Acalypha hispida, also known as the chenille plant, is a flowering shrub native to tropical Asia. It belongs to the family Euphorbiaceae and is the fourth largest genus in the family. It is also known as Philippine medusa and red hot cat tail due to its attractive and brightly colored, furry flowers. The plant can grow up to 12 feet tall and is often cultivated as a houseplant. It is dioecious, meaning there are distinct male and female plants, and the female plants produce clusters of purple to bright red flowers that resemble cat tails. Acalypha hispida is widely cultivated and has gained the Royal Horticultural Society's Award of Garden Merit. It is propagated from cuttings and requires bright light, high humidity, and well-watered soil. The plant is also used for medicinal purposes, but its clear latex is poisonous and can irritate the skin and mucous membranes.

Synonyms Top

Scientific name	Authority	First published in
Acalypha sanderi	N.E.Br.	Gard. Chron. III, 1896: 392 1896
Acalypha sanderi	K.Schum.	Notizbl. Bot. Gart. Berlin-Dahlem 2: 127 1898
Ricinocarpus hispidus	(Burm.f.) Kuntze	Revis. Gen. Pl. 2: 618. 1891 (1891)
Acalypha densiflora	Blume	Bijdr. Fl. Ned. Ind. : 628 (1826)
Acalypha hispida var. sanderi	(N.E.Br.) J.J.Sm.	Meded. Dept. Landb. Ned.-Indië 10: 19. 1910

Common names Top

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Language	Common/alternative name
English	chenille plant
English	red-hot cat's tail
Spanish	manto de candela
Arabic	أكاليفا هيسبيدا
Bengali	শিবঝুল
German	katzenschwänzchen
dv	ބުޅާނިގޫ
Estonian	harjaseline nõgesleht
Persian	آکالیفا هیسپیدا
Finnish	isokissanhäntä
French	queue de minite
French	queue de chat
Upper Sorbian	koča wopuš
Upper Sorbian	Šćeka akalyfa
ht	kechat
Hungarian	érdes kutyacsalán
Indonesian	tanaman ekor kucing
Japanese	ベニヒモノキ
jv	buntut kucing
Lithuanian	akalifa
Lithuanian	Šeriuotoji labravenė
Malayalam	പൂച്ചവാലൻ ചെടി
Malay	pokok ekor kucing
Malay	ekor kucing
pam	iking pusa
Polish	pokrzywiec szorstkowłosy
Polish	pokrzywiec szorstki
Swedish	kattsvans
Vietnamese	tai tượng đuôi chồn
Chinese	铁苋
Chinese	紅花鐵莧
Chinese	狗尾红
Chinese	一种维管植物
Chinese	红穗铁苋菜

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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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Area

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Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Tanzania
- West Tropical Africa
  - Benin
  - Gambia
- West-central Tropical Africa
  - Burundi
  - Equatorial Guinea
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros
  - Madagascar

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
- Indo-China
  - Andaman Islands
  - Nicobar Nicobar
  - Thailand
- Papuasia
  - Bismarck Archipelago

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
  - Marshall Islands
- South-central Pacific
  - Cook Islands
  - Marquesas
  - Society Islands
  - Tuamotu
  - Tubuai Islands
- Southwestern Pacific
  - Gilbert Islands
  - Vanuatu

Southern America click to expand
- Caribbean
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Venezuelan Antilles
- Western South America
  - Ecuador

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000950668
USDA Plants	ACHI2
Tropicos	12800112
INPN	445614
KEW	urn:lsid:ipni.org:names:337478-1
The Plant List	kew-689
Missouri Botanical Garden	280097
Open Tree Of Life	1015290
NCBI Taxonomy	197604
IPNI	337478-1
iNaturalist	208742
GBIF	3056375
Freebase	/m/026ckpn
EPPO	ACCHI
EOL	1145525
USDA GRIN	316293
Wikipedia	Acalypha_hispida

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_948193465.1	Ah-TARS4886-DRAFT-NextGenCassava-1.0	Contig	Cornell University	2023-04-10	10.0x	2.01 Gb

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

A novel thermotolerant l-rhamnose isomerase variant for biocatalytic conversion of d-allulose to d-allose

Sharma S, Patel SN, Singh SP

Appl Microbiol Biotechnol

02-Apr-2024

PMCID:	PMC10987364
doi:	10.1007/s00253-024-13074-w
PMID:	38564031

Green synthesis of silver nanoparticles and its environmental sensor ability to some heavy metals

Ibrahim NH, Taha GM, Hagaggi NS, Moghazy MA

BMC Chem

06-Jan-2024

PMCID:	PMC10771699
doi:	10.1186/s13065-023-01105-y
PMID:	38184656

The complete chloroplast genome and phylogenetic analysis of Acalypha hispida Burm. f. (Euphorbiaceae), an ornamental and medicinal plant

Dong Y, Du C, Yue J, Li W

Mitochondrial DNA B Resour

22-Nov-2023

PMCID:	PMC10769557
doi:	10.1080/23802359.2023.2284414
PMID:	38188445

Diversity, astaxanthin production, and genomic analysis of Rhodotorula paludigena SP9-15

Phuengjayaem S, Kingkaew E, Hoondee P, Rojsitthisak P, Sritularak B, Thitikornpong W, Thompho S, Pornputtapong N, Tanasupawat S

Heliyon

16-Jul-2023

PMCID:	PMC10395543
doi:	10.1016/j.heliyon.2023.e18280
PMID:	37539266

Anti-inflammatory potential of Penicillium brefeldianum endophytic fungus supported with phytochemical profiling

Saleh A, Negm WA, El-Masry TA, Eliwa D, Alotaibi B, Alosaimi ME, Alotaibi KN, Magdeldin S, Mahgoub S, Elekhnawy E

Microb Cell Fact

27-Apr-2023

PMCID:	PMC10141907
doi:	10.1186/s12934-023-02091-5
PMID:	37106372

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

Cross-School Collaboration to Develop and Implement Self-Construction Greening Systems for Schools

Teichmann F, Kirchengast I, Korjenic A

Plants (Basel)

10-Jan-2023

PMCID:	PMC9860625
doi:	10.3390/plants12020327
PMID:	36679040

A New Species of the Mealybug Genus Mirococcus (Hemiptera: Coccomorpha: Pseudococcidae) from the Cape Verde Islands, with New Records and an Updated Checklist of Scale Insect Species

Łagowska B, Golan K, Hodgson CJ

Insects

31-Oct-2022

PMCID:	PMC9697468
doi:	10.3390/insects13110999
PMID:	36354823

New Green Approaches in Nanoparticles Synthesis: An Overview

Miu BA, Dinischiotu A

Molecules

01-Oct-2022

PMCID:	PMC9573382
doi:	10.3390/molecules27196472
PMID:	36235008

Zinc Oxide Nanoparticles as Potential Delivery Carrier: Green Synthesis by Aspergillus niger Endophytic Fungus, Characterization, and In Vitro/In Vivo Antibacterial Activity

Abdelkader DH, Negm WA, Elekhnawy E, Eliwa D, Aldosari BN, Almurshedi AS

Pharmaceuticals (Basel)

26-Aug-2022

PMCID:	PMC9500724
doi:	10.3390/ph15091057
PMID:	36145278

Natural and Engineered Nanomaterials for the Identification of Heavy Metal Ions—A Review

Vonnie JM, Ting BJ, Rovina K, Aqilah NM, Yin KW, Huda N

Nanomaterials (Basel)

03-Aug-2022

PMCID:	PMC9370674
doi:	10.3390/nano12152665
PMID:	35957095

C4 trees have a broader niche than their close C3 relatives

Young SN, Dunning LT, Liu H, Stevens CJ, Lundgren MR

J Exp Bot

23-May-2022

PMCID:	PMC9126736
doi:	10.1093/jxb/erac113
PMID:	35293994

DNA Barcoding Medicinal Plant Species from Indonesia

Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N

Plants (Basel)

21-May-2022

PMCID:	PMC9147630
doi:	10.3390/plants11101375
PMID:	35631799

Cytobacts: Abundant and Diverse Vertically Seed-Transmitted Cultivation-Recalcitrant Intracellular Bacteria Ubiquitous to Vascular Plants

Thomas P, Rajendran TP, Franco CM

Front Microbiol

07-Mar-2022

PMCID:	PMC8967353
doi:	10.3389/fmicb.2022.806222
PMID:	35369514

Selected Natural Products in Neuroprotective Strategies for Alzheimer’s Disease—A Non-Systematic Review

Wojtunik-Kulesza K, Oniszczuk T, Mołdoch J, Kowalska I, Szponar J, Oniszczuk A

Int J Mol Sci

21-Jan-2022

PMCID:	PMC8835836
doi:	10.3390/ijms23031212
PMID:	35163136

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1002/1099-1573(200008)14:5<371::AID-PTR625>3.0.CO;2-F
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate	13250	Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O	198.17	unknown	https://doi.org/10.1002/1099-1573(200008)14:5<371::AID-PTR625>3.0.CO;2-F
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
3-Chloro-4-methoxybenzaldehyde	78619	Click to see COC1=C(C=C(C=C1)C=O)Cl	170.59	unknown	https://doi.org/10.1016/S0031-9422(03)00494-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
[(3S,3aR,4S,5aS,6R,9aR,9bS)-6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-2-oxo-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-4-yl] 3-methylbutanoate	15275720	Click to see CC1C2C(CC3(C(CCC(=C)C3(C2OC1=O)O)O)C)OC(=O)CC(C)C	366.40	unknown	https://doi.org/10.1016/S0031-9422(03)00494-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-galactoside	441699	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1016/S0031-9422(03)00494-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1002/1099-1573(200008)14:5<371::AID-PTR625>3.0.CO;2-F
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1002/1099-1573(200008)14:5<371::AID-PTR625>3.0.CO;2-F
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1R,19R,21S,22S,23S)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] (1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylate	162843720	Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)OC4C5COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC4C(C(O5)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)O)O)O)O)O	908.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
[(1R,7R,8R,26S,28S,29S,38R)-1,13,14,15,18,19,20,34,35,39,39-undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl] 3,4,5-trihydroxybenzoate	154496632	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
[(1R,7R,8R,26S,28S,29S)-1,13,14,15,18,19,20,34,35,39,39-undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl] 3,4,5-trihydroxybenzoate	163186467	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
[(1S,4S,5R,23S,25R,26R,36S,40R)-1,10,11,12,15,16,17,31,32-nonahydroxy-2,7,20,28,35,38-hexaoxo-3,6,21,24,27,34,37-heptaoxaoctacyclo[27.10.2.04,23.05,26.08,13.014,19.033,41.036,40]hentetraconta-8,10,12,14,16,18,29,31,33(41)-nonaen-25-yl] 3,4,5-trihydroxybenzoate	162988807	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(C(=O)O6)OC(=O)CC7(C(=O)O3)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
[(2R,3S,4R,5R,6S)-2,4,5-tris[(3,4,5-trihydroxybenzoyl)oxy]-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 2-[[(1R,7R,8R,26S,28R,29S,38R)-1,13,14,15,18,19,34,35,39,39-decahydroxy-2,5,10,23,30-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,31,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32(37),33,35-decaen-20-yl]oxy]-3,4,5-trihydroxybenzoate	154496548	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)C(=O)OC5=C6C7C(=CC(=O)C(C7(O)O)(OC6=C(C(=C5)O)O)O)C(=O)O3)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	1891.30	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
[(2R,3S,4R,5S,6R)-3,4,5-tris[(3,4,5-trihydroxybenzoyl)oxy]-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl] 2-[[(1S,7S,8R,26R,28S,29R,38R)-1,13,14,15,18,20,34,35,39,39-decahydroxy-2,5,10,23,30-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,31,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32(37),33,35-decaen-19-yl]oxy]-3,4,5-trihydroxybenzoate	159449526	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)C(=O)OC5=C6C7C(=CC(=O)C(C7(O)O)(OC6=C(C(=C5)O)O)O)C(=O)O3)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(C(O1)COC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O	1891.30	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
[(4S,5R,23S,25R,26R,36S,40R)-1,10,11,12,15,16,17,31,32-nonahydroxy-2,7,20,28,35,38-hexaoxo-3,6,21,24,27,34,37-heptaoxaoctacyclo[27.10.2.04,23.05,26.08,13.014,19.033,41.036,40]hentetraconta-8,10,12,14,16,18,29,31,33(41)-nonaen-25-yl] 3,4,5-trihydroxybenzoate	163195226	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(C(=O)O6)OC(=O)CC7(C(=O)O3)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
Acalyphidin D1	154496094	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C8C(C(C(O7)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C4=C2C2C(=CC(=O)C(C2(O4)O)(O)O)C(=O)O8)O)O)OC(=O)C2=CC(=C(C(=C26)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C4=C2C2C(=CC(=O)C(C2(O4)O)(O)O)C(=O)O3)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1903.30	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
CID 338147	338147	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1002/1099-1573(200008)14:5<371::AID-PTR625>3.0.CO;2-F
Euphorbin B (a form)	16133907	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O.C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O6)O)(O)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	3782.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
Euphorbin B (b form)	16197485	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(=O)C7(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
Mallotusinin	514180	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7=C(O6)C(=C(C=C7C(=O)O3)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	918.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2
Phyllanthusiin C	514181	Click to see C1C(C2(C3C1(C(=O)OC4C5COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC4C(C(O5)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C39)O2)O)O)O)O)O)O)O)O)O)O)O	926.60	unknown	https://doi.org/10.1016/S0031-9422(98)00579-2

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Acalypha hispida

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