Holarrhena floribunda

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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	UUID64403e55d89a8340193290
Scientific name	Holarrhena floribunda
Authority	T.Durand & Schinz
First published in	Mém. Couronnés Autres Mém. Acad. Roy. Sci. Belgique 53: 190 (1896)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Rondeletia floribunda	G.Don	Gen. Hist. 3: 516 (1834)
Holarrhena africana	A.DC.	Prodr. 8: 414 (1844)
Holarrhena floribunda var. tomentella	H.Huber	Kew Bull. 15: 437. 1962
Holarrhena ovata	A.DC.	Prodr. 8: 414 (1844)
Holarrhena wulfsbergii	Stapf	Fl. Trop. Afr. 4(1): 164 (1902)

Common names Top

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Language	Common/alternative name
English	false rubber tree
Fulah	nyiiwahi

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
- Northeast Tropical Africa
  - Chad
  - Sudan
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Mali
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Cabinda
  - Cameroon
  - Central African Republic
  - Congo
  - Gabon
  - Zaïre

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000982764
USDA Plants	HOFL2
Tropicos	1805621
KEW	urn:lsid:ipni.org:names:79302-1
The Plant List	kew-99606
Open Tree Of Life	3870702
NCBI Taxonomy	2708850
IUCN Red List	144299547
IPNI	79302-1
iNaturalist	505792
GBIF	3169751
Freebase	/m/0wxrn5g
EPPO	HRHFL
EOL	483924
USDA GRIN	70358
Wikipedia	Holarrhena_floribunda
CMAUP	NPO12483

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

Allometric relationships between stem diameter, height and crown area of associated trees of cocoa agroforests of Ghana

Asigbaase M, Dawoe E, Abugre S, Kyereh B, Ayine Nsor C

Sci Rep

09-Sep-2023

PMCID:	PMC10492788
doi:	10.1038/s41598-023-42219-6
PMID:	37689748

Biological Activity and Structural Diversity of Steroids Containing Aromatic Rings, Phosphate Groups, or Halogen Atoms

Dembitsky VM

Molecules

20-Jul-2023

PMCID:	PMC10384810
doi:	10.3390/molecules28145549
PMID:	37513423

Ethnobotanical Survey and Cercaricidal Activity Screening of Medicinal Plants Used for Schistosomiasis Treatment in Atwima-Nwabiagya District, Ashanti Region, Ghana

Asante-Kwatia E, Gyimah L, Forkuo AD, Anyan WK, Gbemu MA, Armah FA, Mensah AY

J Parasitol Res

19-Jul-2023

PMCID:	PMC10372336
doi:	10.1155/2023/6707157
PMID:	37520159

Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau

Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P

Plants (Basel)

08-May-2023

PMCID:	PMC10181441
doi:	10.3390/plants12091909
PMID:	37176967

Phytochemicals as Invaluable Sources of Potent Antimicrobial Agents to Combat Antibiotic Resistance

Jadimurthy R, Jagadish S, Nayak SC, Kumar S, Mohan CD, Rangappa KS

Life (Basel)

04-Apr-2023

PMCID:	PMC10145550
doi:	10.3390/life13040948
PMID:	37109477

Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides

Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH

Life (Basel)

11-Nov-2022

PMCID:	PMC9696702
doi:	10.3390/life12111852
PMID:	36430987

Chemistry and bioactivities of natural steroidal alkaloids

Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD

Nat Prod Bioprospect

15-Jun-2022

PMCID:	PMC9198197
doi:	10.1007/s13659-022-00345-0
PMID:	35701630

Latitudinal variation in the woody species diversity and population structure of Lannea microcarpa Engl. and K. Krause in Burkina Faso

Tinguéri B, Dimobe K, Lankoandé B, Boussim JI, Ouédraogo A

Heliyon

04-Jun-2022

PMCID:	PMC9192807
doi:	10.1016/j.heliyon.2022.e09625
PMID:	35711998

Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa

Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT

Plants (Basel)

23-May-2022

PMCID:	PMC9143319
doi:	10.3390/plants11101387
PMID:	35631812

Traditional Medicine Utilisation Among Pregnant Women in Sub-saharan African Countries: A Systematic Review of Literature

Mudonhi N, Nunu WN

Inquiry

04-May-2022

PMCID:	PMC9073130
doi:	10.1177/00469580221088618
PMID:	35506677

Escaping mechanisms of ESKAPE pathogens from antibiotics and their targeting by natural compounds

Jadimurthy R, Mayegowda SB, Nayak SC, Mohan CD, Rangappa KS

Biotechnol Rep (Amst)

04-Apr-2022

PMCID:	PMC9171455
doi:	10.1016/j.btre.2022.e00728
PMID:	35686013

Hydro-ethanol extract of Holarrhena floribunda stem bark exhibits anti-anaphylactic and anti-oedematogenic effects in murine models of acute inflammation

Antwi S, Oduro-Mensah D, Obiri DD, Osafo N, Antwi AO, Ansah HO, Ocloo A, Okine LK

BMC Complement Med Ther

19-Mar-2022

PMCID:	PMC8934059
doi:	10.1186/s12906-022-03565-6
PMID:	35305615

Prophylactic or therapeutic administration of Holarrhena floribunda hydro ethanol extract suppresses complete Freund’s adjuvant-induced arthritis in Sprague-Dawley rats

Antwi S, Oduro-Mensah D, Asiedu-Larbi J, Oduro-Mensah E, Quasie O, Lewis C, Darko-Obiri D, Ocloo A, Okine LK

J Inflamm (Lond)

05-Mar-2022

PMCID:	PMC8897772
doi:	10.1186/s12950-022-00301-2
PMID:	35248062

Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants

Ajao AA, Mukaila YO, Sabiu S

Heliyon

25-Dec-2021

PMCID:	PMC8733184
doi:	10.1016/j.heliyon.2021.e08668
PMID:	35024488

In Silico Approaches to Identify Polyphenol Compounds as α-Glucosidase and α-Amylase Inhibitors against Type-II Diabetes

Riyaphan J, Pham DC, Leong MK, Weng CF

Biomolecules

14-Dec-2021

PMCID:	PMC8699780
doi:	10.3390/biom11121877
PMID:	34944521

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
> Alkaloids and derivatives / Aporphines
(+)-1,2-Methylenedioxy-5,6,6aalpha,7-tetrahydro-4H-dibenzo[de,g]quinoline	26202781	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline	1078819	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC	355.40	unknown	via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone	10246449	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3	337.40	unknown	via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)-	158516	Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O	293.30	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
Lanuginosine	97622	Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	305.30	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
N-acetylanonaine	6453733	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	307.30	unknown	via CMAUP database
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol	15560530	Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O	281.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl-	11857938	Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C	280.40	unknown	via CMAUP database
4-O-Methylhonokiol	155160	Click to see COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C	280.40	unknown	via CMAUP database
Caryolanemagnolol	21726647	Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C	486.70	unknown	via CMAUP database
Honokiol	72303	Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C=C2)O)CC=C	266.30	unknown	via CMAUP database
Magnaldehyde E	5319190	Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O	254.28	unknown	via CMAUP database
Magnolol	72300	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O	266.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde	71812224	Click to see C=CCC1=CC=C(C=C1)OC2=C(C(=C(C(=C2)C=O)O)O)O	286.28	unknown	via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal	134367	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde	23259953	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=O	270.28	unknown	via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol	71812222	Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O	312.40	unknown	via CMAUP database
Obovatal	6439677	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
Obovatol	100771	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C	282.30	unknown	via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)-	10016628	Click to see C=CCC1=CC(=C(C=C1)OC2=CC(=C(C=C2)CC=C)O)O	282.30	unknown	via CMAUP database
Phenol, 4-(2-propenyl)-2-(4-(2-propenyl)phenoxy)-	159137	Click to see C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O	266.30	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol	68148	Click to see C=CCC1=CC=C(C=C1)O	134.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5R,9S,10R,13R)-5-(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	162895688	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(CO)C(=O)O	318.40	unknown	https://doi.org/10.1021/NP990332L
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
Cadalene	10225	Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C	198.30	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Clovanemagnolol	10323149	Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C	486.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol	91730386	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol	118976561	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	via CMAUP database
Eudeshonokiol A	14587421	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)C4=C(C=CC(=C4)CC=C)O)CC=C	488.70	unknown	via CMAUP database
Eudeshonokiol B	21726646	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=CC(=C(C=C4)O)CC=C	488.70	unknown	via CMAUP database
Eudesmagnolol	14587417	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O	488.70	unknown	via CMAUP database
Eudesobovatol A	442837	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C	504.70	unknown	via CMAUP database
Eudesobovatol B	10346031	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3OC4=CC=C(C=C4)CC=C)CC=C)O	504.70	unknown	via CMAUP database
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
Proximadiol	165258	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
(1,2,5-Trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl) but-2-enoate	549549	Click to see CC=CC(=O)OC1CC2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3	332.40	unknown	https://doi.org/10.1021/NP990332L
(10-Hydroxy-1,2,5-trimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl) but-2-enoate	85146315	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CCC(=CC4O2)C)C)C)CO3)O	334.40	unknown	https://doi.org/10.1021/NP990332L
[(1R,2R,7R,10R,11S,12R)-10-hydroxy-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] (Z)-but-2-enoate	163191106	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3)O	348.40	unknown	https://doi.org/10.1021/NP990332L
[(1R,2R,7R,9R,10R,11S,12R)-10-hydroxy-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] (Z)-but-2-enoate	162908969	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3)O	348.40	unknown	https://doi.org/10.1021/NP990332L
[(1S,2R,7R,11R,12S)-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] (Z)-but-2-enoate	9905638	Click to see CC=CC(=O)OC1CC2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3	332.40	unknown	https://doi.org/10.1021/NP990332L
[(1S,2R,7R,9R,10R,11S,12S)-10-hydroxy-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] but-2-enoate	162908970	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3)O	348.40	unknown	https://doi.org/10.1021/NP990332L
[(1S,2R,7R,9R,10R,11S,12S)-10-hydroxy-1,2,5-trimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] but-2-enoate	162916380	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CCC(=CC4O2)C)C)C)CO3)O	334.40	unknown	https://doi.org/10.1021/NP990332L
[(1S,2R,7R,9R,11R,12S)-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] but-2-enoate	162926072	Click to see CC=CC(=O)OC1CC2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3	332.40	unknown	https://doi.org/10.1021/NP990332L
12,13-Epoxy-4-hydroxytrichothec-9-en-8-one crotonate	12444502	Click to see CC=CC(=O)OC1CC2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3	332.40	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
8-Dihydrotrichothecinol A	10449549	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CCC(=CC4O2)C)C)C)CO3)O	334.40	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
Trichothec-9-en-8-one, 12,13-epoxy-4-hydroxy-, (4beta)-	495548	Click to see CC1=CC2C(CC1=O)(C3(C(CC(C34CO4)O2)O)C)C	264.32	unknown	https://doi.org/10.1021/NP990332L
Trichothecinol A	10472929	Click to see CC=CC(=O)OC1C(C2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3)O	348.40	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
Trichothecolon	12444504	Click to see CC1=CC2C(CC1=O)(C3(C(CC(C34CO4)O2)O)C)C	264.32	unknown	https://doi.org/10.1021/NP990332L
Trichothecolone	107974	Click to see CC1=CC2C(CC1=O)(C3(C(CC(C34CO4)O2)O)C)C	264.32	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2R,5R,7R,10S,11R)-5-ethenyl-2,5,11-trimethyl-15-oxatetracyclo[9.3.2.01,10.02,7]hexadecane-8,16-dione	90473942	Click to see CC1(CCC2(C(C1)C(=O)CC3C24CCCC3(C(=O)O4)C)C)C=C	316.40	unknown	https://doi.org/10.1107/S1600536807051215
(1R,2R,5R,7R,9S,10S,11S)-5-ethenyl-9-hydroxy-2,5,11-trimethyl-15-oxatetracyclo[9.3.2.01,10.02,7]hexadecane-8,16-dione	44575189	Click to see CC1(CCC2(C(C1)C(=O)C(C3C24CCCC3(C(=O)O4)C)O)C)C=C	332.40	unknown	https://doi.org/10.1021/NP990332L
(1R,2R,5R,7S,9R,10R,11S)-5-ethenyl-9-hydroxy-2,5,11-trimethyl-15-oxatetracyclo[9.3.2.01,10.02,7]hexadecan-16-one	10358526	Click to see CC1(CCC2(C(C1)CC(C3C24CCCC3(C(=O)O4)C)O)C)C=C	318.40	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
5-Ethenyl-9-hydroxy-2,5,11-trimethyl-15-oxatetracyclo[9.3.2.01,10.02,7]hexadecan-16-one	85120634	Click to see CC1(CCC2(C(C1)CC(C3C24CCCC3(C(=O)O4)C)O)C)C=C	318.40	unknown	https://doi.org/10.1021/NP990332L
5-Ethenyl-9-hydroxy-2,5,11-trimethyl-15-oxatetracyclo[9.3.2.01,10.02,7]hexadecane-8,16-dione	73817326	Click to see CC1(CCC2(C(C1)C(=O)C(C3C24CCCC3(C(=O)O4)C)O)C)C=C	332.40	unknown	https://doi.org/10.1021/NP990332L
6beta-Hydroxyrosenonolactone	21635799	Click to see CC1(CCC2(C(C1)C(=O)C(C3C24CCCC3(C(=O)O4)C)O)C)C=C	332.40	unknown	https://doi.org/10.1021/NP990332L
CID 3081376	3081376	Click to see CC1(CCC2(C(C1)C(=O)CC3C24CCCC3(C(=O)O4)C)C)C=C	316.40	unknown	https://doi.org/10.1021/NP990332L
Rosenonolactone	11723309	Click to see CC1(CCC2(C(C1)C(=O)CC3C24CCCC3(C(=O)O4)C)C)C=C	316.40	unknown	https://doi.org/10.1021/NP990332L
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 2-hydroxy-3-(1-hydroxyoctadecoxy)propanoate	162973870	Click to see CCCCCCCCCCCCCCCCCC(O)OCC(C(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O	783.30	unknown	https://doi.org/10.1021/NP050315Y
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 2-tetracosoxyacetate	73153493	Click to see CCCCCCCCCCCCCCCCCCCCCCCCOCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	821.40	unknown	https://doi.org/10.1021/NP050315Y
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 3-hydroxyicosanoate	75071968	Click to see CCCCCCCCCCCCCCCCCC(CC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O	737.20	unknown	https://doi.org/10.1021/NP050315Y
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (2R)-2-hydroxy-3-[(1R)-1-hydroxyoctadecoxy]propanoate	162973871	Click to see CCCCCCCCCCCCCCCCCC(O)OCC(C(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O	783.30	unknown	https://doi.org/10.1021/NP050315Y
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (3S)-3-hydroxyicosanoate	162874963	Click to see CCCCCCCCCCCCCCCCCC(CC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O	737.20	unknown	https://doi.org/10.1021/NP050315Y
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] 2-hydroxy-3-(1-hydroxynonadecoxy)propanoate	44566237	Click to see CCCCCCCCCCCCCCCCCCC(O)OCC(C(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O	797.30	unknown	https://doi.org/10.1021/NP050315Y
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] 3-hydroxyicosanoate	44566236	Click to see CCCCCCCCCCCCCCCCCC(CC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O	737.20	unknown	https://doi.org/10.1021/NP050315Y
3-O-[2'-(Tetracosyloxy)acetyl]lupeol	11958184	Click to see CCCCCCCCCCCCCCCCCCCCCCCCOCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	821.40	unknown	https://doi.org/10.1021/NP050315Y
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/NP050315Y
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/NP050315Y
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
1-[(3R,8S,9S,10R,13R,14S,17S)-3-amino-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone	162958162	Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)C	315.50	unknown	https://doi.org/10.1055/S-0028-1097412
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
(1S,2R,5S,6S,9R,12S,13S,16R)-N,N,6,7,13-pentamethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine	162847178	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C	356.60	unknown	https://doi.org/10.1055/S-0028-1097412
(1S,2S,5S,6S,9S,12S,13S)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one	162982206	Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C	325.50	unknown	https://doi.org/10.1055/S-0028-1097412
[(1R,2S,5S,6S,9S,10R,12S,13R,16S)-6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-10-yl] 4-methylpent-3-enoate	11178537	Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)NC)C)OC(=O)CC=C(C)C	454.70	unknown	https://doi.org/10.1055/S-0028-1097412
[6,7,13-Trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-10-yl] 4-methylpent-3-enoate	85425809	Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)NC)C)OC(=O)CC=C(C)C	454.70	unknown	https://doi.org/10.1055/S-0028-1097412
6,7,13-Trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one	12310531	Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C	325.50	unknown	https://doi.org/10.1055/S-0028-1097412
Conessine	441082	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C	356.60	unknown	https://doi.org/10.3109/13880209009082835 https://doi.org/10.1016/S0021-9673(01)83481-6 https://doi.org/10.1016/S0031-9422(00)84697-X
Neriine	2860	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C	356.60	unknown	https://doi.org/10.1016/S0021-9673(01)83481-6 https://doi.org/10.1055/S-0028-1097412 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816488/ https://doi.org/10.1080/14786419.2010.537268 https://doi.org/10.3109/13880209009082835 https://doi.org/10.1016/S0031-9422(00)84697-X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685520/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin	9918938	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC3=C2OC(C(O3)C4=CC(=C(C(=C4)OC5=CC=C(C=C5)CC=C)O)O)COC6=C(C=C(C=C6)CC=C)C7=C(C=CC(=C7)CC=C)O)CC=C	827.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol	6093330	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	via CMAUP database
Magnocurarine	53266	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
11-(Hydroxymethyl)-3,6,7-trimethyl-12,13-dioxatetracyclo[8.2.1.01,6.07,11]tridec-2-en-4-one	73209015	Click to see CC1=CC23C(CC1=O)(C4(CCC(C4(O2)CO)O3)C)C	264.32	unknown	https://doi.org/10.1021/NP990332L
13-Acetoxyloukacinol A	10567834	Click to see CC1=CC23C(CC1=O)(C4(C(CC(C4(O2)COC(=O)C)O3)O)C)C	322.40	unknown	https://doi.org/10.1021/NP990332L
8-Hydroxy-11-(hydroxymethyl)-3,6,7-trimethyl-12,13-dioxatetracyclo[8.2.1.01,6.07,11]tridec-2-en-4-one	73208305	Click to see CC1=CC23C(CC1=O)(C4(C(CC(C4(O2)CO)O3)O)C)C	280.32	unknown	https://doi.org/10.1021/NP990332L
Loukacinol A	10516855	Click to see CC1=CC23C(CC1=O)(C4(C(CC(C4(O2)CO)O3)O)C)C	280.32	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
LoukacinolB	10825510	Click to see CC1=CC23C(CC1=O)(C4(CCC(C4(O2)CO)O3)C)C	264.32	unknown	https://doi.org/10.1107/S1600536807051215 https://doi.org/10.1021/NP990332L
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	21629882	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O	624.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan	24796112	Click to see C=CCC1=CC(=C(C=C1)O)C2=C3C(=CC(=C2)CC=C)C=CC(=O)O3	318.40	unknown	via CMAUP database
O-(3-Hydroxy-7-drimen-11-yl)umbelliferone	11898466	Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C	382.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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	via CMAUP database

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Holarrhena floribunda

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