(Q104394486)

English

Corynoxidine

chemical compound

In more languages

Statements

type of chemical entity

0 references

trans-N-Methylcorypalmine

1 reference

based on heuristic

inferred from SMILES

(13aS)-2,3,9,10-tetramethoxy-7-oxido-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium

1 reference

based on heuristic

inferred from SMILES

371.1732729 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

Epicorynoxidine

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(7S,13aR)-2,3,9,10-tetramethoxy-7-oxido-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₁H₂₅NO₅

0 references

canonical SMILES

[O-][N+]12CC3=C(OC)C(OC)=CC=C3CC2C4=CC(OC)=C(OC)C=C4CC1

0 references

isomeric SMILES

COc1cc2c(cc1OC)[C@@H]1Cc3ccc(OC)c(OC)c3C[N@@+]1([O-])CC2

0 references

Stephania glabra

2 references

The Alkaloids of Stephania glabra

The biosynthesis of the alkaloids of stephania glabra (ROXB.) miers

Corydalis speciosa

1 reference

Acetylcholinesterase inhibitors from the aerial parts of Corydalis speciosa

Corydalis balansae

1 reference

New tetrahydroprotoberberine N-oxide alkaloids and cytotoxic constituents of Corydalis tashiroi

Stephania rotunda

2 references

The Alkaloids of Stephania glabra

The biosynthesis of the alkaloids of stephania glabra (ROXB.) miers

Identifiers

InChI=1S/C21H25NO5/c1-24-18-6-5-13-9-17-15-11-20(26-3)19(25-2)10-14(15)7-8-22(17,23)12-16(13)21(18)27-4/h5-6,10-11,17H,7-9,12H2,1-4H3/t17-,22-/m0/s1

0 references

QYEMUDHNCZHUKC-JTSKRJEESA-N

0 references

2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

QYEMUDHNCZHUKC-JTSKRJEESA-N

UniChem compound ID

1 reference

Probes And Drugs ID

0 references

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