(Q27102599)

Gene Ontology release 2020-05-02

Rhea release 113

(S)-scoulerine 9-O-methyltransferase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

(S)-canadine synthase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

(-)-Isocorypalmine.svg
700 × 470; 17 KB

0 references

mass

341.162708±0 dalton

1 reference

483-34-1 (English)

5 October 2016

2 references

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₀H₂₃NO₄

1 reference

483-34-1 (English)

20 November 2016

COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC

1 reference

483-34-1 (English)

20 November 2016

COC1=C(C2=C(C[C@H]3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC

1 reference

Anti-thrombic action of methanol extract and alkaloidal components from Corydalis tuber

483-34-1 (English)

20 November 2016

4 references

Quantitative analysis of tertiary and quaternary alkaloids in Corydalis Tuber by ion-pair high-performance liquid chromatography and its application to an oriental pharmaceutical preparation

Characterization of aromatase binding agents from the dichloromethane extract of Corydalis yanhusuo using ultrafiltration and liquid chromatography tandem mass spectrometry.

Influence of vinegar and wine processing on the alkaloid content and composition of the traditional Chinese medicine Corydalis Rhizoma (Yanhusuo).

Glaucium fimbrilligerum

2 references

Alkaloids of Glaucium fimbrilligerum

Alkaloids ofGlaucium fimbrilligerum. II

Liriodendron tulipifera

2 references

Alkaloids of Liriodendron tulipifera

N-methyllaurotetanine and isocorypalmine from Liriodendron tulipifera

Annickia chlorantha

1 reference

Protoberberine alkaloids from the bark of Enantia chlorantha

Corydalis

1 reference

Alkaloids from Corydalis Incisa

Corydalis nobilis

1 reference

Alkaloids from Corydalis nobilis (L.) PERS. and C. intermedia (L.) MÉRAT

Corydalis solida

2 references

Alkaloids from Corydalis solida (L.) SW. mass spectrometry of quaternary benzylisoquinoline alkaloids

Alkaloids from Corydalis solida (L.) SW. mass spectrometry of quaternary benzylisoquinoline alkaloids

Hydrastis canadensis

1 reference

Antimicrobial constituents from goldenseal (the Rhizomes of Hydrastis canadensis) against selected oral pathogens.

Thalictrum dioicum

1 reference

Alkaloids of Thalictrum. X. Two new alkaloids from T. minus var. adiantifolium: noroxyhydrastinine and thalifoline

Bocconia frutescens

1 reference

Alkaloids from Bocconia frutescens L.

Corydalis chaerophylla

1 reference

New alkaloids from Corydalis species

Pseudofumaria alba

1 reference

THE ALKALOIDS OF FUMARIACEOUS PLANTS: XXI. CORYDALIS LUTEA (L.) DC.

Corydalis ophiocarpa

1 reference

Formation of alkaloids in Corydalis ophiocarpa callus culture

Corydalis heterocarpa

1 reference

THE ALKALOIDS OF FUMARIACEOUS PLANTS: XXXV. CORYDALIS PLATYCARPA MAKINO

Corydalis saxicola

1 reference

Tetrahydroprotoberberine alkaloids from Corydalis saxicola

Corydalis turtschaninovii

1 reference

New cytotoxic tetrahydroprotoberberine-aporphine dimeric and aporphine alkaloids from Corydalis turtschaninovii

Fibraurea recisa

1 reference

Antifungal alkaloids from the fresh rattan stem of Fibraurea recisa Pierre

Ceratocapnos heterocarpa

1 reference

THE ALKALOIDS OF FUMARIACEOUS PLANTS: XXXV. CORYDALIS PLATYCARPA MAKINO

Corydalis cava

1 reference

Positive Cooperation of Protoberberine Type 2 Alkaloids fromCorydalis cavaon the GABAABinding Site

Pseudofumaria lutea

1 reference

Crabbine, an aporphine alkaloid from Corydalis lutea

Thalictrum flavum

1 reference

Structural and Functional Studies of Pavine N-Methyltransferase from Thalictrum flavum Reveal Novel Insights into Substrate Recognition and Catalytic Mechanism

Identifiers

InChI

InChI=1S/C20H23NO4/c1-23-18-5-4-12-8-16-14-10-17(22)19(24-2)9-13(14)6-7-21(16)11-15(12)20(18)25-3/h4-5,9-10,16,22H,6-8,11H2,1-3H3/t16-/m0/s1

1 reference

483-34-1 (English)

20 November 2016

2 references

483-34-1 (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

483-34-1

2 references

Global Substance Registration System

UNII

MX470OL19D

(-)-isocorypalmine (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=483-34-1

9 April 2021

1 reference

(13aS)-3,9,10-Trimethoxy-5,8,13,13a-tetrahydro-6H-isoquinolino[3,2-a]isoquinolin-2-ol (English)

20 November 2016

2 references

483-34-1 (English)

20 November 2016

Reaxys registry number

4717587

1 reference

(S)-tetrahydrocolumbamine (English)

5 October 2016

ChEBI ID

17772

mapping relation type

2 references

CHEMBL2334891 (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C20H23NO4/c1-23-18-5-4-12-8-16-14-10-17(22)19(24-2)9-13(14)6-7-21(16)11-15(12)20(18)25-3/h4-5,9-10,16,22H,6-8,11H2,1-3H3/t16-/m0/s1

1 reference

CHEMBL2334891 (English)

20 November 2016

2 references

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

DTXCID601391759

0 references

KNApSAcK ID

C00025632

reason for deprecated rank

cannot be confirmed by other sources

1 reference

Global Substance Registration System

(S)-tetrahydrocolumbamine (English)

5 October 2016

2 references

UNII

MX470OL19D

(-)-isocorypalmine (English)

20 November 2016