Scientific name	Authority	First published in
Psiadia dodonaeifolia	Steetz	Naturw. Reise Mossambique 6(Bot., 2): 385 (1864)
Psiadia arabica	Jaub. & Spach	Ill. Pl. Orient. 4(36): 85. tt. 352, 353 (1852)
Psiadia aparine	Muschl.	Bot. Jahrb. Syst. 46(1-2): 103 (1911)
Nidorella punctulata	DC.	Prodr. 5: 323 (1836)
Psiadia vernicosa	Schinz	Bull. Herb. Boissier vi. 559 (non Steetz).
Baccharis resiniflua	Steud. & Hochst. ex DC.	Prodr. 7(1): 282 (1838)
Psiadia resiniflora	Sch.Bip. ex Schweinf.	Beitr. Fl. Aethiop. : 286 (1867)
Psiadia resiniflua	(Hochst. & Steud. ex DC.) Sch.Bip.	Beitr. Fl. Aethiop. 308

Common names Top

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Language	Common/alternative name
Arabic	شوزم منقط

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
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- Northern Africa
  - Libya
- South Tropical Africa
  - Angola
  - Mozambique
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Namibia
  - Northern Provinces

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
  - Saudi Arabia
  - Yemen

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000047536
Tropicos	50076058
KEW	urn:lsid:ipni.org:names:239938-1
The Plant List	gcc-146006
Open Tree Of Life	532481
NCBI Taxonomy	72969
IPNI	239938-1
iNaturalist	199960
GBIF	3119760
CMAUP	NPO7047

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

Ethnobotanical study on medicinal plants in Melit area (North Darfur), Western Sudan

Muhakr MA, Ahmed IM, El hassan GO, Yagi S

J Ethnobiol Ethnomed

03-Jan-2024

PMCID:	PMC10765873
doi:	10.1186/s13002-023-00646-9
PMID:	38172804

Medicinal Plants Used in the Management of Sexual Dysfunction, Infertility and Improving Virility in the East African Community: A Systematic Review

Kyarimpa C, Nagawa CB, Omara T, Odongo S, Ssebugere P, Lugasi SO, Gumula I

Evid Based Complement Alternat Med

12-Aug-2023

PMCID:	PMC10439835
doi:	10.1155/2023/6878852
PMID:	37600549

Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches

Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF

Plants (Basel)

02-Mar-2023

PMCID:	PMC10005506
doi:	10.3390/plants12051145
PMID:	36904005

Flavonoids as a therapeutical option for the treatment of thrombotic complications associated with COVID‐19

Quintal Martínez JP, Segura Campos MR

Phytother Res

08-Dec-2022

PMCID:	PMC9878134
doi:	10.1002/ptr.7700
PMID:	36480428

Saudi Arabian Plants: A Powerful Weapon against a Plethora of Diseases

El-Seedi HR, Kotb SM, Musharraf SG, Shehata AA, Guo Z, Alsharif SM, Saeed A, Hamdi OA, Tahir HE, Alnefaie R, Verpoorte R, Khalifa SA

Plants (Basel)

08-Dec-2022

PMCID:	PMC9783889
doi:	10.3390/plants11243436
PMID:	36559548

Bio-Guided Isolation of SARS-CoV-2 Main Protease Inhibitors from Medicinal Plants: In Vitro Assay and Molecular Dynamics

Abdallah HM, El-Halawany AM, Darwish KM, Algandaby MM, Mohamed GA, Ibrahim SR, Koshak AE, Elhady SS, Fadil SA, Alqarni AA, Abdel-Naim AB, Elfaky MA

Plants (Basel)

24-Jul-2022

PMCID:	PMC9332707
doi:	10.3390/plants11151914
PMID:	35893619

Diterpenoid Constituents of Psiadiapunctulata and Evaluation of Their Antimicrobial Activity

Donadio G, Chini MG, Parisi V, Mensitieri F, Malafronte N, Bifulco G, Bisio A, De Tommasi N, Bader A

J Nat Prod

24-Jun-2022

PMCID:	PMC9315948
doi:	10.1021/acs.jnatprod.1c01093
PMID:	35748331

Molecular Structure-Based Screening of the Constituents of Calotropis procera Identifies Potential Inhibitors of Diabetes Mellitus Target Alpha Glucosidase

Adinortey CA, Kwarko GB, Koranteng R, Boison D, Obuaba I, Wilson MD, Kwofie SK

Curr Issues Mol Biol

21-Feb-2022

PMCID:	PMC8928985
doi:	10.3390/cimb44020064
PMID:	35723349

Umuhengerin Neuroprotective Effects in Streptozotocin-Induced Alzheimer’s Disease Mouse Model via Targeting Nrf2 and NF-Kβ Signaling Cascades

Sirwi A, El Sayed NS, Abdallah HM, Ibrahim SR, Mohamed GA, El-Halawany AM, Safo MK, Abdel Rasheed NO

Antioxidants (Basel)

18-Dec-2021

PMCID:	PMC8698785
doi:	10.3390/antiox10122011
PMID:	34943114

Impacts of Nicotiana glauca Graham Invasion on the Vegetation Composition and Soil: A Case Study of Taif, Western Saudi Arabia

Assaeed AM, Alharthi AS, Abd-ElGawad AM

Plants (Basel)

25-Nov-2021

PMCID:	PMC8708854
doi:	10.3390/plants10122587
PMID:	34961058

GC-MS- and NMR-Based Metabolomics and Molecular Docking Reveal the Potential Alpha-Glucosidase Inhibitors from Psychotria malayana Jack Leaves

Nipun TS, Khatib A, Ibrahim Z, Ahmed QU, Redzwan IE, Primaharinastiti R, Saiman MZ, Fairuza R, Widyaningsih TD, AlAjmi MF, Khalifa SA, El-Seedi HR

Pharmaceuticals (Basel)

26-Sep-2021

PMCID:	PMC8541227
doi:	10.3390/ph14100978
PMID:	34681203

Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature

Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F

Malar J

25-Aug-2021

PMCID:	PMC8390284
doi:	10.1186/s12936-021-03866-0
PMID:	34433465

Phytomedicine from Middle Eastern Countries: An Alternative Remedy to Modern Medicine against Candida spp Infection

Alam MZ, Ahmad Khan MS

Evid Based Complement Alternat Med

14-Jul-2021

PMCID:	PMC8298167
doi:	10.1155/2021/6694876
PMID:	34335836

Self-Nanoemulsifying Drug Delivery System Loaded with Psiadia punctulata Major Metabolites for Hypertensive Emergencies: Effect on Hemodynamics and Cardiac Conductance

Abdallah HM, El-Bassossy HM, El-Halawany AM, Ahmed TA, Mohamed GA, Malebari AM, Hassan NA

Front Pharmacol

10-Jun-2021

PMCID:	PMC8222910
doi:	10.3389/fphar.2021.681070
PMID:	34177590

Natural plant species inventory of hotspot areas in Arabian Peninsula: Southwest Al-Baha region, Saudi Arabia

Al-Namazi AA, Al-Khulaidi AW, Algarni S, Al-Sagheer NA

Saudi J Biol Sci

04-Mar-2021

PMCID:	PMC8176062
doi:	10.1016/j.sjbs.2021.02.076
PMID:	34121869

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
4-[(2-amino-4-oxo-1H-pteridin-6-yl)methyl-formylamino]benzoic acid	97575	Click to see C1=CC(=CC=C1C(=O)O)N(CC2=CN=C3C(=N2)C(=O)N=C(N3)N)C=O	340.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,3S,4R,9R,10S,13S)-3-hydroxy-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-one	162846821	Click to see CC12CC(=O)CC(C1C(CC34C2CCC(C3)C(=C)C4)O)(CO)CO	334.40	unknown	https://doi.org/10.1016/0031-9422(93)80032-N
(1R,4R,7R,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-ol	162920705	Click to see CC12CC(CC(C1CCC34C2CCC(C3)C(=C)C4)(CO)CO)O	320.50	unknown	https://doi.org/10.1016/0031-9422(93)80032-N
(1R,4R,7S,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-ol	11897962	Click to see CC12CC(CC(C1CCC34C2CCC(C3)C(=C)C4)(CO)CO)O	320.50	unknown	https://doi.org/10.1016/0031-9422(93)80032-N
(1R,4R,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-one	163034477	Click to see CC12CC(=O)CC(C1CCC34C2CCC(C3)C(=C)C4)(CO)CO	318.40	unknown	https://doi.org/10.1016/0031-9422(93)80032-N
(1S,3R,4S,7R,9S,10R,12R,13R,14S)-5,5-bis(hydroxymethyl)-9,13-dimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-3,7-diol	162899099	Click to see CC12CC(CC(C1C(CC34C2CC5C(C3)C5(C4)C)O)(CO)CO)O	336.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.007
(1S,4S,7S,9S,10R,12R,13R,14S)-5,5-bis(hydroxymethyl)-9,13-dimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecan-7-ol	95118006	Click to see CC12CC(CC(C1CCC34C2CC5C(C3)C5(C4)C)(CO)CO)O	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.007
(1S,4S,9S,10R,13R)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-one	101630422	Click to see CC12CC(=O)CC(C1CCC34C2CCC(C3)C(=C)C4)(CO)CO	318.40	unknown	https://doi.org/10.1016/0031-9422(92)83648-I https://doi.org/10.1016/0031-9422(93)80032-N https://doi.org/10.1016/S0031-9422(96)00812-6
14-Hydroxy-14-(hydroxymethyl)-5,5-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-9-carboxylic acid	24121270	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C(=O)O)C	336.50	unknown	https://doi.org/10.1016/S0031-9422(96)00812-6
2-Hydroxy-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid	73028428	Click to see CC12CCCC(C1CC(C34C2CC5C(C3)C5(C4)C)O)(C)C(=O)O	318.40	unknown	https://doi.org/10.1016/S0031-9422(96)00812-6
3-Hydroxy-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-one	162846820	Click to see CC12CC(=O)CC(C1C(CC34C2CCC(C3)C(=C)C4)O)(CO)CO	334.40	unknown	https://doi.org/10.1016/0031-9422(93)80032-N
5,5-Bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-ol	53396113	Click to see CC12CC(CC(C1CCC34C2CCC(C3)C(=C)C4)(CO)CO)O	320.50	unknown	https://doi.org/10.1016/0031-9422(93)80032-N https://doi.org/10.1016/S0031-9422(96)00812-6
5,5-Bis(hydroxymethyl)-9,13-dimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecan-7-ol	23844025	Click to see CC12CC(CC(C1CCC34C2CC5C(C3)C5(C4)C)(CO)CO)O	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.007
5,5-Bis(hydroxymethyl)-9,13-dimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-3,7-diol	5056918	Click to see CC12CC(CC(C1C(CC34C2CC5C(C3)C5(C4)C)O)(CO)CO)O	336.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.007
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid	5280896	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	92835934	Click to see CC12CCCCC1C(CC3C2C(CC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(3beta,5alpha,7alpha)-3,7-Dihydroxyandrostan-17-one	9815044	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3R,5R,7S,8R,9S,10S,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	57386710	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3R,5R,8R,9S,10S,13S,14S,17S)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	69924431	Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3R,5R,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-7,17-dione	57386713	Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
(3R,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	69766330	Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3S,5R,7R,8S,9S,10S,13R,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,16-triol	99574281	Click to see CC12CCC3C(C1CC(C2)O)C(CC4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
(3S,5R,7S,8S,9S,10S,13S,14S,16S)-3,7,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99572894	Click to see CC12CCC(CC1CC(C3C2C(=O)CC4(C3CC(C4)O)C)O)O	322.40	unknown	via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	99573267	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	99573266	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,6S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol	99574278	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	99571962	Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	99571961	Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99601533	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99575783	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
(5R,8S,9S,10S,13R,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-dione	99571971	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(=O)C4)C	304.40	unknown	via CMAUP database
(5S,6R,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573707	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16R)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573706	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573705	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99574441	Click to see CC12CCCC1C3CC(C4CC(=O)CCC4(C3C(C2)O)C)O	306.40	unknown	via CMAUP database
(5S,8S,9R,10S,13S,14S,16R)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione	99571360	Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O	320.40	unknown	via CMAUP database
(5S,8S,9R,10S,13S,14S,16S)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione	99571358	Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O	320.40	unknown	via CMAUP database
(5S,8S,9S,10S,13S,14S,16R)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	99574177	Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C	304.40	unknown	via CMAUP database
(5S,8S,9S,10S,13S,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	99574175	Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C	304.40	unknown	via CMAUP database
11-Hydroxyandrosterone	21139727	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
11alpha-Hydroxy-5alpha-androstane-3,17-dione	101709630	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
11alpha,16alpha-Dihydroxy-5alpha-androstan-3-one	100922644	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
3beta-Hydroxy-5alpha-androstane-7,17-dione	11954160	Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
3beta,6alpha,17beta-Trihydroxy-5alpha-androstane	170796	Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
5,17beta-Dihydroxy-5alpha-androstane-3-one	10979706	Click to see CC12CCC3C(C1CCC2O)CCC4(C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-11-one, 3alpha,17beta-dihydroxy-	10125601	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CCC4O)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-3-one, 11alpha,17beta-dihydroxy-	22796602	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4O)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-3beta,17beta-diol-7-one	11868973	Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
5alpha-Androstan-6-one, 3beta,17beta-dihydroxy-	11551286	Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
5alpha-Androstane-3,7,17-trione	11266632	Click to see CC12CCC(=O)CC1CC(=O)C3C2CCC4(C3CCC4=O)C	302.40	unknown	via CMAUP database
5alpha-Androstane-3beta,11alpha,16beta-triol	100922640	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CC(C4)O)C)O)O	308.50	unknown	via CMAUP database
5alpha-Androstane-3beta,11alpha,17beta-triol	57396177	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4O)C)O)O	308.50	unknown	via CMAUP database
6alpha-Hydroxy-EPIA	15917986	Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
7-beta-Hydroxyepiandrosterone	9836181	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
Androstan-3-one, 6,17-dihydroxy-, (5alpha,6alpha,17beta)-	15838416	Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
Androstan-6-one, 3,17-dihydroxy-, (3alpha,5alpha,17beta)-	15929496	Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
Androstane-3,17-dione, 6-hydroxy-, (5alpha,6alpha)-	22296022	Click to see CC12CCC(=O)CC1C(CC3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
Jgd4N79M5A	68995028	Click to see CC12CCC3C(C1CCC2O)C(CC4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
10-Hydroxy-3-oxoestr-4-en-17-yl acetate	91691749	Click to see CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34O)C	332.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
Butanedioate;hydron	21952380	Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-]	118.09	unknown	via CMAUP database
Glutaric acid	743	Click to see C(CC(=O)O)CC(=O)O	132.11	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate	3698251	Click to see C(C(=O)[O-])[OH2+]	76.05	unknown	via CMAUP database
> Organoheterocyclic compounds / Azolidines / Isoxazolidines / Phenylisoxazolidines
Asperidine C	145985497	Click to see CCCCCCCCCC1CC(C2CN1OC2C3=CC=CC=C3)O	331.50	unknown	https://doi.org/10.1016/0031-9422(93)80032-N https://doi.org/10.1016/S0031-9422(96)00812-6 https://doi.org/10.1016/0031-9422(92)83648-I
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
Quininic acid	345824	Click to see COC1=CC2=C(C=CN=C2C=C1)C(=O)O	203.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(E)-3-(4-Hydroxyphenyl)acrylic acid docosylester	10005036	Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	472.70	unknown	https://doi.org/10.1016/S0031-9422(01)00147-9
(Z)-3-(4-Hydroxyphenyl)acrylic acid docosylester	12083115	Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	472.70	unknown	https://doi.org/10.1016/S0031-9422(01)00147-9
4-Hydroxy-trans-cinnamic acid icosyl ester	15139446	Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	444.70	unknown	https://doi.org/10.1271/BBB.61.2127
Docosyl 3-(4-hydroxyphenyl)prop-2-enoate	53396120	Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	472.70	unknown	https://doi.org/10.1016/S0031-9422(01)00147-9
icosyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate	102094141	Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	444.70	unknown	https://doi.org/10.1271/BBB.61.2127
Icosyl 3-(4-hydroxyphenyl)prop-2-enoate	54130386	Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	444.70	unknown	https://doi.org/10.1271/BBB.61.2127
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
5,7,4'-Trihydroxy-2',3',5'-trimethoxyflavone	5323559	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC)OC)O	360.30	unknown	https://doi.org/10.1016/S0031-9422(01)00147-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-2',3',4',5'-tetramethoxyflavone	5742694	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC)OC)OC	374.30	unknown	https://doi.org/10.1016/S0031-9422(01)00147-9
5,7,3'-Trihydroxy-2',4',5'-trimethoxyflavone	7330522	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC)O)OC	360.30	unknown	https://doi.org/10.1016/0031-9422(92)83648-I https://doi.org/10.1016/S0031-9422(01)00147-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxy-2,3,5-trimethoxyphenyl)-7-methoxychromen-4-one	7330523	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3OC)OC)O)OC)O	374.30	unknown	https://doi.org/10.1016/S0031-9422(01)00147-9
5-Hydroxy-7-methoxy-2-(2,3,4,5-tetramethoxyphenyl)chromen-4-one	5742693	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3OC)OC)OC)OC)O	388.40	unknown	https://doi.org/10.1016/0031-9422(90)80222-3 https://doi.org/10.1016/S0031-9422(01)00147-9
5,3'-Dihydroxy-7,2',4',5'-tetramethoxyflavone	14704513	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3OC)O)OC)OC)O	374.30	unknown	https://doi.org/10.1016/0031-9422(90)80222-3
Psiadiarabicin	14704514	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O)OC	404.40	unknown	https://doi.org/10.1016/S0031-9422(00)83901-1 https://doi.org/10.1016/0031-9422(90)80222-3

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Psiadia punctulata

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