Database	ID/link to page
World Flora Online	wfo-0000495094
Tropicos	50099282
KEW	urn:lsid:ipni.org:names:555079-1
The Plant List	kew-2585422
Open Tree Of Life	7045866
NCBI Taxonomy	2027360
IPNI	555079-1
iNaturalist	542545
GBIF	3745213
EPPO	SHSSP
EOL	5348404
CMAUP	NPO23441

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

α-Glucosidase and Bacterial β-Glucuronidase Inhibitors from the Stems of Schisandra sphaerandra Staph

Rao G, Yu H, Zhang M, Cheng Y, Ran K, Wang J, Wei B, Li M, Shan W, Zhan Z, Ying Y

Pharmaceuticals (Basel)

09-Mar-2022

PMCID:	PMC8954508
doi:	10.3390/ph15030329
PMID:	35337127

Collection calendar: the diversity and local knowledge of wild edible plants used by Chenthang Sherpa people to treat seasonal food shortages in Tibet, China

Ding XY, Zhang Y, Wang L, Zhuang HF, Chen WY, Wang YH

J Ethnobiol Ethnomed

10-Jun-2021

PMCID:	PMC8190990
doi:	10.1186/s13002-021-00464-x
PMID:	34112198

Differentiation in stem and leaf traits among sympatric lianas, scandent shrubs and trees in a subalpine cold temperate forest

Zhang KY, Yang D, Zhang YB, Ellsworth DS, Xu K, Zhang YP, Chen YJ, He F, Zhang JL

Tree Physiol

05-Apr-2021

PMCID:	PMC8597974
doi:	10.1093/treephys/tpab049
PMID:	33823048

Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents

Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A

Sci Total Environ

07-Nov-2020

PMCID:	PMC7833357
doi:	10.1016/j.scitotenv.2020.143539
PMID:	33234268

Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products

Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D

Molecules

29-Apr-2020

PMCID:	PMC7249135
doi:	10.3390/molecules25092070
PMID:	32365518

Detecting Schisandrae Chinensis Fructus and Its Chinese Patent Medicines with a Nucleotide Signature

Jiang W, Ren L, Guo M, Mantri N, Zhao S, Pang X

Genes (Basel)

22-May-2019

PMCID:	PMC6562420
doi:	10.3390/genes10050397
PMID:	31121984

Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus

Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J

Int J Mol Sci

14-May-2018

PMCID:	PMC5983620
doi:	10.3390/ijms19051459
PMID:	29757986

Two New 3,4;9,10-seco-Cycloartane Type Triterpenoids from Illicium difengpi and Their Anti-Inflammatory Activities

Li C, Xi F, Mi J, Wu Z, Chen W

Evid Based Complement Alternat Med

15-May-2013

PMCID:	PMC3671308
doi:	10.1155/2013/942541
PMID:	23762173

Ethnoveterinary plant remedies used by Nu people in NW Yunnan of China

Shen S, Qian J, Ren J

J Ethnobiol Ethnomed

26-Aug-2010

PMCID:	PMC2936877
doi:	10.1186/1746-4269-6-24
PMID:	20796273

Inhibitory effect of essential oils obtained from plants grown in Colombia on yellow fever virus replication in vitro

Meneses R, Ocazionez RE, Martínez JR, Stashenko EE

Ann Clin Microbiol Antimicrob

06-Mar-2009

PMCID:	PMC2661042
doi:	10.1186/1476-0711-8-8
PMID:	19267922

Plant Products as Antimicrobial Agents

Cowan MM

Clin Microbiol Rev

01-Oct-1999

PMCID:	PMC88925
doi:	10.1128/cmr.12.4.564
PMID:	10515903

Nigranoic acid, a triterpenoid from Schisandra sphaerandra that inhibits HIV-1 reverse transcriptase.

Sun HD, Qiu SX, Lin LZ, Wang ZY, Lin ZW, Pengsuparp T, Pezzuto JM, Fong HH, Cordell GA, Farnsworth NR

J Nat Prod

01-May-1996

doi:	10.1021/NP960149H
PMID:	8778243

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)-	9984	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	via CMAUP database
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol	10439806	Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O	714.80	unknown	via CMAUP database
Di-(Z)-feruloylsecoisolariciresinol	24898244	Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O	714.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
triptogelin C-1	10459206	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C	516.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(Z,6R)-6-[(4R,5R,8R,12R,13R)-13-(2-carboxyethyl)-4,8-dimethyl-12-prop-1-en-2-yl-5-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]-2-methylhept-2-enoic acid	5320162	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C	470.70	unknown	https://doi.org/10.1021/NP960149H
11alpha-Methoxyurs-12-ene-3beta,16beta-diol	44235666	Click to see CC1CCC2(C(CC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)OC)C2C1C)C)O)C	472.70	unknown	via CMAUP database
12,23-Dihydroxy-11alpha-methoxyurs-12-ene-3-one	44235900	Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)OC)O)C2C1C)C)C	486.70	unknown	via CMAUP database
13beta,28-Epoxy-23-hydroxyursane-3,12-dione	101485480	Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(=O)C6(C)CO)C)C)C	470.70	unknown	via CMAUP database
13beta,28-Epoxy-3beta-hydroxy-12-oxoursane-23-al	101485479	Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(C6(C)C=O)O)C)C)C	470.70	unknown	via CMAUP database
3beta,12-Dihydroxy-11alpha-methoxyurs-12-ene-23-al	44235896	Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(C5(C)C=O)O)C)C)OC)O)C2C1C)C)C	486.70	unknown	via CMAUP database
6beta,12-Dihydroxy-11alpha-methoxy-24-norurs-12-ene-3-one	44235898	Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CC(C5C4(CCC(=O)C5C)C)O)C)OC)O)C2C1C)C)C	472.70	unknown	via CMAUP database
Microtropioside B	101506966	Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)O)C)C	502.60	unknown	via CMAUP database
Microtropioside C	101506967	Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)OC5C(C(C(C(O5)CO)O)O)O)C)C	664.80	unknown	via CMAUP database
Microtropioside D	101506968	Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(COC5C(C(C(C(O5)CO)O)O)O)O)C)C	664.80	unknown	via CMAUP database
Microtropioside E	101506969	Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C	646.80	unknown	via CMAUP database
Microtropioside F	101506970	Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C	646.80	unknown	via CMAUP database
Nigranoic acid	10814237	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C	470.70	unknown	https://doi.org/10.1021/NP960149H
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
Microtropin A	102448004	Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O	391.40	unknown	via CMAUP database
Microtropin B	102448005	Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O	391.40	unknown	via CMAUP database
Microtropin C	102448006	Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O	391.40	unknown	via CMAUP database
Microtropin D	102448007	Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OCC=C(CO)C#N)O)O)O)O	405.40	unknown	via CMAUP database
Microtropin E	102448008	Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C)O)O)O)O	352.38	unknown	via CMAUP database
Microtropin F	102448009	Click to see CCC(COC1C(C(C(C(O1)COC(=O)C(CC)(C(C)O)O)O)O)O)O	382.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
28-Hydroxy-2,3-secooleana-12-ene 2,3-dioic acid 3-methyl ester	44235899	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)OC)C)C2C1)C)CO)C	502.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	via CMAUP database
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2R,4S,5R,6S,7R,8S,9R,12R)-4,5,12-triacetyloxy-7,8-dibenzoyloxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-6-yl]methyl benzoate	24898243	Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C	756.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,2R,4S,5R,6R,7S,9R,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate	14414924	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C	574.60	unknown	via CMAUP database
15-Acetoxyorbiculin G	24898039	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C6=CC=CC=C6	698.80	unknown	via CMAUP database
1alpha,2alpha-Diacetoxy-6beta,9beta,15-tribenzoyloxy-beta-dihydroagarofuran	16109789	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C	698.80	unknown	via CMAUP database
Mutangin	44419602	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C	636.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Ethyl vanillin	8467	Click to see CCOC1=C(C=CC(=C1)C=O)O	166.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone	75142	Click to see COC1=C(C=CC(=C1)C(=O)CCO)O	196.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Microtropioside A	101506965	Click to see CC1(C2CCC34COCC(C(O3)(CCC4C2(CCC1OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C	500.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
1-Methyl-2-pyrrolidinone	13387	Click to see CN1CCCC1=O	99.13	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin	73571	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B	46229015	Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O	318.32	unknown	via CMAUP database

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Schisandra sphaerandra

Table of Contents

Details Top

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Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

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Distribution (via POWO/KEW) Top

Links to other databases Top