(Q27103156)

(+)-Coclaurine (English)

5 October 2016

2 references

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₇H₁₉NO₃

1 reference

(+)-Coclaurine (English)

5 October 2016

canonical SMILES

COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O

1 reference

(+)-Coclaurine (English)

5 October 2016

isomeric SMILES

COC1=C(C=C2[C@H](NCCC2=C1)CC3=CC=C(C=C3)O)O

1 reference

Neuromuscular Blocking Action of Alkaloids from a Japanese Crude Drug “Shin-I” (Flos Magnoliae) in Frog Skeletal Muscle

(+)-Coclaurine (English)

5 October 2016

1 reference

Magnolia biondii

1 reference

Neuromuscular Blocking Action of Alkaloids from a Japanese Crude Drug “Shin-I” (Flos Magnoliae) in Frog Skeletal Muscle

Bongardia chrysogonum

1 reference

An Investigation of Bongardia chrysogonum

Cyclea peltata

2 references

Bisbenzylisoquinoline alkaloids from Cyclea barbata

Four Amidic Bisbenzylisoquinoline Alkaloids from Cyclea atjehensis

Stephania excentrica

2 references

An Alkaloid with a Novel Skeleton from the Roots ofStephania excentrica

2-N-Methylexcentricine, a New Alkaloid from Roots ofStephania excentrica

Caryomene olivascens

1 reference

Alkaloids of Caryomene olivascens (Menispermaceae). Bisbenzylisoquinoline with new structure.

Cyclea barbata

1 reference

Bisbenzylisoquinoline alkaloids from Cyclea barbata

Machilus japonica

1 reference

Three adducts of butenolide and apigenin glycoside from the leaves of Machilus japonica.

Sciadotenia eichleriana

2 references

2-Norlimacusine, Nouvelle Bisbenzylisoquinoleine Isolee de Sciadotenia eichleriana

2-Norlimacusine, Nouvelle Bisbenzylisoquinoleine Isolee de Sciadotenia eichleriana

Stephania cephalantha

2 references

Stephaoxocanine, a Novel Dihydroisoquinoline Alkaloid fromStephania cepharantha

Alkaloidal Constituents of the Tubers of Stephania cepharantha Cultivated in Japan: Structure of 3,4-Dehydrocycleanine, a New Bisbenzylisoquinoline Alkaloid.

Xylopia parviflora

1 reference

Secondary and tertiary isoquinoline alkaloids from Xylopia parviflora

Corydalis

1 reference

Alkaloids ofKorolkovia severtzovii structure of korsidine

Discaria pubescens

1 reference

Variability in Alkaloid Content of Discaria pubescens

Porcelia macrocarpa

2 references

Alkaloids From Fumaria macrocarpa

Alkaloids from Porcelia macrocarpa.

Annona cristalensis

1 reference

Annonelliptine, an alkaloid from Annona elliptica

Corydalis pseudoadunca

1 reference

Alkaloids ofCorydalis pseudoadunca

Mezilaurus synandra

1 reference

γ-Lactones from Mezilaurus synandra

Nelumbo nucifera

1 reference

Anti-HIV benzylisoquinoline alkaloids and flavonoids from the leaves of Nelumbo nucifera, and structure-activity correlations with related alkaloids

Ziziphus jujuba

1 reference

Analysis of alkaloids in the seeds ofZizyphus jujuba by high performance liquid chromatography

Identifiers

InChI

InChI=1S/C17H19NO3/c1-21-17-9-12-6-7-18-15(14(12)10-16(17)20)8-11-2-4-13(19)5-3-11/h2-5,9-10,15,18-20H,6-8H2,1H3/t15-/m1/s1

1 reference

(+)-Coclaurine (English)

5 October 2016

2 references

(+)-Coclaurine (English)

5 October 2016

ChEBI release 2020-09-01

2 references

https://commonchemistry.cas.org/detail?cas_rn=2196-60-3

(R)-coclaurine (English)

5 October 2016

6 April 2021

1 reference

(R)-Coclaurine (English)

5 October 2016

2 references

(+)-Coclaurine (English)

matched by identifier from

5 October 2016

Reaxys registry number

1546873

1 reference

(R)-coclaurine (English)

5 October 2016

ChEBI ID

27482

mapping relation type

3 references

(R)-coclaurine (English)

5 October 2016

matched by identifier from

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C17H19NO3/c1-21-17-9-12-6-7-18-15(14(12)10-16(17)20)8-11-2-4-13(19)5-3-11/h2-5,9-10,15,18-20H,6-8H2,1H3/t15-/m1/s1

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

CHEMBL256448 (English)

5 October 2016

1 reference

2 references

matched by identifier from

DSSTOX compound identifier

0 references

1 reference

(R)-coclaurine (English)

5 October 2016

1 reference