(Q27089355)

English

hinokinin

chemical compound

(3R,4R)-3,4-bis(1,3-benzodioxol-5-ylmethyl)dihydrofuran-2(3H)-one
(3R-trans)-3,4-bis(1,3-benzodioxol-5-ylmethyl)dihydrofuran-2(3H)-one
(-)-hinokinin
Hinokinin

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type of chemical entity

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subclass of

chemical compound

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chemical structure

Hinokinin.png
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mass

354.110338 dalton

1 reference

language of work or name

Hinokinin (English)

4 October 2016

2 references

inferred from InChIKey

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C₂₀H₁₈O₆

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language of work or name

Hinokinin (English)

4 October 2016

C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5

1 reference

language of work or name

Hinokinin (English)

4 October 2016

C1[C@@H]([C@H](C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5

1 reference

language of work or name

Hinokinin (English)

4 October 2016

2 references

An N-methyl aristolactam and an oxygenated cyclohexane derivative from Piper ribesioides

stated in

A New Linalool Derivative and Other Constituents fromPiper ribesoides

Juniperus thurifera

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stated in

Lignans from Juniperus thurifera

Hypenia salzmannii

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stated in

(−)-Salzol, an isopimarane diterpene, and a chalcone from Hyptis salzmanii

Aristolochia triangularis

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stated in

Terpenes from Aristolochia triangularis

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Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

West African Pepper

1 reference

stated in

Lignans of Piper clusii☆

Calocedrus formosana

1 reference

stated in

Lignans from wood of Calocedrus formosana

Piper cubeba

4 references

stated in

Antileishmanial amides and lignans from Piper cubeba and Piper retrofractum

stated in

Potent CYP3A4 Inhibitory Constituents of Piper cubeba

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Lignans from Piper cubeba

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Potent CYP3A4 inhibitory constituents of Piper cubeba

Virola elongata

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stated in

Lignoids and arylalkanones from fruits of Virola elongata

Virola venosa

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Flavones and lignans in flowers, fruits and seedlings ofVirola venosa

Hypoestes purpurea

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stated in

Furanolabdane diterpenes from Hypoestes purpurea

Bursera simaruba

1 reference

stated in

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

Aristolochia constricta

1 reference

stated in

Chemical constituents of Aristolochia constricta: antispasmodic effects of its constituents in guinea-pig ileum and isolation of a diterpeno-lignan hybrid

Aristolochia cymbifera

2 references

stated in

Epi-populifolic acid from Aristolochia cymbifera

stated in

Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

Phyfnnvik eyyfn

2 references

stated in

Isolintetralin: A New Lignan from Phyllanthus niruri

stated in

Screening of 25 compounds isolated from Phyllanthus species for anti‐human hepatitis B virus in vitro

Zanthoxylum simulans

1 reference

stated in

Chemical and bioactive constituents from Zanthoxylum simulans

Aristolochia pubescens

2 references

stated in

Diterpene esters of aristolochic acids from Aristolochia pubescens.

stated in

Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

Chamaecyparis obtusa var. formosana

1 reference

stated in

New lignans from the heartwood of Chamaecyparis obtusa var. formosana

Lychnophora ericoides

1 reference

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Analgesic activity of the lignans from Lychnophora ericoides

Piper philippinum

1 reference

stated in

Lignans, an amide and anti-platelet activities from Piper philippinum

Zanthoxylum ailanthoides

2 references

stated in

Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils

stated in

Isolation of anti-tumor compounds from the stem bark of Zanthoxylum ailanthoides Sieb. & Zucc. by silica gel column and counter-current chromatography

Anthriscus sylvestris

1 reference

stated in

Antiproliferative constituents in umbelliferae plants. IV. Constituents in the fruits of Anthriscus sylvestris Hoffm

Aristolochia chamissonis

2 references

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Rearranged (4→2)-abeo-clerodane and clerodane diterpenes from Aristolochia chamissonis

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Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

Aristolochia cucurbitifolia

1 reference

stated in

The constituents of the root and stem of Aristolochia cucurbitifolia Hayata and their biological activity

Aristolochia elegans

2 references

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The alkaloids and other constituents from the root and stem of Aristolochia elegans

stated in

Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

Aristolochia gehrtii

1 reference

stated in

Alkamides and phenethyl derivatives from Aristolochia gehrtii

Chamaecyparis formosensis

1 reference

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Terpenes and lignans from leaves of Chamaecyparis formosensis

Chamaecyparis obtusa

1 reference

stated in

New lignans from the heartwood of Chamaecyparis obtusa var. formosana

Illicium merrillianum

1 reference

stated in

Brine shrimp lethality test active constituents and new highly oxygenated seco-prezizaane-type sesquiterpenes from Illicium merrillianum

Myristica cinnamomea

1 reference

stated in

Atropisomeric myristinins: selective COX-2 inhibitors and antifungal agents from Myristica cinnamomea

Phyllanthus virgatus

2 references

stated in

A New Lignan fromPhyllanthus virgatus

stated in

Screening of 25 compounds isolated from Phyllanthus species for anti‐human hepatitis B virus in vitro

Piper nigrum

1 reference

stated in

CYP3A4 Inhibitory Activity of New Bisalkaloids, Dipiperamides D and E, and Cognates from White Pepper

Piper trichostachyon

1 reference

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Lignans of Piper trichostachyon

Taiwania cryptomerioides

2 references

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Cytotoxicity of extractives from Taiwania cryptomerioides heartwood

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New Lignans from the Roots ofTaiwania cryptomerioidesHayata

Virola carinata

1 reference

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Neolignans from Virola carinata fruit

Virola michelii

1 reference

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Lignans from kernels of Virola michelii Heckel

Virola multinervia

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Lignoids from the fruit of three Virola species

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Lignans and benzoic acid derivatives from pericarps of Virola multinervia (Myristicaceae)

Zanthoxylum petiolare

2 references

stated in

Isolation of Lignans and Sesquiterpenoids from Leaves ofZanthoxylum Naranjillo

stated in

Isolation of anti-tumor compounds from the stem bark of Zanthoxylum ailanthoides Sieb. & Zucc. by silica gel column and counter-current chromatography

Virola sebifera

1 reference

stated in

Dibenzylbutyrolactone lignans from Virola sebifera

Juniperus sabina

1 reference

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Acetylated lignans from Juniperus sabina

Linum corymbulosum

1 reference

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Diarylbutyrolactone lignans from Linum corymbulosum in vitro cultures

Zanthoxylum dimorphophyllum

1 reference

stated in

Cytotoxic Constituents from the Stem Bark ofZanthoxylum Pistaciiflorum

Aristolochia indica

1 reference

stated in

Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

Phyllanthus urinaria

1 reference

stated in

Screening of 25 compounds isolated from Phyllanthus species for anti‐human hepatitis B virus in vitro

Eleutherococcus divaricatus

1 reference

stated in

Inhibitory lignans against NFAT transcription factor from Acanthopanax koreanum

Aristolochia littoralis

2 references

stated in

The alkaloids and other constituents from the root and stem of Aristolochia elegans

stated in

Antitrypanosomal activity of a diterpene and lignans isolated from Aristolochia cymbifera.

Virola surinamensis

1 reference

stated in

Lignoids, flavanoids and polyketides of Virola surinamensis

Identifiers

InChI

InChI=1S/C20H18O6/c21-20-15(6-13-2-4-17-19(8-13)26-11-24-17)14(9-22-20)5-12-1-3-16-18(7-12)25-10-23-16/h1-4,7-8,14-15H,5-6,9-11H2/t14-,15+/m0/s1

1 reference

language of work or name

Hinokinin (English)

4 October 2016

DDWGQGZPYDSYEL-LSDHHAIUSA-N

2 references

language of work or name

Hinokinin (English)

4 October 2016

ChEBI release 2020-09-01

2 references

language of work or name

hinokinin (English)

4 October 2016

DDWGQGZPYDSYEL-LSDHHAIUSA-N

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=26543-89-5

1 reference

language of work or name

English

title

2(3H)-Furanone, dihydro-3,4-dipiperonyl-, trans-(-)- (English)

4 October 2016

1 reference

language of work or name

English

title

Hinokinin (English)

retrieved

4 October 2016

Reaxys registry number

95369

1 reference

language of work or name

hinokinin (English)

4 October 2016

mapping relation type

1 reference

language of work or name

hinokinin (English)

4 October 2016

1 reference

language of work or name

HINOKININ (English)

4 October 2016

1 reference

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DSSTOX compound identifier

DTXCID401377585

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Human Metabolome Database ID

HMDB0304571

1 reference

based on heuristic

inferred from InChIKey

1 reference

language of work or name

hinokinin (English)

4 October 2016

1 reference

language of work or name

hinokinin (English)

4 October 2016

1 reference

Immune Epitope Database and Analysis Resource

IEDB Epitope ID

116880

retrieved

1 March 2022

Google Knowledge Graph ID

/g/11jfgvlz8f

0 references

Sitelinks

Wikipedia(2 entries)

enwiki Hinokinin
trwiki Hinokinin

(Q27089355)

hinokinin

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Wikipedia(2 entries)

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