Afrocarpus falcatus

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID644007bed1056068128799
Scientific name	Afrocarpus falcatus
Authority	(Thunb.) C.N.Page
First published in	Notes Roy. Bot. Gard. Edinburgh 45: 383 (1988 publ. 1989)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Nageia meyeriana	Kuntze	Revis. Gen. Pl. 2: 800 (1891)
Nageia falcata var. gaussenii	(Woltz) Silba	J. Int. Conifer Preserv. Soc. 7: 27 (2000)
Nageia falcata	Carrière	Rev. Hort. (Paris) 41: 370 (1869)
Taxus falcata	Thunb.	Prodr. Pl. Cap. : 117 (1800)
Podocarpus gracillimus	Stapf	Fl. Trop. Afr. 6(2): 343 (1917)
Podocarpus gaussenii	Woltz	Trav. Lab. Forest. Toulouse 1(8)2: 6 (1970)
Podocarpus falcatus	A.Cunn. ex Parl.	Prodr. [A. P. de Candolle] 16(2.2): 517. 1868 [mid Jul 1868]
Podocarpus meyerianus	Endl.	Syn. Conif. : 218 (1847)
Afrocarpus gaussenii	(Woltz) C.N.Page	Notes Roy. Bot. Gard. Edinburgh 45: 384 (1988 publ. 1989)
Decussocarpus falcatus	(Thunb.) de Laub.	J. Arnold Arbor. 50: 359 (1969)
Afrocarpus falcatus subsp. gaussenii	(Woltz) Silba	J. Int. Conifer Preserv. Soc. 17: 21 (2010)
Podocarpus falcatus	R.Br. ex Mirb.	Mém. Mus. Hist. Nat. 13: 75. 1825

Common names Top

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Filter by language:

Language	Common/alternative name
English	yellowwood
English	bastard yellowwood
English	outeniqua yellowwood
Afrikaans	kalandergeelhout
Afrikaans	outeniekwageelhout
German	gewöhnliches afrogelbholz
Persian	چوبزرد معمولی
Dutch	kalander
Dutch	outeniquageelhout
Chinese	镰叶非洲杉
Chinese	非洲杉
Chinese	镰形罗汉松
Chinese	鐮形羅汉松
Chinese	镰叶罗汉松

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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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
- Middle Atlantic Ocean
  - Saint Helena
- South Tropical Africa
  - Malawi
  - Mozambique
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland
- Western Indian Ocean
  - Madagascar

Australasia click to expand
- Australia
  - New South Wales

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000522640
USDA Plants	AFFA
Tropicos	25600067
KEW	urn:lsid:ipni.org:names:946473-1
The Plant List	kew-2624884
Open Tree Of Life	207209
NCBI Taxonomy	56897
IUCN Red List	42438
IPNI	946473-1
iNaturalist	136323
GBIF	2687632
Freebase	/m/026v2gn
EPPO	PODFA
EOL	1033604
USDA GRIN	403361
Wikipedia	Afrocarpus_falcatus
CMAUP	NPO10241

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

Modeling habitat suitability for the lesser‐known populations of endangered mountain nyala (Tragelaphus buxtoni) in the Arsi and Ahmar Mountains, Ethiopia

Worku EA, Evangelista PH, Atickem A, Bekele A, Bro‐Jørgensen J, Stenseth NC

Ecol Evol

15-Apr-2024

PMCID:	PMC11017409
doi:	10.1002/ece3.11235
PMID:	38623519

Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia

Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A

J Ethnobiol Ethnomed

09-Mar-2024

PMCID:	PMC10924356
doi:	10.1186/s13002-024-00665-0
PMID:	38461267

Medicinal Plants Used by Oromo Community in Kofale District, West-Arsi Zone, Oromia Regional State, Ethiopia

Nuro GB, Tolossa K, Giday M

J Exp Pharmacol

05-Mar-2024

PMCID:	PMC10929209
doi:	10.2147/JEP.S449496
PMID:	38476311

Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia

Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW

J Ethnobiol Ethnomed

28-Feb-2024

PMCID:	PMC10900619
doi:	10.1186/s13002-024-00666-z
PMID:	38419092

Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia

Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A

J Ethnobiol Ethnomed

22-Feb-2024

PMCID:	PMC10885532
doi:	10.1186/s13002-024-00651-6
PMID:	38389077

Diurnal activity time budget of Grevy's zebra (Equus grevyi, Oustalet 1882) in a protected savannah area

Abriham T, Bekele A, Yihune M

Heliyon

09-Feb-2024

PMCID:	PMC10869900
doi:	10.1016/j.heliyon.2024.e26117
PMID:	38370237

Biodiversity and Structural Analysis of Woody Plant Species of Home Gardens in Basona Worana District, North Shoa Zone of Central Ethiopia

Woldeyohannes A, Moges A

Scientifica (Cairo)

08-Feb-2024

PMCID:	PMC10869191
doi:	10.1155/2024/5563636
PMID:	38361969

Species composition, relative abundance, and habitat association of birds in Dodola dry evergreen afro-montane forest and sub-afro-alpine scrubland vegetation, southeast Ethiopia

Yilma ZA, Mengesha G, Girma Z

PeerJ

11-Jan-2024

PMCID:	PMC10788088
doi:	10.7717/peerj.16775
PMID:	38223764

Ethnobotanical study of traditional medicinal plants used by the local people in Habru District, North Wollo Zone, Ethiopia

Alemu M, Asfaw Z, Lulekal E, Warkineh B, Debella A, Sisay B, Debebe E

J Ethnobiol Ethnomed

04-Jan-2024

PMCID:	PMC10768247
doi:	10.1186/s13002-023-00644-x
PMID:	38178202

Medicinal Plants in Treating Hepatitis B Among Communities of Central Region of Ethiopia

Beykaso G, Teklehaymanot T, Mulu A, Berhe N, Alemayehu DH, Giday M

Hepat Med

29-Dec-2023

PMCID:	PMC10759923
doi:	10.2147/HMER.S440351
PMID:	38170153

Traditional homegardens change to perennial monocropping of khat (Catha edulis) reduced woody species and enset conservation and climate change mitigation potentials of the Wondo Genet landscape of southern Ethiopia

Mellisse BT, Tolera M, Derese A

Heliyon

13-Dec-2023

PMCID:	PMC10770471
doi:	10.1016/j.heliyon.2023.e23631
PMID:	38187286

Remote sensing and GIS-based study of land use/cover dynamics, driving factors, and implications in southern Ethiopia, with special reference to the Legabora watershed

Mariye M, Jianhua L, Maryo M, Tsegaye G, Aletaye E

Heliyon

07-Dec-2023

PMCID:	PMC10750153
doi:	10.1016/j.heliyon.2023.e23380
PMID:	38148827

Ethnobotanical Study on Medicinal Plants Used by the Local Communities of Ameya District, Oromia Regional State, Ethiopia

Tadesse T, Teka A

Evid Based Complement Alternat Med

01-Dec-2023

PMCID:	PMC10708956
doi:	10.1155/2023/5961067
PMID:	38074846

Ethnobotanical study on medicinal plant knowledge among three ethnic groups in peri-urban areas of south-central Ethiopia

Tamene S, Negash M, Makonda FB, Chiwona-Karltun L, Kibret KS

J Ethnobiol Ethnomed

23-Nov-2023

PMCID:	PMC10668360
doi:	10.1186/s13002-023-00629-w
PMID:	37996915

Detailed Seed Cone Morpho-Anatomy Provides New Insights into Seed Cone Origin and Evolution of Podocarpaceae; Podocarpoid and Dacrydioid Clades

Khan R, Hill RS, Dörken VM, Biffin E

Plants (Basel)

19-Nov-2023

PMCID:	PMC10674377
doi:	10.3390/plants12223903
PMID:	38005800

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aS,10aR)-6-[(4bS,8S,8aR)-8-carboxy-2-hydroxy-4b,8-dimethyl-1-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]-7-hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	12312652	Click to see CC(C)C1=C(C(=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)C4=CC5=C(CCC6C5(CCCC6(C)C(=O)O)C)C(=C4O)C(C)C)O	630.90	unknown	https://doi.org/10.1016/S0031-9422(00)80328-3
(1S,4aS)-6-[(4bS,8S)-8-carboxy-2-hydroxy-4b,8-dimethyl-1-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]-7-hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	5319165	Click to see CC(C)C1=C(C(=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)C4=CC5=C(CCC6C5(CCCC6(C)C(=O)O)C)C(=C4O)C(C)C)O	630.90	unknown	https://doi.org/10.1016/S0031-9422(00)80328-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone	44260067	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC)OC	376.30	unknown	via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone	14483219	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC)O	362.30	unknown	via CMAUP database
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Limocitrol	12311234	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O)O	376.30	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	13871824	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)O)O	432.40	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	57511421	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	via CMAUP database
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin	5318644	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone	5319442	Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O	316.26	unknown	via CMAUP database
Gossypetin 3-methyl ether	5386958	Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC(=C(C=C3)O)O	332.26	unknown	via CMAUP database
Gossypetin 3,3'-dimethyl ether	21676153	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)OC)O	346.30	unknown	via CMAUP database
Quercetagetin 3-methyl ether	5320475	Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O	332.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone	5352032	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	330.29	unknown	via CMAUP database
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone	44259895	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O)OC	390.30	unknown	via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone	44258045	Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	390.30	unknown	via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone	44258041	Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	376.30	unknown	via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone	44259884	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)O)O)O)O	362.30	unknown	via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone	21676156	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O	362.30	unknown	via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone	44260054	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)O)O	346.30	unknown	via CMAUP database
Axillarin	5281603	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O	346.30	unknown	via CMAUP database
Jaceidin	5464461	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin	44259900	Click to see COC1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)OC)OC	432.40	unknown	via CMAUP database
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone	5748553	Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O	346.30	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6,8-trimethoxy-	5386960	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)O	360.30	unknown	via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone	44260077	Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC	448.40	unknown	via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone	44260086	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O)OC	434.40	unknown	via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone	369954	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O	404.40	unknown	via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone	54799	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC	390.30	unknown	via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone	44260074	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O	420.40	unknown	via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone	100625	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O	404.40	unknown	via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone	44260073	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O	406.30	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one	5386959	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	390.30	unknown	via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone	5386963	Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC	434.40	unknown	via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone	5487077	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC	420.40	unknown	via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone	21676158	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)O	406.30	unknown	via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone	44260043	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O	376.30	unknown	via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone	44258626	Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O	346.30	unknown	via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone	44260085	Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	406.30	unknown	via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone	21599528	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	390.30	unknown	via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone	5352085	Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC	420.40	unknown	via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone	5386962	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)O	376.30	unknown	via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone	44260072	Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC	406.30	unknown	via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone	11383767	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)O)O)OC)OC)O	392.30	unknown	via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone	44260071	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	406.30	unknown	via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone	21676159	Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC	420.40	unknown	via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone	13983738	Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O	330.29	unknown	via CMAUP database
Agecorynin D	14162688	Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O	390.30	unknown	via CMAUP database
Calycopterin	10429470	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC	374.30	unknown	via CMAUP database
Conyzatin	13916282	Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC	404.40	unknown	via CMAUP database
Digicitrin	10071564	Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC	434.40	unknown	via CMAUP database
Gossypetin 3,8,3'-trimethyl ether	5386961	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O	360.30	unknown	via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether	44260037	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O	376.30	unknown	via CMAUP database

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Afrocarpus falcatus

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