(Q27144976)

inferred from SMILES

mass

414.131468±0 dalton

1 reference

beta-Peltatin (English)

(5aS,8aS,9R)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one

8 October 2016

stereoisomer of

2 references

inferred from InChIKey

(5aR,8aS,9R)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-isobenzofuro[6,5-f][1,3]benzodioxol-8-one

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₂H₂₂O₈

1 reference

beta-Peltatin (English)

20 November 2016

canonical SMILES

COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O

1 reference

beta-Peltatin (English)

20 November 2016

isomeric SMILES

COC1=CC(=CC(=C1OC)OC)[C@H]2[C@@H]3[C@@H](CC4=C(C5=C(C=C24)OCO5)O)COC3=O

1 reference

Potential anticancer agents II: antitumor and cytotoxic lignans from Linum album (Linaceae)

beta-Peltatin (English)

20 November 2016

2 references

Accumulation of podophyllotoxin and related lignans in cell suspension cultures of linum album

Linum catharticum

1 reference

Arytetralin lignans from Linum catharticum L.

Tetraclinis articulata

1 reference

Diterpenoids from Tetraclinis articulata that inhibit various human leukocyte functions

Bridelia ferruginea

1 reference

A New Podophyllotoxin Derivative fromBridelia ferruginea

Diphylleia cymosa

1 reference

Tumour-inhibitory aryltetralin lignans in Podophyllum versipelle, Diphylleia cymosa and Diphylleia grayi

Diphylleia grayi

1 reference

Tumour-inhibitory aryltetralin lignans in Podophyllum versipelle, Diphylleia cymosa and Diphylleia grayi

Eriope macrostachya

1 reference

Alpha- and beta-peltatin from Eriope macrostachya

Hugonia tomentosa

1 reference

Lignans from Hugonia tomentosa

Libocedrus bidwillii

1 reference

Antitumour lignans and cytotoxic resin acids from a New Zealand gymnosperm, Libocedrus plumosa

Linum arboreum

1 reference

Linum austriacum

1 reference

Linum boissieri

1 reference

Linum campanulatum

1 reference

Linum capitatum

3 references

Aryltetralin lignans from Linum flavum and Linum capitatum

Aryltetralin lignans from Linum flavum and Linum capitatum

Linum cariense

1 reference

Linum corymbulosum

1 reference

Linum elegans

1 reference

Linum hirsutum

1 reference

Linum lewisii

1 reference

Linum monogynum

1 reference

Linum mucronatum

1 reference

Linum nodiflorum

1 reference

Linum pamphylicum

1 reference

Linum tauricum

1 reference

Linum thracicum

1 reference

Linum viscosum

1 reference

Podophyllum hexandrum

4 references

Quantitative determination of podophyllotoxin and related compounds inpodophyllum species by reverse phase high performance liquid chromatography

Biosynthesis of the lignans α- and β-peltatin

Aryltetralin lignans from Podophyllum hexandrum and Podophyllum peltatum

Aryltetralin lignans from Podophyllum hexandrum and Podophyllum peltatum

Podophyllum versipelle

1 reference

Tumour-inhibitory aryltetralin lignans in Podophyllum versipelle, Diphylleia cymosa and Diphylleia grayi

Pulsatilla chinensis

1 reference

Triterpene saponins and lignans from the roots of Pulsatilla chinensis and their cytotoxic activity against HL-60 cells.

Eriope latifolia

1 reference

Podophyllotoxin and other aryltetralin lignans from Eriope latifolia and Eriope blanchetii

Thujopsis dolabrata

1 reference

A diterpene glycoside and lignans from seed of Thujopsis dolabrata

Thujopsis dolabrata var. hondae

1 reference

A diterpene glycoside and lignans from seed of Thujopsis dolabrata

Juniperus phoenicea

1 reference

Plant Anticancer Agents. X. Lignans From Juniperus phoenicea

Juniperus sabina

2 references

Acetylated lignans from Juniperus sabina

Lignans from Juniperus sabina

Juniperus thurifera

1 reference

Lignans from Juniperus thurifera

Calocedrus decurrens

1 reference

Discovery and development of anticancer agents from plants

Bursera simaruba

1 reference

Phenolic compounds from Bursera simaruba Sarg. bark: phytochemical investigation and quantitative analysis by tandem mass spectrometry

Bursera permollis

1 reference

Cytotoxic constituents of Bursera permollis

Podophyllum peltatum

10 references

An Investigation of the Antiviral Activity of Podophyllum peltatum

Evaluation of Podophyllum peltatum accessions for podophyllotoxin production

Analysis of aryltetrahydronaphthalene lignans and their glucoside conjugates in podophyllin resin by high-performance liquid chromatography

Quantitative determination of podophyllotoxin and related compounds inpodophyllum species by reverse phase high performance liquid chromatography

The American mayapple revisited—podophyllum peltatum—still a potential cash crop?

Quantitation of Aryltetralin Lignans in Plant Parts and among Different Populations ofPodophyllumpeltatumby Reversed-Phase High-Performance Liquid Chromatography

Immunosuppressive cyclolignans

Search for New Drugs of Plant Origin

Biosynthesis of the lignans α- and β-peltatin

Matairesinol as precursor of Podophyllum lignans

Linum flavum

2 references

Formation of beta-peltatin-A methyl ether and coniferin by root cultures of Linum flavum.

Dysosma versipellis

1 reference

Tumour-inhibitory aryltetralin lignans in Podophyllum versipelle, Diphylleia cymosa and Diphylleia grayi

Condea verticillata

1 reference

Chemical Constituents of Hyptis suaveolens. Part I. Spectral and Biological Studies on a Triterpene Acid

catalog

CAS COVID-19 Anti-Viral Candidate Compounds

0 references

Identifiers

InChI

InChI=1S/C22H22O8/c1-25-14-5-10(6-15(26-2)20(14)27-3)17-12-7-16-21(30-9-29-16)19(23)13(12)4-11-8-28-22(24)18(11)17/h5-7,11,17-18,23H,4,8-9H2,1-3H3/t11-,17+,18-/m0/s1

1 reference

beta-Peltatin (English)

HLBPOYVRLSXWJJ-PDSMFRHLSA-N

20 November 2016

InChIKey

2 references

beta-Peltatin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

518-29-6

2 references

Global Substance Registration System

UNII

3U9W61G72Y

https://commonchemistry.cas.org/detail?cas_rn=518-29-6

β-peltatin (English)

20 November 2016

6 April 2021

InChIKey

HLBPOYVRLSXWJJ-PDSMFRHLSA-N

1 reference

b-Peltatin (English)

20 November 2016

1 reference

beta-Peltatin (English)

20 November 2016

Reaxys registry number

99483

1 reference

beta-peltatin (English)

8 October 2016

ChEBI ID

74867

mapping relation type

1 reference

BETA-PELTATIN A (English)

20 November 2016

1 reference

MSBNK-Washington_State_Univ-BML82435

BETA-PELTATIN A (English)

20 November 2016

1 reference

MassBank accession ID

0 references

MSBNK-Washington_State_Univ-BML82436

0 references

MSBNK-Washington_State_Univ-BML82437

0 references

MSBNK-Washington_State_Univ-BML82438

0 references

SPLASH

splash10-03di-0000900000-d8a2e92eaed3ce8bd502

0 references

splash10-014i-0000900000-312199ed580050df07ba

0 references

splash10-001i-0009000000-2dbf5736666bf3393084

0 references

splash10-001i-0009000000-f69c0a75d4302b90c66b

0 references

splash10-03di-0019800000-9ba56f7a45122ccd789f

0 references

splash10-03di-0017900000-17e9a61f7638d42b7b9a

0 references

splash10-014i-0001900000-bba3e1a04c58a970873f

0 references

splash10-014i-0002900000-5cee8234490d5a3269b9

0 references

DSSTox substance ID

DTXSID10199732

1 reference

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

DSSTOX compound identifier

0 references

0 references

0 references

AICS Chemical ID (BEING DELETED)

0 references

1 reference

Global Substance Registration System

UNII

3U9W61G72Y