids. XVII. Investigation of the alkaloids of Berberis heteropoda
  20. Berberis alkaloids. XXIV. Structure of bernumine
  21. Alkaloids of Cissampelos pareira
  22. Aporphine alkaloids from Guatteria spp. with leishmanicidal activity
  23. Antimicrobial Activity and Phytochemical Studies on Turkish Samples ofPapaver macrostomum.
  24. Alkaloids from Papaver setigerum DC.
  25. HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
  26. Alkaloids of Hernandia voyronii: chloroquine-potentiating activity and structure elucidation of herveline D.
  27. Separation of eight alkaloids and meconic acid and quantitation of five principal alkaloids in gum opium by gradient reversed-phase high-performance liquid chromatography
  28. Medical Subject Headings, 15 Màr 2018, C001522