Scientific name	Authority	First published in
Sphaeranthus hirtus	Willd.	Sp. Pl., ed. 4 , 3: 2395 (1803)
Oligolepis indicus	Cass. ex Steud.	Nomencl. Bot. 2: 210 (1841)
Sphaeranthus mollis	Roxb.	Hort. Bengal. 62. 1814 [Jun-Dec 1814] ; Fl. Ind. iii. 446
Sphaeranthus mollis	Roxb. ex DC.	Prodromus Systematis Naturalis Regni Vegetabilis 5: 369 1836

Common names Top

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Filter by language:

Language	Common/alternative name
English	east india globe thistle
English	east indian globe thistle
Arabic	زر الورد
Arabic	حبقبق
Arabic	كراوية الأزهار الهندية
Bengali	মুন্ডি
Bengali	মুরমুরিয়া
Hindi	गोरखमुंडी
Kannada	ಮೂಡುಗಟ್ಟಿನ ಗಿಡ
Malayalam	അടയ്ക്കാമണിയൻ
Marathi	गोरखमुंडी
Oriya	ପାଟଫୁଲିଆ
Oriya	ବାଟୁଆଗୋଡ଼ି
Oriya	ମଣ୍ଡାଖିଆ
Oriya	ଭୁଇଁ କଦମ୍ବ
Tamil	கரந்தை மலர்
Tamil	கொண்டைக் கரந்தை
Chinese	麻腊干
Chinese	绒毛戴星草
Chinese	戴星草

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland
  - South Australia
  - Western Australia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000014099
UNII	38527W4B66
Tropicos	2701345
KEW	urn:lsid:ipni.org:names:250536-1
The Plant List	gcc-113632
Open Tree Of Life	852227
NCBI Taxonomy	1205786
IUCN Red List	177190
IPNI	250536-1
iNaturalist	443879
GBIF	3094721
Freebase	/m/0_lhpxx
EPPO	SPSIN
USDA GRIN	401864
Wikipedia	Sphaeranthus_indicus

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

Conductivity-Based Gas Sensors Using Tamarindus indica Polysaccharide-Capped Gold Nanoparticles for the Detection of Volatile Gases

Selvanayakam S, Esakkidurai SP, Kalaiyar S

ACS Omega

24-Feb-2024

PMCID:	PMC10918775
doi:	10.1021/acsomega.3c09137
PMID:	38463309

The Potentials of Ageratum conyzoides and Other Plants from Asteraceae as an Antiplasmodial and Insecticidal for Malaria Vector: An Article Review

Kusman IT, Pradini GW, Ma’ruf IF, Fauziah N, Berbudi A, Achadiyani A, Wiraswati HL

Infect Drug Resist

07-Nov-2023

PMCID:	PMC10638911
doi:	10.2147/IDR.S433328
PMID:	37954507

Editorial: Developing Medicines (Drugs) derived from the Asteraceae—an opportunity in ethnopharmacology, Volume II

da Silva LC, Sahal D, Panda SK

Front Pharmacol

27-Sep-2023

PMCID:	PMC10569686
doi:	10.3389/fphar.2023.1285815
PMID:	37841909

Could Natural Products Help in the Control of Obesity? Current Insights and Future Perspectives

Park J, Nurkolis F, Won H, Yang J, Oh D, Jo H, Choi J, Chung S, Kurniawan R, Kim B

Molecules

13-Sep-2023

PMCID:	PMC10534927
doi:	10.3390/molecules28186604
PMID:	37764380

7-Hydroxy Frullanolide Ameliorates Isoproterenol-Induced Myocardial Injury through Modification of iNOS and Nrf2 Genes

Ullah S, Ahmad T, Ikram M, Rasheed HM, Khan MI, Khan T, Alsahli TG, Alzarea SI, Althobaiti M, Shah AJ

Biomedicines

06-Sep-2023

PMCID:	PMC10526241
doi:	10.3390/biomedicines11092470
PMID:	37760913

IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors

Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP

Int J Biol Sci

06-Aug-2023

PMCID:	PMC10496512
doi:	10.7150/ijbs.85158
PMID:	37705738

Wound healing potential of Vakeri fortified KampillakadiTaila

Dhawal PP, Gharpure M, Joshi MS, Khan RR, Barve SS

J Ayurveda Integr Med

26-May-2023

PMCID:	PMC10236188
doi:	10.1016/j.jaim.2023.100721
PMID:	37245340

General toxicity studies of alpha mangostin from Garcinia mangostana: A systematic review

Setyawati LU, Nurhidayah W, Khairul Ikram NK, Mohd Fuad WE, Muchtaridi M

Heliyon

08-May-2023

PMCID:	PMC10196863
doi:	10.1016/j.heliyon.2023.e16045
PMID:	37215800

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications

Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK

Antibiotics (Basel)

08-Mar-2023

PMCID:	PMC10044610
doi:	10.3390/antibiotics12030543
PMID:	36978410

Biological Activity of Cyclic Peptide Extracted from Sphaeranthus amaranthoides Using De Novo Sequencing Strategy by Mass Spectrometry for Cancer

Yanamadala S, Shanthirappan S, Kannan S, Chiterasu N, Subramanian K, Al-Keridis LA, Upadhyay TK, Alshammari N, Saeed M, Srinivasan GP, Karunakaran R

Biology (Basel)

07-Mar-2023

PMCID:	PMC10045366
doi:	10.3390/biology12030412
PMID:	36979104

Green Synthesis of Iridium Nanoparticles from Winery Waste and Their Catalytic Effectiveness in Water Decontamination

Mergola L, Carbone L, Stomeo T, Del Sole R

Materials (Basel)

02-Mar-2023

PMCID:	PMC10004582
doi:	10.3390/ma16052060
PMID:	36903175

In Vitro and In Vivo Anti-Inflammatory Properties of the Hydroethanolic Extract of the Roots of Vernonia guineensis (Asteraceae)

Yousseu Nana W, Billong Mimb JR, Atsamo AD, Tsafack EG, Djuichou Nguemnang SF, Fagni Njoya ZL, Matah Marthe VM, Madjo Kouam YK, Mbiantcha M, Ateufack G

Int J Inflam

01-Mar-2023

PMCID:	PMC9995193
doi:	10.1155/2023/7915367
PMID:	36909893

A proprietary blend of Sphaeranthus indicus flower head and Mangifera indica bark extracts increases muscle strength and enhances endurance in young male volunteers: a randomized, double-blinded, placebo-controlled trial

Rokkam MP, Gora O, Konda MR, Koushik A

Food Nutr Res

27-Jan-2023

PMCID:	PMC9899043
doi:	10.29219/fnr.v67.8972
PMID:	36794013

Multiple Site Dissimilarities of Herbaceous Species Due to Coal Fly Ash Dumping Based Soil Heavy Metal Toxication

Singh DK, Singh A, Gacem A, Kashyap S, Yadav VK, Yadav KK, Hussein HS, Shukla NK, Alsuhaibani AM, Abdellattif MH, Lee C, Lee W, Modi T, Jeon BH

Toxics

18-Jan-2023

PMCID:	PMC9968134
doi:	10.3390/toxics11020090
PMID:	36850966

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 / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(+)-4-Epi-cryptomeridiol	70698175	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
(1S,4aR,7R,8aR)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-decalin-1-ol	11184061	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol	4655876	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
Proximadiol	165258	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aR,9aR,9bR)-3a,9a-dihydroxy-5a-methyl-3,9-dimethylidene-4,5,6,7,8,9b-hexahydrobenzo[g][1]benzofuran-2-one	15765551	Click to see CC12CCCC(=C)C1(C3C(CC2)(C(=C)C(=O)O3)O)O	264.32	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
(3aR,5aR,9bR)-5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	163002113	Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3	232.32	unknown	https://doi.org/10.1002/CHIN.200725178
(3aR,5aS,9bS)-3a-hydroxy-5a,9-dimethyl-3-methylidene-5,6,7,9b-tetrahydro-4H-benzo[g][1]benzofuran-2,8-dione	15765550	Click to see CC1=C2C3C(CCC2(CCC1=O)C)(C(=C)C(=O)O3)O	262.30	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
(3R,3aR,5aR,8R,9bR)-3a,8-dihydroxy-3,5a,9-trimethyl-3a,4,5,5a,6,7,8,9b-octahydronaphtho[1,2-b]furan-2(3H)-one	138394739	Click to see CC1C(=O)OC2C1(CCC3(C2=C(C(CC3)O)C)C)O	266.33	unknown	https://doi.org/10.1002/CHIN.200725178
(3R,3aR,5aR,9bS)-3a-hydroxy-3,5a,9-trimethyl-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	101673189	Click to see CC1C(=O)OC2C1(CCC3(C2=C(CCC3)C)C)O	250.33	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
(3R,3aR,5aS,7S,9bS)-3a,7-dihydroxy-3,5a,9-trimethyl-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	14589100	Click to see CC1C(=O)OC2C1(CCC3(C2=C(CC(C3)O)C)C)O	266.33	unknown	https://doi.org/10.1002/CHIN.200419179
(3S,3aR,5aR,8S,9bS)-3a-hydroxy-3,5a,9-trimethyl-8-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	154497491	Click to see CC1C(=O)OC2C1(CCC3(C2=C(C(CC3)OC4C(C(C(C(O4)CO)O)O)O)C)C)O	428.50	unknown	https://doi.org/10.1016/0031-9422(90)85191-H
3a-hydroxy-3,5a,9-trimethyl-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	13995530	Click to see CC1C(=O)OC2C1(CCC3(C2=C(CCC3)C)C)O	250.33	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
3a-hydroxy-3,5a,9-trimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	14733721	Click to see CC1C(=O)OC2C1(CCC3(C2=C(C(CC3)OC4C(C(C(C(O4)CO)O)O)O)C)C)O	428.50	unknown	https://doi.org/10.1016/0031-9422(90)85191-H
3a-hydroxy-5a,9-dimethyl-3-methylidene-5,6,7,9b-tetrahydro-4H-benzo[g][1]benzofuran-2,8-dione	77175428	Click to see CC1=C2C3C(CCC2(CCC1=O)C)(C(=C)C(=O)O3)O	262.30	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
3a,7-dihydroxy-3,5a,9-trimethyl-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	14589099	Click to see CC1C(=O)OC2C1(CCC3(C2=C(CC(C3)O)C)C)O	266.33	unknown	https://doi.org/10.1002/CHIN.200419179
3a,8-dihydroxy-3,5a,9-trimethyl-4,5,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2-one	14312974	Click to see CC1C(=O)OC2C1(CCC3(C2=C(C(CC3)O)C)C)O	266.33	unknown	https://doi.org/10.1002/CHIN.200725178
3a,9a-Dihydroxy-5a-methyl-3,9-dimethylidene-4,5,6,7,8,9b-hexahydrobenzo[g][1]benzofuran-2-one	85447409	Click to see CC12CCCC(=C)C1(C3C(CC2)(C(=C)C(=O)O3)O)O	264.32	unknown	https://doi.org/10.1016/0031-9422(92)83492-H
5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	3478505	Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3	232.32	unknown	https://doi.org/10.1002/CHIN.200725178
Sphaeranthanolide	14733722	Click to see CC1C(=O)OC2C1(CCC3(C2=C(C(CC3)OC4C(C(C(C(O4)CO)O)O)O)C)C)O	428.50	unknown	https://doi.org/10.1016/0031-9422(90)85191-H
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5-hydroxy-7-methoxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	162886299	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)C4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149149/
5-Hydroxy-7-methoxy-2-phenyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	162886298	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)C4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149149/
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-5-methoxy-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163103903	Click to see CC(=CCC1=C(C(=CC(=C1)C2=COC3=C(C2=O)C(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)C	544.50	unknown	https://doi.org/10.1016/S0367-326X(98)00018-5

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Sphaeranthus indicus

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top