tetrandrine (Q7706612)

tetrandrine (English)

(1S,14R)-9,20,21,25-tetramethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaene

5 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

1 reference

1 reference

C₃₈H₄₂N₂O₆

1 reference

tetrandrine (English)

18 November 2016

canonical SMILES

CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC

1 reference

tetrandrine (English)

18 November 2016

isomeric SMILES

CN1CCC2=CC(=C3C=C2[C@@H]1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C[C@H]6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC

1 reference

Alkaloids of Cocculus pendulus

tetrandrine (English)

18 November 2016

3 references

The alkaloidal profile of cocculus pendulus

The alkaloidal profile of cocculus pendulus

Stephania tetrandra

7 references

A 4,5-Dioxoaporphine from the Aerial Parts of Stephania tetrandra

Analysis of tetrandrine and fangchinoline in traditional Chinese medicines by capillary electrophoresis

Separation of Alkaloids Extracted from Stephania Tetranda S. Moore by Analytical High-Speed Countercurrent Chromatography

Four New Bisbenzylisoquinoline Alkaloids from the Root of Stephania Tetrandra (Fen-Fang Ji)

Studies on Inhibitory Activity against Acetylcholinesterase of New Bisbenzylisoquinoline Alkaloid and Its Related Compounds

Induction of apoptosis in human hepatoblastoma cells by tetrandrine via caspase-dependent Bid cleavage and cytochrome c release

A New Monoquaternqry Bisbenzylisoquinoline Alkakoid from Stephania testrandra

Menispermaceae

1 reference

Tetrandrine inhibits proinflammatory cytokines, iNOS and COX-2 expression in human monocytic cells

Cyclea peltata

3 references

Isolation of Phaeanthine from Cyclea burmanni

Cytotoxic and antimalarial bisbenzylisoquinoline alkaloids from Cyclea barbata

Bisbenzylisoquinoline alkaloids from Cyclea barbata

Menispermum dauricum

1 reference

Studies on constituents of medicinal plants. XXIII. Constituents of the vines of Menispermum dauricum DC. 2.

Pachygone dasycarpa

2 references

(+)-Angchibangkine, a new type of bisbenzylisoquinoline alkaloid, and other dimers from Pachygone dasycarpa

(+)-Angchibangkine, a new type of bisbenzylisoquinoline alkaloid, and other dimers from Pachygone dasycarpa

Triclisia patens

1 reference

Additional alkaloids of Triclisia patens and Triclisia subcordata

Triclisia subcordata

2 references

Additional alkaloids of Triclisia patens and Triclisia subcordata

Additional alkaloids of Triclisia patens and Triclisia subcordata

Berberis boliviana

1 reference

Alkaloidal Content of Four Berberis Species. Structure of Berberilaurine, a New Bisbenzyltetrahydroisoquinoline

Isopyrum thalictroides

3 references

In vitro antimalarial activity of penduline, a bisbenzylisoquinoline from Isopyrum thalictroides

Alkaloids from Isopyrum thalictroides

In vitro antimalarial activity of penduline, a bisbenzylisoquinoline from Isopyrum thalictroides

Strychnopsis thouarsii

1 reference

Isoquinoline alkaloid constituents of Spirospermum penduliflorum and Strychnopsis thouarsii (Menispermaceae)

Thalictrum

1 reference

Determination of isoquinoline alkaloids inThalictrum herbal drugs by non-aqueous capillary electrophoresis

Cyclea barbata

1 reference

Bisbenzylisoquinoline alkaloids from Cyclea barbata

Stemona japonica

1 reference

Development and validation of a high-performance liquid chromatographic method for the determination of stemoninine in rat plasma after administration of Stemona tuberosa extracts

subject has role

antiviral agent

1 reference

15 March 2018

1 reference

phytogenic antineoplastic agents

15 March 2018

1 reference

15 March 2018

calcium channel blocker

1 reference

15 March 2018

immunosuppressive drug

1 reference

InChI=1S/C38H42N2O6/c1-39-15-13-25-20-32(42-4)34-22-28(25)29(39)17-23-7-10-27(11-8-23)45-33-19-24(9-12-31(33)41-3)18-30-36-26(14-16-40(30)2)21-35(43-5)37(44-6)38(36)46-34/h7-12,19-22,29-30H,13-18H2,1-6H3/t29-,30-/m0/s1

15 March 2018

Identifiers

InChI

1 reference

tetrandrine (English)

18 November 2016

2 references

tetrandrine (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

518-34-3

2 references

Global Substance Registration System

UNII

29EX23D5AJ

tetrandrine (English)

18 November 2016

https://commonchemistry.cas.org/detail?cas_rn=518-34-3

9 April 2021

0 references

2 references

tetrandrine (English)

18 November 2016

ChEBI ID

49

mapping relation type

2 references

FANCHININ (English)

18 November 2016

International Chemical Identifier

InChI

InChI=1S/C38H42N2O6/c1-39-15-13-25-20-32(42-4)34-22-28(25)29(39)17-23-7-10-27(11-8-23)45-33-19-24(9-12-31(33)41-3)18-30-36-26(14-16-40(30)2)21-35(43-5)37(44-6)38(36)46-34/h7-12,19-22,29-30H,13-18H2,1-6H3/t29-,30-/m0/s1

1 reference

FANCHININ (English)

18 November 2016

2 references

inferred from InChIKey

MSBNK-Washington_State_Univ-BML80095

1 reference

MassBank accession ID

0 references

MSBNK-Washington_State_Univ-BML80097

0 references

SPLASH

splash10-00di-0000009000-4b8068e0b260ae6ba0e6

0 references

RTECS number

XE9350000

1 reference

imported from Wikimedia project

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.615

27 December 2018

ECHA Substance Infocard ID

Tetrandrine (English)

quotation

CAS no.: 518-34-3 (English)

100.208.615

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.615

27 December 2018

Tetrandrine (English)

quotation

CAS no.: 518-34-3 (English)

subject named as

tetrandrine

1 reference

14 March 2018

1 reference

1 reference

(+)-Tetrandrine (English)

5 October 2016

1 reference

Global Substance Registration System

(+)-Tetrandrine (English)

5 October 2016

2 references

UNII

29EX23D5AJ

tetrandrine (English)

18 November 2016

VS4W77H3SD

1 reference

0 references

1 reference

(+)-Tetrandrine (English)