(Q7701343)

3H-Bis(1)benzopyrano(3,4-b:6',5'-e)pyran-7(7aH)-one, 13,13a-dihydro-7a-hydroxy-9,10-dimethoxy-3,3-dimethyl-, (7aS-cis)-

Tephrosin (English)

4 October 2016

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(7aS)-13,13aalpha-Dihydro-7abeta-hydroxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₃H₂₂O₇

1 reference

Tephrosin (English)

4 October 2016

CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C

1 reference

Tephrosin (English)

4 October 2016

CC1(C=CC2=C(O1)C=CC3=C2O[C@@H]4COC5=CC(=C(C=C5[C@@]4(C3=O)O)OC)OC)C

1 reference

Flavonoids of Tephrosia polyphylla

Tephrosin (English)

4 October 2016

3 references

Flavonoids of Tephrosia purpurea

A new epoxyflavanone from tephrosia hamiltonii1

Tephrosia vogelii

2 references

Production of rotenoids by heterotrophic and photomixotrophic cell cultures of tephrosia vogelii

On the reported molluscicidal activity from Tephrosia vogelii leaves

Derris malaccensis

3 references

Derrisin, a new rotenoid from Derris malaccensis plain and anti-Helicobacter pylori activity of its related constituents

A new prenylated flavanone from Derris trifoliata Lour

A New Rotenoid from Derris malaccensis

Derris trifoliata

4 references

Cancer chemopreventive activity of rotenoids from Derris trifoliata

A new prenylated flavanone from Derris trifoliata Lour

Cytotoxic rotenoloids from the stems of Derris trifoliata

Two unusual rotenoid derivatives, 7a-O-methyl-12a-hydroxydeguelol and spiro-13-homo-13-oxaelliptone, from the seeds of Derris trifoliata

Erycibe expansa

1 reference

Structures of new flavonoids, erycibenins D, E, and F, and NO production inhibitors from Erycibe expansa originating in Thailand

Millettia pachycarpa

1 reference

Chemical constituents of Millettia taiwaniana: structure elucidation of five new isoflavonoids and their cancer chemopreventive activity

Mundulea sericea

2 references

Rotenoids and chalcones from Mundulea sericea that inhibit phorbol ester-induced ornithine decarboxylase activity

Rotenoids mediate potent cancer chemopreventive activity through transcriptional regulation of ornithine decarboxylase

Amorpha fruticosa

5 references

Antitumor agents, 138. Rotenoids and isoflavones as cytotoxic constitutents from Amorpha fruticosa.

Phenolic constituents of Amorpha fruticosa that inhibit NF-kappaB activation and related gene expression.

Structural Elucidation and Chemical Conversion of Amorphispironone, a Novel Spironone from Amorpha fruticosa, to Rotenoids.

Studies on inhibitors of skin tumor promotion, XII. Rotenoids from Amorpha fruticosa.

New Rotenoids inAmorpha fruticosaFruits

Derris elliptica

1 reference

A Further Rotenoid fromDerris elliptica

Millettia dura

2 references

Flavonoids from Millettia pulchra

6-Methoxycalpogonium Isoflavone A: A New Isoflavone from the Seed Pods ofMillettia dura

Millettia ferruginea

1 reference

C-prenylated isoflavones from Millettia ferruginea

Mundulea chapelieri

2 references

Cytotoxic compounds from Mundulea chapelieri from the Madagascar Rainforest.

Cytotoxic Compounds from Mundulea chapelieri from the Madagascar Rainforest

Tephrosia candida

2 references

Dimethylchromene rotenoids from Tephrosia candida

Phytochemical Investigation of Tephrosia candida: Hplc Separation of Tephrosin and 12a-Hydroxyrotenone

Tephrosia elata

2 references

Flavonoids from the Roots of Tephrosia elata

Highly variable insect control efficacy of Tephrosia vogelii chemotypes.

Tephrosia leiocarpa

1 reference

Flavanones fromTephrosia leiocarpa

Antheroporum pierrei

1 reference

Pierreiones A-D, solid tumor selective pyranoisoflavones and other cytotoxic constituents from Antheroporum pierrei

Millettia griffoniana

1 reference

Isoflavonoids from Seeds of Millettia griffoniana (Bail), 15

Sarcolobus globosus

1 reference

Rotenoids and isoflavones from Sarcolobus globosus

Derris canarensis

3 references

6-Oxo-6a,12a-dehydro-a-toxicarol, a 6-Oxodehydrorotenone from the Roots of Derris oblonga Benth

Two New Coumaronochromone Derivatives, Oblongin and Oblonginol from the Roots of Derris oblonga Benth

A new prenylated flavanone from Derris trifoliata Lour

Lonchocarpus nicou

1 reference

Lonchocarpene, a Stilbene, and Lonchocarpusone, an Isoflavone: Two New Pyranopolyphenols from Lonchocarpus nicou Roots

Deguelia urucu

1 reference

Analysis and Quantitation of Rotenoids and Flavonoids in Derris (Lonchocarpus urucu) by High-Temperature High-Resolution Gas Chromatography

Derris montana

3 references

Derrisin, a new rotenoid from Derris malaccensis plain and anti-Helicobacter pylori activity of its related constituents

A New Rotenoid from Derris malaccensis

A new prenylated flavanone from Derris trifoliata Lour

Lonchocarpus heptaphyllus

1 reference

Lonchocarpene, a Stilbene, and Lonchocarpusone, an Isoflavone: Two New Pyranopolyphenols from Lonchocarpus nicou Roots

Lonchocarpus utilis

3 references

Lonchocarpene, a Stilbene, and Lonchocarpusone, an Isoflavone: Two New Pyranopolyphenols from Lonchocarpus nicou Roots

Cubé resin insecticide: identification and biological activity of 29 rotenoid constituents

Anticancer action of cubé insecticide: correlation for rotenoid constituents between inhibition of NADH:ubiquinone oxidoreductase and induced ornithine decarboxylase activities

Derris cuneifolia

2 references

6-Oxo-6a,12a-dehydro-a-toxicarol, a 6-Oxodehydrorotenone from the Roots of Derris oblonga Benth

Two New Coumaronochromone Derivatives, Oblongin and Oblonginol from the Roots of Derris oblonga Benth

Derris

1 reference

Derrisin, a new rotenoid from Derris malaccensis plain and anti-Helicobacter pylori activity of its related constituents

Identifiers

InChI

InChI=1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1

1 reference

Tephrosin (English)

4 October 2016

2 references

Tephrosin (English)

4 October 2016

ChEBI release 2020-09-01

2 references

tephrosin (English)

4 October 2016

https://commonchemistry.cas.org/detail?cas_rn=76-80-2

9 April 2021

1 reference

Tephrosin (English)

4 October 2016

2 references

English

Tephrosin (English)

4 October 2016

InChIKey

Reaxys registry number

5661956

1 reference

tephrosin (English)

4 October 2016

mapping relation type

2 references

English

tephrosin (English)

4 October 2016

International Chemical Identifier

InChI

InChI=1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1

1 reference

splash10-014l-0219000000-0dcdfadaf47dee2ba685

TEPHROSIN (English)

4 October 2016

1 reference

0 references

DSSTox substance ID

DTXSID20878627

1 reference

InChIKey

DSSTOX compound identifier

DTXCID701016671

0 references

EC number

804-719-8

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.231.407

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 76-80-2 (English)

100.231.407

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.231.407

27 December 2018

[No public or meaningful name is available] (English)

quotation

CAS no.: 76-80-2 (English)

1 reference

Global Substance Registration System

tephrosin (English)

4 October 2016

2 references

UNII

9C081V83CC

English

TEPHROSIN (English)

4 October 2016

InChIKey

0 references

1 reference