Scientific name	Authority	First published in
Dianthus altaicus	Willd. ex Ledeb.	Fl. Ross. 1: 278. 1842.
Dianthus chinensis f. albiflora	Y.N.Lee	in Bull. Korea Pl. Res. 4: 28. 2004.
Dianthus chinensis var. ignescens	Nakai	in Rep. Exped. Manchoukou Sect. IV 4(2): 15. 1935.
Dianthus chinensis var. jingpoensis	G.Y.Zhang & X.Y.Yuan	in Bull. Bot. Res., Harbin 18: 10. 1998.
Dianthus chinensis var. liaotungensis	Y.C.Chu	Fl. Plant. Herb. Chinae bor.-or. 3: 227. 1975.
Dianthus chinensis var. longisquama	Nakai & Kitag.	in Rep. Exped. Manchoukou Sect. IV 1: 23. 1934.
Dianthus chinensis var. macrosepalus	Franch. ex L.H.Bailey	Cycl. Amer. Hort.: 100. 1900.
Dianthus chinensis var. morii	(Nakai) Y.C.Chu	Fl. Plant. Herb. Chinae bor.-or. 3: 49. 1975.
Dianthus chinensis subsp. paracampestris	Vorosch.	in Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. n.s., 83(5): 116. 1978.
Dianthus chinensis var. serpens	Y.N.Lee	in Bull. Korea Pl. Res. 4: 29. 2004.
Dianthus chinensis var. shandongensis	J.X.Li & F.Q.Zhou	in Bull. Bot. Res., Harbin 21: 511. 2001.
Dianthus chinensis var. subulifolius	(Kitag.) Y.C.Ma	Fl. Intramongolica 2: 191. 1978.
Dianthus chinensis var. sylvaticus	W.D.J.Koch	Syn. Fl. Germ. Helv.: 96. 1835.
Dianthus chinensis var. trinervis	D.Q.Lu	in Bull. Bot. Res., Harbin 15: 185. 1995.
Dianthus chinensis var. versicolor	(Fisch. ex Link) Y.C.Ma	Fl. Intramongolica 2: 191. 1978.
Dianthus chinensis subsp. versicolor	(Fisch. ex Link) Vorosch.	Florist. Issl. Razn. Rayonakh SSSR: 167. 1985.
Dianthus dentosus	Fisch. ex Rchb.	in Iconogr. Bot. Pl. Crit. 6: 32. 1828.
Dianthus fischeri	Spreng.	Pl. Min. Cogn. Pug. 2: 62. 1815.
Dianthus ibericus	Willd.	Enum. Pl., Suppl.: 24. 1814.
Dianthus jeniseensis	Less. ex Ledeb.	Fl. Ross. 1: 278. 1842.
Dianthus laciniatus	Makino	in Bot. Mag. (Tokyo) 17: 60. 1903.
Dianthus morii	Nakai	in Bot. Mag. (Tokyo) 28: 302. 1914.
Dianthus ochroleucus	Link	Enum. Hort. Berol. Alt. 1: 420. 1821.
Dianthus patens	Willd.	Enum. Pl., Suppl.: 24. 1814.
Dianthus pineticola	Kleopow	in Izv. Kievsk. Bot. Sada 12-13: 161. 1931.
Dianthus pulcher	Salisb.	Prodr. Stirp. Chap. Allerton: 303. 1796.
Dianthus ruthenicus	Roem. ex Poir.	Encycl. Suppl. 4: 131. 1816.
Dianthus scaber	Schleich. ex Suter	Fl. Helv. i. 259.
Dianthus schraderi	Rchb.	in Iconogr. Bot. Exot. 1: 24. 1824.
Dianthus sinensis	Link	Handbuch 2: 237. 1831.
Dianthus subulifolius	Kitag.	in Rep. Exped. Manchoukou Sect. IV 2: 16. 1935.
Dianthus tataricus	Fisch.	Cat. Jard. Gorenki ed. 2: 59. 1812.
Dianthus umbellatus	DC.	Cat. Pl. Horti Monsp.: 104. 1813.
Dianthus versicolor	Fisch. ex Link	Enum. Hort. Berol. Alt. 1: 420. 1821.
Dianthus versicolor f. leucopetalus	(Kitag.) Y.C.Chu	Fl. Plant. Herb. Chinae bor.-or. 3: 50. 1975.
Dianthus versicolor var. ninelli	Peschkova	Fl. Tsentralnoi Sibiri 1: 334. 1979.
Dianthus versicolor var. subulifolius	(Kitag.) Y.C.Chu	Fl. Plant. Herb. Chinae bor.-or. 3: 50. 1975.
Dianthus willdenowii	Link	Enum. Hort. Berol. Alt. 1: 420. 1821.
Dianthus chinensis f. ignescens	(Nakai) Kitag.	in J. Jap. Bot. 34: 5. 1959.
Dianthus chinensis var. dentosus	(Fisch. ex Rchb.) Debeaux	in Act. Simpo. Internac. Bot. Pius Font Quer 31: 124. 1876.
Dianthus seguieri var. dentosus	(Fisch. ex Rchb.) Franch.	Pl. David. 1: 46. 1884.
Dianthus subulifolius f. leucopetalus	Kitag.	in Rep. Exped. Manchoukou Sect. IV 2: 17. 1935.
Dianthus sequieri	Chaix	Vill. Fl. Dauph. 1: 330. 1786.
Dianthus sequieri var. dentosus	(Fisch. ex Rchb.) Franch.	Pl. David. 1: 46. 1884.
Dianthus versicolor var. alpinus	Krylov	Fl. Zapadnoi Sibiri 5: 1104. 1931.
Dianthus versicolor subsp. ninelli	(Peschkova) Baikov & N.V.Vlassova	Rast. Mir Aziatsk. Rossii 3(23): 21. 2016.
Dianthus collinus var. scaber	(Schleich. ex Suter) Gaudin	Fl. Helv. 3: 147. 1828.
Dianthus serratus var. scaber	(Schleich. ex Suter) DC.	Fl. Franç. 5: 601. 1815.

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese pink
English	rainbow pink
English	chinese pink
English	china pink
English	annual pink
English	indian pink
Arabic	قرنفل صيني
Azerbaijani	Çin qərənfili
Bulgarian	китайски карамфил
Catalan	clavell del japó
Catalan	clavell de la xina
Czech	hvozdík čínský
German	heddewigsnelke
German	chinesernelke
German	chineser-nelke
German	kaisernelke
German	chinesische nelke
Estonian	hiina nelk
Basque	txinatar krabelin
Finnish	kiinanneilikka
French	Œillet de chine
Upper Sorbian	chinska nalika
Armenian	Մեխակ չինական
Indonesian	anyelir cina
Japanese	カラナデシコ
Japanese	石竹
Japanese	セキチク
Korean	패랭이꽃
Lithuanian	kininis gvazdikas
Latvian	fišera neļķe
lzh	石竹
Norwegian Bokmål	kinesernellik
Dutch	chinese anjer
Polish	goździk chiński
Russian	Гвоздика китайская
Swedish	sommarnejlika
Turkish	Çin karanfili
Ukrainian	гвоздики китайські
Chinese	石竹花
Chinese	洛陽花
Chinese	剪絨花
Chinese	蒙古石竹
Chinese	石竹，洛阳花
Chinese	瞿麦
Chinese	山猫儿
Chinese	石竹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Xinjiang
- Eastern Asia
  - Korea
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Magadan
  - Primorye
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - West Himalaya
- Indo-China
  - Vietnam

Europe click to expand
- Eastern Europe
  - Central European Russia
  - East European Russia
  - Krym
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Czechoslovakia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000643302
UNII	E097DJ9EN0
Canadensys	4286
USDA Plants	DICH3
Tropicos	6301210
INPN	445555
KEW	urn:lsid:ipni.org:names:153215-1
The Plant List	kew-2764027
Missouri Botanical Garden	279090
Open Tree Of Life	231868
NCBI Taxonomy	118431
NBN Atlas	NBNSYS0000014173
Nature Serve	2.140987
IPNI	153215-1
iNaturalist	161763
GBIF	3085418
Freebase	/m/067t7b
EPPO	DINCH
EOL	486532
Elurikkus	4303
USDA GRIN	13827
Wikipedia	Dianthus_chinensis

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

Progress of medicinal plants and their active metabolites in ischemia-reperfusion injury of stroke: a novel therapeutic strategy based on regulation of crosstalk between mitophagy and ferroptosis

Zhang G, Wang Q, Jiang B, Yao L, Wu W, Zhang X, Wan D, Gu Y

Front Pharmacol

08-Apr-2024

PMCID:	PMC11033413
doi:	10.3389/fphar.2024.1374445
PMID:	38650626

Phytochemical, Nutritional and Mineral Content of Four Edible Flowers

Marchioni I, Gabriele M, Carmassi G, Ruffoni B, Pistelli L, Pistelli L, Najar B

Foods

20-Mar-2024

PMCID:	PMC10969817
doi:	10.3390/foods13060939
PMID:	38540929

Zinc and sulfur functionalized biochar as a peroxydisulfate activator via deferred ultraviolet irradiation for tetracycline removal

Qin Y, Wang S, Zhang B, Chen W, An M, Yang Z, Gao H, Qin S

RSC Adv

13-Feb-2024

PMCID:	PMC10863648
doi:	10.1039/d3ra07923f
PMID:	38352677

Research progress of Paris polyphylla in the treatment of digestive tract cancers

Wang J, Ni BY, Wang J, Han L, Ni X, Wang XM, Cao LC, Sun QH, Han XP, Cui HJ

Discov Oncol

07-Feb-2024

PMCID:	PMC10850040
doi:	10.1007/s12672-024-00882-9
PMID:	38324023

Ecophysiology of Antarctic Vascular Plants: An Update on the Extreme Environment Resistance Mechanisms and Their Importance in Facing Climate Change

Ramírez CF, Cavieres LA, Sanhueza C, Vallejos V, Gómez-Espinoza O, Bravo LA, Sáez PL

Plants (Basel)

03-Feb-2024

PMCID:	PMC10857404
doi:	10.3390/plants13030449
PMID:	38337983

Effect of traditional Chinese medicine in osteosarcoma: Cross-interference of signaling pathways and potential therapeutic targets

Liu Y, Jiang B, Li Y, Zhang X, Wang L, Yao Y, Zhu B, Shi H, Chai X, Hu X, Zhang B, Li H

Medicine (Baltimore)

19-Jan-2024

PMCID:	PMC10798715
doi:	10.1097/MD.0000000000036467
PMID:	38241548

Impact of Preparative Isolation of C-Glycosylflavones Derived from Dianthus superbus on In Vitro Glucose Metabolism

Lin Z, Zhou X, Yuan C, Fang Y, Zhou H, Wang Z, Dang J, Li G

Molecules

09-Jan-2024

PMCID:	PMC10820209
doi:	10.3390/molecules29020339
PMID:	38257252

Embryological observations on seed abortion in Hibiscus syriacus L. and physiological studies on nutrients, enzyme activity and endogenous hormones

Wang X, Chen J, Hu L, Zhang J, Xiao F, Zhang S, Shao F, Huang L

BMC Plant Biol

21-Dec-2023

PMCID:	PMC10740302
doi:	10.1186/s12870-023-04669-y
PMID:	38129795

The Impact and Determinants of Mountainous Topographical Factors on Soil Microbial Community Characteristics

Yu J, Li S, Sun X, Zhou W, He L, Zhao G, Chen Z, Bai X, Zhang J

Microorganisms

28-Nov-2023

PMCID:	PMC10746091
doi:	10.3390/microorganisms11122878
PMID:	38138022

The effects of precipitation change on urban meadows in different design models and substrates

Jiang Y, Yuan T

Sci Rep

23-Nov-2023

PMCID:	PMC10667351
doi:	10.1038/s41598-023-44974-y
PMID:	37996501

Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses

Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ

Foods

08-Nov-2023

PMCID:	PMC10671036
doi:	10.3390/foods12224066
PMID:	38002124

Complete chloroplast genomes of Cerastium alpinum, C. arcticum and C. nigrescens: genome structures, comparative and phylogenetic analysis

Milarska SE, Androsiuk P, Paukszto Ł, Jastrzębski JP, Maździarz M, Larson KW, Giełwanowska I

Sci Rep

31-Oct-2023

PMCID:	PMC10618263
doi:	10.1038/s41598-023-46017-y
PMID:	37907682

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Secondary succession of shrub-herb communities in the hilly area of Taihang Mountain

Liu X, Zhou W, Li X, Zhang Y, Dong W

Front Plant Sci

08-Sep-2023

PMCID:	PMC10514918
doi:	10.3389/fpls.2023.1194083
PMID:	37746017

Four New Species of Small-Spored Alternaria Isolated from Solanum tuberosum and S. lycopersicum in China

Gou Y, Aung SL, Guo Z, Li Z, Shen S, Deng J

J Fungi (Basel)

27-Aug-2023

PMCID:	PMC10532295
doi:	10.3390/jof9090880
PMID:	37754988

Phytochemical Profile Top

Add a new one!

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,4S,4aR,6aR,6bS,8R,8aR,12aS,14aR,14bR)-3,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	102272774	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	664.80	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
(3S,4S,4aR,6aR,6bS,8R,8aR,12aS,14aR,14bR)-3,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	162896131	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)O)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C	827.00	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
(3S,4S,4aR,6aR,6bS,8R,8aR,12aS,14aR,14bR)-8-hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	101786835	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)OC6C(C(C(CO6)O)O)O)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C	959.10	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
3,8-Dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	74413301	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	664.80	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
3,8-Dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	162896130	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)O)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C	827.00	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
8-Hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-(3,4,5-trihydroxyoxan-2-yl)oxy-8a-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	162962255	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)OC6C(C(C(CO6)O)O)O)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C	959.10	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
8a-O-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 4-O-[(2R)-2-hydroxypropyl] (3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	162899407	Click to see CC(COC(=O)C1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)O	1031.20	unknown	https://doi.org/10.1016/S0040-4020(01)81202-3
8a-O-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 4-O-[(2S)-2-hydroxypropyl] (3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	162899408	Click to see CC(COC(=O)C1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)O	1031.20	unknown	https://doi.org/10.1016/S0040-4020(01)81202-3
8a-O-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] 4-O-[(2R)-2-hydroxypropyl] (3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	162963605	Click to see CC(COC(=O)C1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)O	1193.30	unknown	https://doi.org/10.1016/S0040-4020(01)81202-3
8a-O-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] 4-O-[(2S)-2-hydroxypropyl] (3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	163192069	Click to see CC(COC(=O)C1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)O	1193.30	unknown	https://doi.org/10.1016/S0040-4020(01)81202-3
8a-O-[3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 4-O-(2-hydroxypropyl) 3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	162899406	Click to see CC(COC(=O)C1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)O	1031.20	unknown	https://doi.org/10.1016/S0040-4020(01)81202-3
8a-O-[6-[[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] 4-O-(2-hydroxypropyl) 3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	162963604	Click to see CC(COC(=O)C1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)O	1193.30	unknown	https://doi.org/10.1016/S0040-4020(01)81202-3
bis[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4S,4aR,6aR,6bS,8R,8aR,12aS,14aR,14bR)-3,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	163047903	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	827.00	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
Bis[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	163047902	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	827.00	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
Dianchinenoside B	133562223	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C(=O)O)OC6C(C(C(CO6)O)O)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	796.90	unknown	https://doi.org/10.1021/NP50097A009
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
2,6-Dideoxy-3-O-ethyl-alpha-L-arabino-Hexopyranose	131067433	Click to see CCOC1CC(OC(C1O)C)O	176.21	unknown	https://doi.org/10.1016/0008-6215(94)90026-4
4-Ethoxy-6-methyloxane-2,5-diol	133627136	Click to see CCOC1CC(OC(C1O)C)O	176.21	unknown	https://doi.org/10.1016/0008-6215(94)90026-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Thermopsoside	11294177	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(00)90599-5

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Dianthus chinensis

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