(Q27101951)

Gene Ontology release 2020-05-02

Rhea release 113

methyltetrahydroprotoberberine 14-monooxygenase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

mass

354.170533±0 dalton

1 reference

(S)-N-Methylcanadine (English)

5 October 2016

chemical formula

C₂₁H₂₄NO₄⁺

1 reference

based on heuristic

inferred from SMILES

canonical SMILES

C[N+]12CCC3=CC4=C(C=C3C1CC5=C(C2)C(=C(C=C5)OC)OC)OCO4

1 reference

(S)-N-Methylcanadine (English)

5 October 2016

isomeric SMILES

C[N+]12CCC3=CC4=C(C=C3[C@@H]1CC5=C(C2)C(=C(C=C5)OC)OC)OCO4

1 reference

S-adenosyl-l-methionine: (S) -7,8,13, 14-tetrahydroberberine--n-methyltransferase, a branch point enzyme in the biosynthesis of benzophenanthridine and protopine alkaloids.

(S)-N-Methylcanadine (English)

5 October 2016

1 reference

Corydalis vaginans

1 reference

S-adenosyl-l-methionine: (S) -7,8,13, 14-tetrahydroberberine--n-methyltransferase, a branch point enzyme in the biosynthesis of benzophenanthridine and protopine alkaloids.

Fumaria officinalis

1 reference

S-adenosyl-l-methionine: (S) -7,8,13, 14-tetrahydroberberine--n-methyltransferase, a branch point enzyme in the biosynthesis of benzophenanthridine and protopine alkaloids.

Papaver somniferum

1 reference

S-adenosyl-l-methionine: (S) -7,8,13, 14-tetrahydroberberine--n-methyltransferase, a branch point enzyme in the biosynthesis of benzophenanthridine and protopine alkaloids.

Thalictrum minus

2 references

Alkaloids of the epigeal part ofThalictrum minus andTh. foetidum

Thalivarmine and Thalsivasine: Two New Bisbenzylisoquinoline Alkaloids from Thalictrum minus var. minus

Berberis soulieana

1 reference

S-adenosyl-l-methionine: (S) -7,8,13, 14-tetrahydroberberine--n-methyltransferase, a branch point enzyme in the biosynthesis of benzophenanthridine and protopine alkaloids.

Lamprocapnos spectabilis

1 reference

S-adenosyl-l-methionine: (S) -7,8,13, 14-tetrahydroberberine--n-methyltransferase, a branch point enzyme in the biosynthesis of benzophenanthridine and protopine alkaloids.

Identifiers

InChI

InChI=1S/C21H24NO4/c1-22-7-6-14-9-19-20(26-12-25-19)10-15(14)17(22)8-13-4-5-18(23-2)21(24-3)16(13)11-22/h4-5,9-10,17H,6-8,11-12H2,1-3H3/q+1/t17-,22?/m0/s1

1 reference

(S)-N-Methylcanadine (English)

IPABSWBNWMXCHM-LBOXEOMUSA-N

5 October 2016

InChIKey

2 references

(S)-N-Methylcanadine (English)

5 October 2016

ChEBI release 2020-09-01

1 reference

(7S,13aS)-9,10-dimethoxy-7-methyl-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinolin-7-ium (English)

5 October 2016

1 reference

(S)-N-Methylcanadine (English)

5 October 2016

Reaxys registry number

4160644

1 reference

(S)-N-methylcanadine (English)

5 October 2016

ChEBI ID

16512

mapping relation type

2 references

(S)-N-methylcanadine (English)

5 October 2016

ChEBI release 2019-10-02

1 reference

1 reference

(S)-N-methylcanadine (English)