Scientific name	Authority	First published in
Conyza appendiculata	Blume	Bijdr. Fl. Ned. Ind. 15: 895 (1826)
Conyza balsamifera	L.	Sp. Pl. , ed. 2, 2: 1208 (1763)
Conyza vestita	Wall.	Numer. List : n.° 2998 (1831)
Blumea zollingeriana	C.B.Clarke	Compos. Ind. : 90 (1876)
Baccharis salvia	Lour.	Fl. Cochinch. 2: 494 (1790)
Blumea grandis	DC.	Prodr. 5: 447 (1836)
Pluchea balsamifera	Less.	Linnaea 6: 150 (1831)
Placus balsamifer	Baill.	Hist. Pl. 8: 303 (1882)
Baccharis balsamifera	Stokes	Bot. Mat. Med. 4: 204 (1812)
Blumea balsamifera var. microcephala	Kitam.	Acta Phytotax. Geobot. 23: 66 (1968)
Conyza grandis	Wall.	Numer. List : n.° 3051 (1831)

Common names Top

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Filter by language:

Language	Common/alternative name
English	ngai camphor
Spanish	conyza saxatilis
Spanish	baccharis gratissima
Spanish	pluchea appendiculata
ace	capa
ban	sembung
bcl	lakad-bulan
French	sambong
Indonesian	sembung
min	capo
Malay	pokok sembung
Burmese	ဘုမ္မသိန်ပင်
Oriya	ପୋକଶୁଙ୍ଗା
pam	sambung
pwn	karuveljevelj
Thai	หนาด
Vietnamese	Đại bi
Chinese	艾纳香根
Chinese	艾纳香
Chinese	艾納香
Chinese	艾片
Chinese	牛大艾
Chinese	大风艾

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Africa click to expand
- West-central Tropical Africa
  - Zaïre

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Christmas Island
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000002804
UNII	HK4UMV6L8F
USDA Plants	BLBA2
Tropicos	2701935
KEW	urn:lsid:ipni.org:names:185502-1
The Plant List	gcc-102702
Open Tree Of Life	137907
NCBI Taxonomy	313920
IUCN Red List	147637227
IPNI	185502-1
iNaturalist	347625
GBIF	5395786
Freebase	/m/09rtmd0
EPPO	BLUBA
EOL	482126
USDA GRIN	7276
Wikipedia	Blumea_balsamifera

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

Polyphenols of the Inuleae-Inulinae and Their Biological Activities: A Review

Malarz J, Michalska K, Stojakowska A

Molecules

27-Apr-2024

PMCID:	PMC11085778
doi:	10.3390/molecules29092014
PMID:	38731504

Green Preparation and Antibacterial Activity Evaluation of AgNPs-Blumea balsamifera Oil Nanoemulsion

Ma C, Liu B, Du L, Liu W, Zhu Y, Chen T, Wang Z, Chen H, Pang Y

Molecules

26-Apr-2024

PMCID:	PMC11085303
doi:	10.3390/molecules29092009
PMID:	38731501

Green Synthesis of Blumea balsamifera Oil Nanoemulsions Stabilized by Natural Emulsifiers and Its Effect on Wound Healing

Du L, Ma C, Liu B, Liu W, Zhu Y, Wang Z, Chen T, Huang L, Pang Y

Molecules

26-Apr-2024

PMCID:	PMC11085480
doi:	10.3390/molecules29091994
PMID:	38731484

Characterization of Bioactive Metabolites and Antioxidant Activities in Solid and Liquid Fractions of Fresh Duckweed (Wolffia globosa) Subjected to Different Cell Wall Rupture Methods

Yadav NK, Patel AB, Debbarma S, Priyadarshini MB, Priyadarshi H

ACS Omega

23-Apr-2024

PMCID:	PMC11080017
doi:	10.1021/acsomega.3c09674
PMID:	38737040

Molecular Structure, Antioxidant Potential, and Pharmacokinetic Properties of Plant Flavonoid Blumeatin and Investigating Its Inhibition Mechanism on Xanthine Oxidase for Hyperuricemia by Molecular Modeling

Altunayar-Unsalan C, Unsalan O

ACS Omega

11-Mar-2024

PMCID:	PMC10956095
doi:	10.1021/acsomega.3c10083
PMID:	38524493

Use of Medicinal Plants in the Process of Wound Healing: A Literature Review

Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL

Pharmaceuticals (Basel)

27-Feb-2024

PMCID:	PMC10975678
doi:	10.3390/ph17030303
PMID:	38543089

Full-Length Transcriptome Sequencing and RNA-Seq Analysis Offer Insights into Terpenoid Biosynthesis in Blumea balsamifera (L.) DC.

Ju Z, Liang L, Zheng Y, Shi H, Zhao W, Sun W, Pang Y

Genes (Basel)

24-Feb-2024

PMCID:	PMC10970515
doi:	10.3390/genes15030285
PMID:	38540346

Integrated water management practice in tropical peatland agriculture has low carbon emissions and subsidence rates

Fawzi NI, Sumawinata B, Suwardi, Rahmasary AN, Qurani IZ, Naufaldary RG, Nabillah R, Palunggono HB, Mulyanto B

Heliyon

21-Feb-2024

PMCID:	PMC10912239
doi:	10.1016/j.heliyon.2024.e26661
PMID:	38444506

Formulation of Mentha piperita-Based Nanobiopesticides and Assessment of the Pesticidal and Antimicrobial Potential

Jahan N, Hussain N, Touqeer SI, KU, Shamshad H, Abbas N

Life (Basel)

19-Jan-2024

PMCID:	PMC10817515
doi:	10.3390/life14010144
PMID:	38276273

A critical overview of challenging roles of medicinal plants in improvement of wound healing technology

Pathak D, Mazumder A

Daru

15-Jan-2024

PMCID:	PMC11087437
doi:	10.1007/s40199-023-00502-x
PMID:	38225520

Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China

Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y

J Ethnobiol Ethnomed

02-Jan-2024

PMCID:	PMC10763305
doi:	10.1186/s13002-023-00645-w
PMID:	38169414

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

A comparative analysis of morphology, microstructure, and volatile metabolomics of leaves at varied developmental stages in Ainaxiang (Blumea balsamifera (Linn.) DC.)

Chen X, Li Y, Pang Y, Shen W, Chen Q, Liu L, Luo X, Chen Z, Li X, Li Y, Zhang Y, Huang M, Yuan C, Wang D, Guan L, Liu Y, Yang Q, Chen H, Wu H, Yu F

Front Plant Sci

14-Nov-2023

PMCID:	PMC10682096
doi:	10.3389/fpls.2023.1285616
PMID:	38034556

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

Research progress on the regulation and mechanism of borneol on the blood-brain barrier in pathological states: a narrative review focused on ischemic stroke and cerebral glioma

Tan X, Zhang K, Shi W, Tang Z

Transl Cancer Res

22-Oct-2023

PMCID:	PMC10731338
doi:	10.21037/tcr-23-1487
PMID:	38130309

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 / Diterpenoids
3,4a,8,8-tetramethyl-4-(3-methylpenta-2,4-dienyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,2,3-triol	72975030	Click to see CC(=CCC1C2(CCCC(C2C(C(C1(C)O)O)O)(C)C)C)C=C	322.50	unknown	https://doi.org/10.1021/NP100646N
Austroinulin	11472742	Click to see CC(=CCC1C2(CCCC(C2C(C(C1(C)O)O)O)(C)C)C)C=C	322.50	unknown	https://doi.org/10.1021/NP100646N
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
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/10.1021/NP100646N
Proximadiol	165258	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1021/NP100646N
Samboginone, (rel)-	52936973	Click to see CC1=C2C(=O)C(CC(C2(C(=O)CC1)C)O)C(C)C	250.33	unknown	https://doi.org/10.1021/NP100646N
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(10-Hydroxy-6,10-dimethyl-4,9-dioxo-3-propan-2-ylcyclodec-5-en-1-yl) 2,3-dimethyloxirane-2-carboxylate	72802307	Click to see CC1C(O1)(C)C(=O)OC2CC(C(=O)C=C(CCC(=O)C2(C)O)C)C(C)C	366.40	unknown	https://doi.org/10.1021/NP049622E
[(1R,3R,5E,10S)-10-hydroxy-6,10-dimethyl-4,9-dioxo-3-propan-2-ylcyclodec-5-en-1-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate	163082386	Click to see CC1C(O1)(C)C(=O)OC2CC(C(=O)C=C(CCC(=O)C2(C)O)C)C(C)C	366.40	unknown	https://doi.org/10.1021/NP049622E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3a,4-Dihydroxy-4-methyl-1-methylidene-8-oxo-7-propan-2-yl-2,3,5,6,7,8a-hexahydroazulen-5-yl) 2-methylbut-2-enoate	72806719	Click to see CC=C(C)C(=O)OC1CC(C(=O)C2C(=C)CCC2(C1(C)O)O)C(C)C	350.40	unknown	https://doi.org/10.1021/NP049622E
[(3aS,4R,5R,7S)-3a,4-dihydroxy-1,4-dimethyl-8-oxo-7-propan-2-yl-3,5,6,7-tetrahydro-2H-azulen-5-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate	162954925	Click to see CC1C(O1)(C)C(=O)OC2CC(C(=O)C3=C(CCC3(C2(C)O)O)C)C(C)C	366.40	unknown	https://doi.org/10.1021/NP100646N
[(3aS,4R,5S,7S,8aR)-3a,4-dihydroxy-4-methyl-1-methylidene-8-oxo-7-propan-2-yl-2,3,5,6,7,8a-hexahydroazulen-5-yl] (Z)-2-methylbut-2-enoate	163190022	Click to see CC=C(C)C(=O)OC1CC(C(=O)C2C(=C)CCC2(C1(C)O)O)C(C)C	350.40	unknown	https://doi.org/10.1021/NP049622E
[(3aS,4R,5S,7S)-3a,4-dihydroxy-1,4-dimethyl-8-oxo-7-propan-2-yl-3,5,6,7-tetrahydro-2H-azulen-5-yl] (2S,3S)-2,3-dihydroxy-2-methylbutanoate	162933369	Click to see CC1=C2C(=O)C(CC(C(C2(CC1)O)(C)O)OC(=O)C(C)(C(C)O)O)C(C)C	384.50	unknown	https://doi.org/10.1021/NP100646N
Blumeaene E1	52936861	Click to see CC1C(O1)(C)C(=O)OC2CC(C(=O)C3=C(CCC3(C2(C)O)O)C)C(C)C	366.40	unknown	https://doi.org/10.1021/NP100646N
Blumeaene E2	52936862	Click to see CC1C(O1)(C)C(=O)OC2CC(C(=O)C3=C(CCC3(C2(C)O)O)C)C(C)C	366.40	unknown	https://doi.org/10.1021/NP100646N
Blumeaene L	52936971	Click to see CC1=C2C(=O)C(CC(C(C2(CC1)O)(C)O)OC(=O)C)C(C)C	310.40	unknown	https://doi.org/10.1021/NP100646N
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2-Hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl) 3-methylbut-2-enoate	162944493	Click to see CC1CCCC2(C(O2)C(C3C(C1OC(=O)C=C(C)C)OC(=O)C3=C)O)C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1R,2R,3R,5R,9R,10R,11R)-2-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl] 3-methylbut-2-enoate	162944494	Click to see CC1CCCC2(C(O2)C(C3C(C1OC(=O)C=C(C)C)OC(=O)C3=C)O)C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1R,2R,3R,5R,9R,10R,11R)-2-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl] acetate	14021262	Click to see CC1CCCC2(C(O2)C(C3C(C1OC(=O)C)OC(=O)C3=C)O)C	324.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1R,2R,3R,5R,9R,10R,11S)-2-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl] acetate	162916296	Click to see CC1CCCC2(C(O2)C(C3C(C1OC(=O)C)OC(=O)C3=C)O)C	324.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1R,2R,3R,5S,9R,10S,11S)-2-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl] acetate	101618007	Click to see CC1CCCC2(C(O2)C(C3C(C1OC(=O)C)OC(=O)C3=C)O)C	324.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1S,2R,3R,5R,9R,10R,11R)-10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-2-yl] (Z)-2-methylbut-2-enoate	162897652	Click to see CC=C(C)C(=O)OC1C2C(C(C(CCCC3(C1O3)C)C)O)OC(=O)C2=C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1S,2R,3R,5R,9R,10R,11S)-10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-2-yl] (Z)-2-methylbut-2-enoate	162897653	Click to see CC=C(C)C(=O)OC1C2C(C(C(CCCC3(C1O3)C)C)O)OC(=O)C2=C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
[(1S,2R,3R,5R,9R,10R,11S)-10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-2-yl] 3-methylbut-2-enoate	162856598	Click to see CC1CCCC2(C(O2)C(C3C(C1O)OC(=O)C3=C)OC(=O)C=C(C)C)C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
2-Butenoic acid, 2-methyl-, (1aR,5R,6R,6aS,9aS,10R,10aR)-dodecahydro-6-hydroxy-1a,5-dimethyl-9-methylene-8-oxooxireno[4,5]cyclodeca[1,2-b]furan-10-yl ester, (2Z)-	162897651	Click to see CC=C(C)C(=O)OC1C2C(C(C(CCCC3(C1O3)C)C)O)OC(=O)C2=C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
Blumealactone B	14021258	Click to see CC1CCCC2(C(O2)C(C3C(C1O)OC(=O)C3=C)OC(=O)C=C(C)C)C	364.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
Blumealactone C	14021261	Click to see CC1CCCC2(C(O2)C(C3C(C1OC(=O)C)OC(=O)C3=C)O)C	324.40	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5S,6R)-2-[(2S)-4-[(1R,2S,4S,7S,8R,9S,12S,13S,15R,16R,18S)-6,15-dihydroxy-7,9,13-trimethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10581588	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	907.00	unknown	https://doi.org/10.1016/0031-9422(88)80284-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-3-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-5,7-dihydroxychromen-4-one	163022606	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC(=C(C=C6)O)O)O)O)O	570.50	unknown	https://doi.org/10.1016/J.FITOTE.2004.10.015
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,2'-Trihydroxy-7,5'-dimethoxyflavone	44258717	Click to see COC1=CC(=C(C=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O	330.29	unknown	https://doi.org/10.1016/S0031-9422(00)97584-8
Rhamnazin	5320945	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)OC)O	330.29	unknown	https://doi.org/10.1016/J.FITOTE.2004.10.015
Tamarixetin	5281699	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.1021/NP100646N
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Dihydrotamarixetin	11666859	Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	318.28	unknown	https://doi.org/10.1021/NP049622E
Dihydrotamarixetin	482576	Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	318.28	unknown	https://doi.org/10.1021/NP049622E
Quercetin 3,4'-dimethyl ether	5380905	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O	330.29	unknown	https://doi.org/10.1021/NP049622E
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2r,3r)-3,5,2'-Trihydroxy-7,5'-dimethoxyflavanone	129710934	Click to see COC1=CC(=C(C=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)OC)O)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(00)97584-8
2',3,5-Trihydroxy-5',7-dimethoxyflavanone	131752832	Click to see COC1=CC(=C(C=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)OC)O)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(00)97584-8
3,3',5-Trihydroxy-4',7-dimethoxyflavanone	11256019	Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)OC)O)O)O	332.30	unknown	https://doi.org/10.1021/NP049622E
3,7-Di-O-methylquercetin	5280417	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O	330.29	unknown	https://doi.org/10.1021/NP049622E
7-O-Methyleriodictyol	1268276	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1021/NP049622E
7-O-Methylluteolin	5318214	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1021/NP049622E https://doi.org/10.1016/J.FITOTE.2004.10.015
Ayanin	5280682	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O	344.30	unknown	https://doi.org/10.1021/NP049622E
Blumeatin B	157600	Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)OC)O)O)O	332.30	unknown	https://doi.org/10.1021/NP049622E
Pachypodol	5281677	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	344.30	unknown	https://doi.org/10.1021/NP049622E
Sternbin	4872981	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1021/NP049622E
Velutin	5464381	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O	314.29	unknown	https://doi.org/10.1021/NP049622E

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Blumea balsamifera

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