(Q77462786)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

review article

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title

Pharmacology and chemotaxonomy of Diospyros (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

main subject

Diospyros canaliculata

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Diospyros elliptifolia

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Diospyros diepenhorstii

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Diospyros ehretioides

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Diospyros bipindensis

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Diospyros rotundifolia

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Diospyros candolleana

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Diospyros chaetocarpa

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Diospyros alboflavescens

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Diospyros cinnabarina

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Diospyros mcphersonii

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Diospyros austroafricana

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Diospyros sanza-minika

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Diospyros loureiroana

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Diospyros chloroxylon

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Diospyros monbuttensis

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Diospyros kamerunensis

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Diospyros inhacaensis

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Diospyros gracilescens

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Diospyros obliquifolia

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Diospyros singaporensis

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Diospyros siderophylla

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Diospyros mespiliformis

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Diospyros embryopteris

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(1aS,7aR)-3-hydroxy-4-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-5-methyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione

Diospyros oppositifolia

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Diospyros rheophytica

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Diospyros crassiflora

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Diospyros heterotricha

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(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

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5-Hydroxy-6-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-methoxy-7-methylnaphthalene-1,4-dione

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5-Hydroxy-2,3-bis(2-hydroxy-5-methyl-4-oxochromen-3-yl)-7-methylnaphthalene-1,4-dione

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1',4-Dihydroxy-7'-methoxy-2,3'-dimethyl-,(-)-[1,2'-binaphthalene]-5,5',8,8'-tetrone

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(4R)-4,8-dihydroxy-6-methyl-tetralin-1-one

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2-[(5R)-1,5-dihydroxy-3-methyl-8-oxo-6,7-dihydro-5H-naphthalen-2-yl]-5-hydroxy-7-methylnaphthalene-1,4-dione

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8-Hydroxy-7-(4-hydroxy-6-methoxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-methoxy-6-methylnaphthalene-1,4-dione

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8-hydroxy-2-methoxy-6-methylnaphthalene-1,4-dione

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(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde

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8-Hydroxy-5-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione

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(2,2'-Binaphthalene)-5,5',8,8'-tetrone, 1,1'-dihydroxy-6,6'-dimethyl-

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2-(4,6-Dihydroxy-5-methoxy-2-methylnaphthalen-1-yl)-5-hydroxy-7-methylnaphthalene-1,4-dione

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2-(1,5-Dihydroxy-4-methoxy-7-methylnaphthalen-2-yl)-5-hydroxy-7-methylnaphthalene-1,4-dione

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[2,2'-Binaphthalene]-1,1',4,4'-tetrone, 5,5'-dihydroxy-7,7'-dimethyl-

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(1aS,7aR)-3-hydroxy-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione

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4,5',8'-trihydroxy-6-methoxy-2,3'-dimethyl-[1,2'-binaphthalene]-1',4',5,8-tetrone

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D-Friedoolean-14-en-3-one

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5-Hydroxy-2-(1-hydroxy-3-methyl-5,8-dioxo-6,7-dihydronaphthalen-2-yl)-7-methylnaphthalene-1,4-dione

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Oleanolic acid 3-acetate

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(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

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5-hydroxy-2-methoxy-7-methylnaphthalene-1,4-dione

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5,8'-Dihydroxy-7,6'-dimethyl-2,2'-binaphthalene-1,1',4,4'-tetraone

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5-Hydroxy-7-methyl-tetralin-1,4-dione

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(1R,4R,5R,8R,10S,13S,14R,17R,18R,19R)-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol

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(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol

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8-Hydroxy-7-(4-hydroxy-7-methoxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-methoxy-6-methylnaphthalene-1,4-dione

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5-Hydroxy-2-[5-hydroxy-6-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-7-methyl-1,4-dioxonaphthalen-2-yl]-6-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-7-methylnaphthalene-1,4-dione

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(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one

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1,4-Naphthalenedione, 8-hydroxy-2-methoxy-

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(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol

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8-Hydroxy-2-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione

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(1R,3aR,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol

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Urs-12-ene-3,28-diol, (3beta)-

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17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

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(+)-6',7'-Dihydro-1',5,5'-trihydroxy-3',7-dimethyl-2,2'-binaphthalene-1,4,8'(5'H)-trione

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10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

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5-Hydroxy-2-(5-hydroxy-4-methoxy-7-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-7-methylnaphthalen-1-one

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4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one

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8-Hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one

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4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol

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U V Mallavadhani

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

A K Panda

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

Y R Rao

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

publication date

October 1998

3 references

16 September 2022

16 September 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

49

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

issue

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

page(s)

901-951

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

Termiticidal components of wood extracts: 7-methyljuglone from Diospyros virginiana

5 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinones of Diospyros usambarensis; their Molluscicidal and Fungicidal Activities1

1 reference

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7 January 2021

Extractives from Ebenaceae: Constituents of the Root and Stem Barks of Diospyros verrucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Cytotoxic naphthoquinones, molluscicidal saponins and flavonols from Diospyros zombensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Bush medicine in the Exumas and long island, bahamas a field study

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Studies on the Constituents of the Useful Plants. IV. The Constituents of Calyx of Diospyros kaki. (1)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

The effect of maklua (Diospyros mollis) in the treatment of human hookworm

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Cytotoxic components of Diospyros morrisiana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Pharmacographia indica :A history of the principal drugs of vegetable origin, met with in British India

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Prolongation of life span of stroke-prone spontaneously hypertensive rats (SHRSP) ingesting persimmon tannin.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Hypotensive principles of Diospyros kaki leaves

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Investigations on the Steroidal Anti-Inflammatory Activity of Triterpenoids fromDiospyros leucomelas*

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Antibacterial activity of diosquinone and plumbagin from the root ofDiospyros mespiliformis (Hostch) (Ebenaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Carcinogenicity of Camellia sinensis (Tea) and Some Tannin-Containing Folk Medicinal Herbs Administered Subcutaneously in Rats23

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Anti-inflammatory constituents of topically applied crude drugs. I. Constituents and anti-inflammatory effect of Eriobotrya japonica LINDL

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Anti-HIV triterpene acids from Geum japonicum

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Search for possible antitumor promoters by inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced Epstein-Barr virus activation; ursolic acid and oleanolic acid from an anti-inflammatory Chinese medicinal plant, Glechoma hederaceae L.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Anthracenic Derivatives fromPsorospermum febrifugumand theirin vitroCytotoxicities to a Human Colon Carcinoma Cell Line1

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Biological activity of diospyrin towards Ehrlich ascites carcinoma in Swiss A mice

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Inhibitory effects of various flavonoids isolated from leaves of persimmon on angiotensin-converting enzyme activity

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Studies on carotenoids: The carotenoids of Diospyros fruits. II. The carotenoids of arbutus fruits (Arbutus unedo)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinones from Diospyros hebecarpa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinones and triterpenes from african Diospyros species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinones and triterpenes from some asian Diospyros species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Chemical constituents of Diospyros buxifolia, D. tomentosa, D. ferra, D. lotus, Rhus parviflora, Polygonum recumbens, Balanites aegyptiaca and Pyrus pashia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

3′-methoxydiospyrin, a 7-methyljuglone dimer from diospyros mannii

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Ebenaceae extractives. Part IV. Diosindigo A, a blue pigment from several Diospyros species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

792. Ebenaceae extractives. Part II. Naphthaldehydes from Diospyros ebenum koen

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Constituents of diospyros peregrina fruit and seed

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Peregrinol, a lupane type triterpene from the fruits of Diospyros peregrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Sterols and triterpenes of Diospyros montana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

New naphthoquinones from Diospyros

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

- a novel binaphthaquinone showing atropisomerism and Other extractives from diospyros chloroxylon

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A new brominated naphthoquinone from Diospyros maritima Blume.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinones of Euclea and Diospyros species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinones from the Root and Stem Barks of Diospyros usambarensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Ebenaceae extractives. Part 9. New naphthoquinones and binaphthylquinones from macassar ebony

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Ein neues Naphthochinon aus dem Kernholz vonDiospyros melanoxylon Roxb.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Identification of methylnaphthazarin in Diospyros species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A new class of natural product: homologues of juglone bearing 4-hydroxy-5-methyl-coumarin-3-yl units from Diospyros species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Structure of ebenone, a possible biogenetic precursor of elliptinone, from Diospyros ebenum

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A naphthoquinone carboxylate from fungal infested Diospyros montana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A pentacyclic quinone diosindigo B from the heartwood of Diospyros melanoxylon

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A new binaphthoquinone from Diospyros maritima BLUME.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Xylospyrin - a novel trinaphthylenequinone from diospyros chloroxylon and comments on PMR spectrum of (−) isodiospyrin leucohexaacetate

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Tetrahydrodiospyrin: a reduced binaphthoquinone from the bark of Diospyros montana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

The isoprene rule and the biogenesis of terpenic compounds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Zur Kenntnis der Triterpene. 190. Mitteilung. Eine stereochemische Interpretation der biogenetischen Isoprenregel bei den Triterpenen

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Biosynthesis of dihydromenaquinone-9 by Mycobacterium phlei

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Ebenaceae extractives. Part 10. Macassaric acid, an o-methoxycarbonylcinnamic acid from macassar ebony

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoic acid derivatives from Diospyros ebenum

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

The structure of diospyrol, the principle from the fruit of Diospyros mollis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A new diospyrol glycoside from Diospyros mollis Griff.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Structure d'un nouvel heteroside coumarioue : Le diospyroside

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

4-Hydroxy-5-methylcoumarin fromDiospyros ismailii

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Volatile Compounds from the Fruit Peelings ofDiospyros discolorWilld

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

A New anthraquinone Glycoside from the Stem Bark of Diospyros discolor

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Lignan from calyces of Diospyros kaki

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2901020-0

7 January 2021

Naphthoquinone Derivatives from the Ebenaceae. IV. Naphthoquinone Derivatives from Diospyros kaki THUNB. and D. kaki THUNB. var. sylvestris MAKINO

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.20.2029

Naphthoquinone Derivatives from the Ebenaceae. II. Isodiospyrin, Bisisodiospyrin, and Mamegakinone from Diospyros lotus L. and D. morrisiana HANCE

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.19.2308

Naphthoquinone Derivatives from the Ebenaceae. I. Diospyrol and the Related Naphthoquinones from Diospyros mollis GRIFF.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.19.2271

Identifiers

DOI

10.1016/S0031-9422(97)01020-0

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9788142%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference