Teucrium japonicum in Genus Teucrium

Database	ID/link to page
World Flora Online	wfo-0000322222
Tropicos	50004803
KEW	urn:lsid:ipni.org:names:460483-1
The Plant List	kew-203010
Open Tree Of Life	5232638
Observations.org	129716
NCBI Taxonomy	1209863
IPNI	460483-1
iNaturalist	924892
GBIF	3896071
EPPO	TEUJA
EOL	2894341
Elurikkus	435718

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Lamiaceae: An Insight on Their Anti-Allergic Potential and Its Mechanisms of Action

Sim LY, Abd Rani NZ, Husain K

Front Pharmacol

19-Jun-2019

PMCID:	PMC6594199
doi:	10.3389/fphar.2019.00677
PMID:	31275149

Screening of promising chemotherapeutic candidates from plants extracts

Kinjo J, Nakano D, Fujioka T, Okabe H

J Nat Med

16-Apr-2016

PMCID:	PMC4935755
doi:	10.1007/s11418-016-0992-2
PMID:	27086008

Studies on the furanoid diterpenes from Teucrium japonicum Houtt.

TOSHIO MIYASE, HIROKO KAWASAKI, TADATAKA NORO, AKIRA UENO, SEIGO FUKUSHIMA, TSUNEMATSU TAKEMOTO

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.29.3561

A neo-clerodane diterpene from Teucrium japonicum

Min Zhi-Daz, Xie Ning, Zhang Pei, Zhao Shou-Zun, Wang Chong-Sh, Zheng Qi-Tai

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(91)83494-6

C-12 stereochemistry of teupolin I and related diterpenoids from Teucrium species

Georgi Y. Papanov, Peter Y. Malakov, László Szilágyi, Eszter Gács-Baitz

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)81772-0

Neo-clerodane diterpenoids from Teucrium pernyi

Xie Ning, Min Zhi-da, Zhao Shou-xun, Wu Bing, Zheng Qi-tai, Zhang Pei

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(91)85048-5

Teucrol, a decarboxyrosmarinic acid and its 4'-O-triglycoside, teucroside from Teucrium pilosum.

El-Mousallamy AM, Hawas UW, Hussein SA

Phytochemistry

01-Dec-2000

doi:	10.1016/S0031-9422(00)00218-1
PMID:	11140526

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(1R,5'S,8S,9R,10R)-5'-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4(12)-ene-9,3'-oxolane]-2',3-dione	163195110	Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=CC(OC5=O)O)C(=O)O2	360.40	unknown	https://doi.org/10.1016/0031-9422(91)85048-5
5'-(2-hydroxy-5-oxo-2H-furan-4-yl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4(12)-ene-9,3'-oxolane]-2',3-dione	162977809	Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=CC(OC5=O)O)C(=O)O2	360.40	unknown	https://doi.org/10.1016/0031-9422(91)83494-6 https://doi.org/10.1016/0031-9422(91)85048-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
2-[4-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxyphenyl]ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	162882926	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(OC(C(C3O)O)OC4=C(C=C(C=C4)CCOC(=O)C=CC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O)O	770.70	unknown	https://doi.org/10.1016/S0031-9422(00)00218-1
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 13855360	13855360	Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O	404.50	unknown	https://doi.org/10.1248/CPB.29.3561
CID 3036768	3036768	Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O	404.50	unknown	https://doi.org/10.1248/CPB.29.3561
Eugarzasidine I	316446	Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2	328.40	unknown	https://doi.org/10.1248/CPB.29.3561
Teucvin	179592	Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2	328.40	unknown	https://doi.org/10.1248/CPB.29.3561
Teupolin I	156030	Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O	404.50	unknown	https://doi.org/10.1248/CPB.29.3561 https://doi.org/10.1016/S0031-9422(00)81772-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3-(3,4-Dihydroxy-phenyl)-acrylic acid 2-(3,4-dihydroxy-phenyl)-ethyl ester	20979949	Click to see C1=CC(=C(C=C1CCOC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	316.30	unknown	https://doi.org/10.1016/S0031-9422(00)00218-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/0031-9422(91)85048-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	284.26	unknown	https://doi.org/10.1016/0031-9422(91)83494-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	https://doi.org/10.1016/0031-9422(91)85048-5 https://doi.org/10.1016/0031-9422(91)83494-6

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Teucrium japonicum

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