Gnetum montanum

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID644028e10014e666941145
Scientific name	Gnetum montanum
Authority	Markgr.
First published in	Bull. Jard. Bot. Buitenzorg , sér. 3, 10: 466 (1930)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Thoa montana	(Markgr.) Doweld	Turczaninowia 3(4): 33 (2000)

Common names Top

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Language	Common/alternative name
Arabic	جنتوم جبلي
Bulgarian	Планински гнетум
Finnish	vuoriluumio
Chinese	买麻藤
Chinese	湿鼠曲草
Chinese	小籽买麻藤
Chinese	百骑大栗树

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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - Nepal
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000795644
Tropicos	14300201
KEW	urn:lsid:ipni.org:names:383546-1
The Plant List	kew-334171
Open Tree Of Life	673440
NCBI Taxonomy	3381
IUCN Red List	194926
IPNI	383546-1
iNaturalist	135917
GBIF	2653221
EOL	1113977
USDA GRIN	420081

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_015680685.1	Gmon01	Scaffold	Novogene	2020-11-24	302.0x	2.00 Gb

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

Origin, evolution, and diversification of inositol 1,4,5-trisphosphate 3-kinases in plants and animals

Xiong T, Zhang Z, Fan T, Ye F, Ye Z

BMC Genomics

08-Apr-2024

PMCID:	PMC11000326
doi:	10.1186/s12864-024-10257-7
PMID:	38589807

Genomic evidence for rediploidization and adaptive evolution following the whole-genome triplication

Feng X, Chen Q, Wu W, Wang J, Li G, Xu S, Shao S, Liu M, Zhong C, Wu CI, Shi S, He Z

Nat Commun

22-Feb-2024

PMCID:	PMC10884412
doi:	10.1038/s41467-024-46080-7
PMID:	38388712

Callose in leptoid cell walls of the moss Polytrichum and the evolution of callose synthase across bryophytes

Renzaglia K, Duran E, Sagwan-Barkdoll L, Henry J

Front Plant Sci

07-Feb-2024

PMCID:	PMC10879339
doi:	10.3389/fpls.2024.1357324
PMID:	38384754

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

Unraveling the evolutionary dynamics of the TPS gene family in land plants

Yan XM, Zhou SS, Liu H, Zhao SW, Tian XC, Shi TL, Bao YT, Li ZC, Jia KH, Nie S, Guo JF, Kong L, Porth IM, Mao JF

Front Plant Sci

12-Oct-2023

PMCID:	PMC10600500
doi:	10.3389/fpls.2023.1273648
PMID:	37900760

PlantCHRs: A comprehensive database of plant chromatin remodeling factors

Yan H, Liu F, Zhang G, Liu S, Ma W, Yang T, Li Y, Yang J, Cui H

Comput Struct Biotechnol J

05-Oct-2023

PMCID:	PMC10589754
doi:	10.1016/j.csbj.2023.10.005
PMID:	37867975

Genome and whole-genome resequencing of Cinnamomum camphora elucidate its dominance in subtropical urban landscapes

Li D, Lin HY, Wang X, Bi B, Gao Y, Shao L, Zhang R, Liang Y, Xia Y, Zhao YP, Zhou X, Zhang L

BMC Biol

12-Sep-2023

PMCID:	PMC10496300
doi:	10.1186/s12915-023-01692-1
PMID:	37697363

Bioinformatics Analysis of MSH1 Genes of Green Plants: Multiple Parallel Length Expansions, Intron Gains and Losses, Partial Gene Duplications, and Alternative Splicing

Bai MZ, Guo YY

Int J Mol Sci

03-Sep-2023

PMCID:	PMC10487979
doi:	10.3390/ijms241713620
PMID:	37686425

The genome of the Wollemi pine, a critically endangered “living fossil” unchanged since the Cretaceous, reveals extensive ancient transposon activity

Stevenson DW, Ramakrishnan S, de Santis Alves C, Coelho LA, Kramer M, Goodwin S, Ramos OM, Eshel G, Sondervan VM, Frangos S, Zumajo-Cardona C, Jenike K, Ou S, Wang X, Lee YP, Loke S, Rossetto M, McPherson H, Nigris S, Moschin S, Little DP, Katari MS, Varala K, Kolokotronis SO, Ambrose B, Croft LJ, Coruzzi GM, Schatz M, McCombie WR, Martienssen RA

bioRxiv

24-Aug-2023

PMCID:	PMC10473749
doi:	10.1101/2023.08.24.554647
PMID:	37662366

Genome-Wide Comparison and Functional Characterization of HMGR Gene Family Associated with Shikonin Biosynthesis in Lithospermum erythrorhizon

Wang X, Wang C, Yang M, Jie W, Fazal A, Fu J, Yin T, Cai J, Liu B, Lu G, Lin H, Han H, Wen Z, Qi J, Yang Y

Int J Mol Sci

07-Aug-2023

PMCID:	PMC10419935
doi:	10.3390/ijms241512532
PMID:	37569907

Lost in the bloom: DNA-PKcs in green plants

Kumar KR

Front Plant Sci

28-Jul-2023

PMCID:	PMC10419180
doi:	10.3389/fpls.2023.1231678
PMID:	37575944

Evolution of cytosolic and organellar invertases empowered the colonization and thriving of land plants

Wan H, Zhang Y, Wu L, Zhou G, Pan L, Fernie AR, Ruan YL

Plant Physiol

11-Jul-2023

PMCID:	PMC10661998
doi:	10.1093/plphys/kiad401
PMID:	37429000

Analysis of polycomb repressive complex 2 (PRC2) subunits in Picea abies with a focus on embryo development

Zhu T, Hu J, Yang X, Kong L, Ling J, Wang J, An S

BMC Plant Biol

01-Jul-2023

PMCID:	PMC10314529
doi:	10.1186/s12870-023-04359-9
PMID:	37391710

Quartet Fiduccia–Mattheyses revisited for larger phylogenetic studies

Mim SA, Zarif-Ul-Alam M, Reaz R, Bayzid MS, Rahman MS

Bioinformatics

07-Jun-2023

PMCID:	PMC10260390
doi:	10.1093/bioinformatics/btad332
PMID:	37285316

Genome-wide identification and expression profiling of B3 transcription factor genes in Populus alba × Populus glandulosa

Wei M, Li H, Wang Q, Liu R, Yang L, Li Q

Front Plant Sci

30-May-2023

PMCID:	PMC10262750
doi:	10.3389/fpls.2023.1193065
PMID:	37324718

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Aporphines
15-Methoxy-10,10-dimethyl-10-azoniatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaene-4,5,16-triol	56833653	Click to see C[N+]1(CCC2=CC(=C(C3=C4C=C(C(=CC4=CC1=C23)O)O)O)OC)C	326.40	unknown	https://doi.org/10.1021/NP200700F
2-methoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1,9,10-triol	57394259	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)O)O)OC)C	328.40	unknown	https://doi.org/10.1021/NP200700F
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine	5610	Click to see C1=CC(=CC=C1CCN)O	137.18	unknown	https://doi.org/10.1021/NP200700F
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
4-Hydroxyphenylacetaldehyde	440113	Click to see C1=CC(=CC=C1CC=O)O	136.15	unknown	https://doi.org/10.1021/NP200700F
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
4-Hydroxyphenylpyruvic acid	979	Click to see C1=CC(=CC=C1CC(=O)C(=O)O)O	180.16	unknown	https://doi.org/10.1021/NP200700F
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
Dopamine	681	Click to see C1=CC(=C(C=C1CCN)O)O	153.18	unknown	https://doi.org/10.1021/NP200700F
> Benzenoids / Phenols / Benzenediols / Resorcinols
GnetifolinC	145709262	Click to see CC1=C(C2=C(C3=C(C=C(C=C3)O)C(C(C4=C1C=CC(=C4)O)C5=CC(=CC(=C5)O)O)OC)C(=CC(=C2)O)O)OC	528.50	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
> Lignans, neolignans and related compounds
1-(4-Hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propane-1,3-diol	193323	Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O	376.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
1,3-Propanediol, 1-(4-hydroxy-3-methoxyphenyl)-2-[4-[(1E)-3-hydroxy-1-propen-1-yl]-2-methoxyphenoxy]-, (1S,2S)-	101928611	Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O	376.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol (6CI); (+)-Cyclolariciresinol; (+)-Isolariciresinol; Isolariciresinol, (+)-;-Conidendryl alcohol	4177125	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
> Lignans, neolignans and related compounds / Furanoid lignans
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol	4546425	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	234817	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Medioresinol	181681	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Syringaresinol	100067	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol	332427	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol	134203	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Isolariciresinol 9'-O-glucoside	93473218	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1007/S10600-009-9325-Y
(2S,3R,4S,5S,6R)-2-[4-[(1R,2R)-1,3-dihydroxy-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]propyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163194388	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(C(CO)OC3=C(C=C(C=C3)C=CCO)OC)O	568.60	unknown	https://doi.org/10.1007/S10600-009-9325-Y
2-[[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	24150655	Click to see COC1=C(C=CC(=C1)CC2COC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Isolariciresinol 9'-O-beta-D-glucoside	74191750	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1007/S10600-009-9325-Y
Lariciresinol 9-O-\|A-D-glucopyranoside	145709428	Click to see COC1=C(C=CC(=C1)CC2COC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1007/S10600-009-9325-Y
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
[(3aR,5R,5aS,6R,7R,8R,8aS,9aR)-6,7-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,7-b]furan-8-yl] acetate	163032763	Click to see CC1CC2C(CC3(C1C(C(C3OC(=O)C)O)O)C)C(=C)C(=O)O2	324.40	unknown	https://doi.org/10.1007/S10600-009-9325-Y
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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	https://doi.org/10.1016/S0367-326X(01)00370-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1016/S0367-326X(01)00370-7
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	https://doi.org/10.1016/S0367-326X(01)00370-7
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-6-Methoxy-1-((4-methoxyphenyl)methyl)-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol	177088	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)O)OC	313.40	unknown	https://doi.org/10.1021/NP200700F
(S)-N-Methylcoclaurine	440584	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC	299.40	unknown	https://doi.org/10.1021/NP200700F
(S)-Norcoclaurine	440927	Click to see C1CNC(C2=CC(=C(C=C21)O)O)CC3=CC=C(C=C3)O	271.31	unknown	https://doi.org/10.1021/NP200700F
1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol	5319197	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	https://doi.org/10.1021/NP200700F
Coclaurine	160487	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	https://doi.org/10.1021/NP200700F
Magnocurarine	53266	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	https://doi.org/10.1021/NP200700F
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(9R,17R)-1-azoniahexacyclo[15.8.0.01,9.02,7.011,16.018,23]pentacosa-2,4,6,11(16),12,14,18,20,22-nonaene-4,5,12,13,20,21-hexol	57399480	Click to see C1C[N+]23C(CC4=CC(=C(C=C42)O)O)CC5=C(C3C6=CC(=C(C=C61)O)O)C=CC(=C5O)O	420.40	unknown	https://doi.org/10.1021/NP200700F
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(3-Hydroxy-5-methoxyphenyl)-1-benzofuran-4-ol	641364	Click to see COC1=CC(=CC(=C1)O)C2=CC3=C(C=CC=C3O2)O	256.25	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7 https://doi.org/10.1002/HLCA.200890007
Epsilon-viniferin	5281728	Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O	454.50	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
Gnetofuran B	11108903	Click to see COC1=CC(=CC(=C1)O)C2=CC3=C(O2)C=CC(=C3OC)O	286.28	unknown	https://doi.org/10.1002/HLCA.200890007
Gnetumelin B	101839192	Click to see COC1=CC(=C(C=C1C2=CC3=C(O2)C=CC(=C3OC)O)O)OC	316.30	unknown	https://doi.org/10.1002/HLCA.200890007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-	5056	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	https://doi.org/10.1002/HLCA.200890007 https://doi.org/10.1016/S0367-326X(01)00370-7
2-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,3-diol	53395260	Click to see C1=CC(=C(C(=C1)O)C=CC2=CC(=CC(=C2)O)O)O	244.24	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
4-Benzyl-5-[2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol	138112828	Click to see C1=CC=C(C=C1)CC2=C(C=C(C=C2O)O)C=CC3=CC(=C(C=C3)O)O	334.40	unknown	https://doi.org/10.1002/HLCA.200890007
5-[(2R,3R)-3-(3-hydroxy-4-methoxyphenyl)oxiran-2-yl]benzene-1,2,3-triol	163031572	Click to see COC1=C(C=C(C=C1)C2C(O2)C3=CC(=C(C(=C3)O)O)O)O	290.27	unknown	https://doi.org/10.1002/HLCA.200890007
5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]benzene-1,3-diol	53394021	Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O	258.27	unknown	https://doi.org/10.1002/HLCA.200890007
5-[(Z)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]benzene-1,3-diol	10879760	Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O	258.27	unknown	https://doi.org/10.1002/HLCA.200890007
5-[3-(3-Hydroxy-4-methoxyphenyl)oxiran-2-yl]benzene-1,2,3-triol	163031571	Click to see COC1=C(C=C(C=C1)C2C(O2)C3=CC(=C(C(=C3)O)O)O)O	290.27	unknown	https://doi.org/10.1002/HLCA.200890007
CID 73197	73197	Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O	244.24	unknown	https://doi.org/10.1002/HLCA.200890007
Gnetol	45382232	Click to see C1=CC(=C(C(=C1)O)C=CC2=CC(=CC(=C2)O)O)O	244.24	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
Gnetumelin A	101839191	Click to see C1=CC=C(C=C1)CC2=C(C=C(C=C2O)O)C=CC3=CC(=C(C=C3)O)O	334.40	unknown	https://doi.org/10.1002/HLCA.200890007
Isorhapontigenin	5318650	Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O	258.27	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
Oxyresveratrol	5281717	Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O	244.24	unknown	https://doi.org/10.1002/HLCA.200890007
Resveratrol	445154	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7 https://doi.org/10.1002/HLCA.200890007
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
2-[3-Hydroxy-5-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5090283	Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	420.40	unknown	https://doi.org/10.1002/HLCA.200890007
Gnetifolin E	13783629	Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O	420.40	unknown	https://doi.org/10.1016/S0367-326X(01)00370-7
Isorhapontin	5281716	Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	420.40	unknown	https://doi.org/10.1002/HLCA.200890007

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Gnetum montanum

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