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Peganum nigellastrum

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64404fdc6d276060508894
Scientific name Peganum nigellastrum
Authority Bunge
First published in Enum. Pl. China Bor. : 13 (1833)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Persian پگانوم نیگلاستروم
Russian Гармала чернушкообразная
Chinese 驼驼蒿
Chinese 骆驼蒿
Chinese 骆驼蓬子
Chinese 匐根骆驼蓬

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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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
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Xinjiang
    • Mongolia
      • Mongolia
    • Siberia
      • Buryatiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001146400
Tropicos 34600193
KEW urn:lsid:ipni.org:names:774547-1
The Plant List tro-34600193
Open Tree Of Life 1056016
Observations.org 135626
NCBI Taxonomy 673036
IPNI 774547-1
iNaturalist 852388
GBIF 3986712
Freebase /m/010lrhx8
EOL 2888499
Elurikkus 446669
USDA GRIN 408768
Wikipedia Peganum_nigellastrum

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
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
The complete chloroplast genome sequence of Zygophyllum kansuense Y. X. Liou (Zygophyllaceae) Wang N, Wang S, Zhang L, Chang ZY Mitochondrial DNA B Resour 27-Oct-2022
PMCID:PMC9621224
doi:10.1080/23802359.2022.2135396
PMID:36325281
The Endophytic Fungi Diversity, Community Structure, and Ecological Function Prediction of Sophora alopecuroides in Ningxia, China Wang R, Zhang Q, Ju M, Yan S, Zhang Q, Gu P Microorganisms 22-Oct-2022
PMCID:PMC9695620
doi:10.3390/microorganisms10112099
PMID:36363690
Recent advances and prospects in the organocatalytic synthesis of quinazolinones Borah B, Swain S, Patat M, Chowhan LR Front Chem 14-Sep-2022
PMCID:PMC9515322
doi:10.3389/fchem.2022.991026
PMID:36186594
Facile One-Pot Synthesis of Functionalized Quinoline-Fused Fluorescent Dihydro/Spiro-quinazolinone Derivatives George K, Elavarasan P, Ponnusamy S, Sathananthan K ACS Omega 09-Jun-2022
PMCID:PMC9219092
doi:10.1021/acsomega.2c00674
PMID:35755376
Sunflower-Assisted Bio-Derived ZnO-NPs as an Efficient Nanocatalyst for the Synthesis of Novel Quinazolines with Highly Antioxidant Activities S. M, Narasaiah BP, B. H, G. L. B, Pradeepkiran JA, Padhy H Antioxidants (Basel) 31-Mar-2022
PMCID:PMC9025409
doi:10.3390/antiox11040688
PMID:35453373
Toward the Allelopathy of Peganum sp. and Related Chemical Constituents in Agriculture Bitchagno GT, El Bouhssini M, Mahdi I, Ward JL, Sobeh M Front Plant Sci 21-Jan-2022
PMCID:PMC8813868
doi:10.3389/fpls.2021.796103
PMID:35126420
Comparative Chloroplast Genomics and Phylogenetic Analysis of Zygophyllum (Zygophyllaceae) of China Zhang L, Wang S, Su C, Harris A, Zhao L, Su N, Wang JR, Duan L, Chang ZY Front Plant Sci 24-Sep-2021
PMCID:PMC8500179
doi:10.3389/fpls.2021.723622
PMID:34630471
The complete chloroplast genome sequence of medicinal plant: Peganum nigellastrum (Zygophyllaceae) Zhang L, Wang Z, Chang L, Wei Y Mitochondrial DNA B Resour 19-Jul-2021
PMCID:PMC8291069
doi:10.1080/23802359.2021.1950061
PMID:34350349
Peganum spp.: A Comprehensive Review on Bioactivities and Health-Enhancing Effects and Their Potential for the Formulation of Functional Foods and Pharmaceutical Drugs Sharifi-Rad J, Quispe C, Herrera-Bravo J, Semwal P, Painuli S, Özçelik B, Hacıhasanoğlu FE, Shaheen S, Sen S, Acharya K, Amirian M, Castillo CM, López MD, Schoebitz M, Martorell M, Goloshvili T, Al-Harrasi A, Al-Rawahi A, Kumar M, Suleria HA, Cho WC Oxid Med Cell Longev 27-Jun-2021
PMCID:PMC8260309
doi:10.1155/2021/5900422
PMID:34257813
Morphological structures and histochemistry of roots and shoots in Myricaria laxiflora (Tamaricaceae) Li L, Wu D, Zhen Q, Zhang J, Qiu L, Huang G, Yang C Open Life Sci 10-May-2021
PMCID:PMC8114956
doi:10.1515/biol-2021-0049
PMID:34017920
Design and Synthesis of C-Aryl Angular Luotonins via One-Pot Aza-Nazarov–Friedlander Sequence and Their Topo-I Inhibition Studies Along with C-Aryl Vasicinones and Luotonins Rasapalli S, Sammeta VR, Murphy ZF, Golen JA, Agama K, Pommier Y, Savinov SN Bioorg Med Chem Lett 30-Mar-2021
PMCID:PMC8113096
doi:10.1016/j.bmcl.2021.127998
PMID:33794318
Molecularly Imprinted Polymer (MIP) Applications in Natural Product Studies Based on Medicinal Plant and Secondary Metabolite Analysis Karimi Baker Z, Sardari S Iran Biomed J 10-Jan-2021
PMCID:PMC7921521
doi:10.29252/ibj.25.2.68
PMID:33461288
Diversity of beetles (Coleoptera) in natural and planted saxaul forests (Haloxylon ammodendron) in the South Gobi Desert, Mongolia Batchuluun B, Wunderlich J, Schmitt M Zookeys 03-Dec-2020
PMCID:PMC7728731
doi:10.3897/zookeys.1000.56856
PMID:33354135
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011

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 / Harmala alkaloids
Harmine 5280953 Click to see CC1=NC=CC2=C1NC3=C2C=CC(=C3)OC 212.25 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.1080/10286020701611636
https://doi.org/10.1016/S0031-9422(99)00440-9
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
3-Ethyl-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 102369826 Click to see CCC1=CC2=NC=CC3=C2N(C1=O)C4=C3C=CC(=C4)OC 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
9-Methoxy-5-methyl-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one 102369825 Click to see CC1=CC2=NC=CC3=C2N(C1=O)C4=C3C=CC(=C4)OC 264.28 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(4R)-4-hydroxy-3,4-dihydronaphthalene-2-carboxylic acid 162905794 Click to see C1C(C2=CC=CC=C2C=C1C(=O)O)O 190.19 unknown https://doi.org/10.1002/HLCA.201000252
3,4-Dihydro-4-hydroxynaphthalene-2-carboxylic acid 22367995 Click to see C1C(C2=CC=CC=C2C=C1C(=O)O)O 190.19 unknown https://doi.org/10.1002/HLCA.201000252
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3H-quinazolin-4-one 163187871 Click to see C1=CC=C2C(=C1)C(=O)NC(=N2)CCCOC3C(C(C(C(O3)CO)O)O)O 366.40 unknown https://doi.org/10.1002/HLCA.201000252
2-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3H-quinazolin-4-one 162977558 Click to see C1=CC=C2C(=C1)C(=O)NC(=N2)CCCOC3C(C(C(C(O3)CO)O)O)O 366.40 unknown https://doi.org/10.1002/HLCA.201000252
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(1aS,3S,7S,7aS,7bR)-1,1,7,7a-tetramethyl-2,3,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalen-3-ol 162850359 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3alpha)-3-(Acetyloxy)lup-20(29)-en-28-oic acid 51690441 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1021/NP990227B
(4aS,6aR,6aR,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-4a-methoxycarbonyl-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 10602594 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C(=O)O)C)C 542.70 unknown https://doi.org/10.1021/NP990227B
10-Acetyloxy-4a-methoxycarbonyl-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 85201737 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C(=O)O)C)C 542.70 unknown https://doi.org/10.1021/NP990227B
3-Acetoxy-27-hydroxy-20(29)-lupen-28-oic acid methyl ester 10649856 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC(=O)C)C)C(=O)OC 528.80 unknown https://doi.org/10.1021/NP990227B
3,27-Dihydroxy-20(29)-lupen-28-oic acid methyl ester 11799152 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)O)C)C(=O)OC 486.70 unknown https://doi.org/10.1021/NP990227B
9-Acetyloxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 289984 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.1021/NP990227B
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP990227B
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1021/NP990227B
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.1021/NP990227B
Epibetulinic acid 485711 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.1021/NP990227B
Methyl 9-acetyloxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 85219323 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC(=O)C)C)C(=O)OC 528.80 unknown https://doi.org/10.1021/NP990227B
Methyl 9-hydroxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 14707303 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)O)C)C(=O)OC 486.70 unknown https://doi.org/10.1021/NP990227B
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(12R)-12-methoxy-3,11,21-triazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one 162989615 Click to see COC1C2=CC3=CC=CC=C3N=C2C4=NC5=CC=CC=C5C(=O)N14 315.30 unknown https://doi.org/10.3987/COM-99-8595
(12S)-12-hydroxy-3,11,21-triazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one 162974567 Click to see C1=CC=C2C(=C1)C=C3C(N4C(=NC5=CC=CC=C5C4=O)C3=N2)O 301.30 unknown https://doi.org/10.3987/COM-97-S65
(3S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-ol 667496 Click to see C1CN2CC3=CC=CC=C3N=C2C1O 188.23 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.3987/COM-97-S65
1H-Pyrrolo[2,1-b]quinazolin-9-one, 3-hydroxy-2,3-dihydro- 10242 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O 202.21 unknown https://doi.org/10.3987/COM-97-S65
2-(1,2,3,9-Tetrahydropyrrolo[2,1-b]quinazolin-9-yl)acetic acid 101781770 Click to see C1CC2=NC3=CC=CC=C3C(N2C1)CC(=O)O 230.26 unknown https://doi.org/10.1002/HLCA.201000252
2-(3-hydroxypropyl)-1H-quinazolin-4-one 6325786 Click to see C1=CC=C2C(=C1)C(=O)N=C(N2)CCCO 204.22 unknown https://doi.org/10.3987/COM-99-8595
2-(quinoline-3-carbonyl)-1H-quinazolin-4-one 11771062 Click to see C1=CC=C2C(=C1)C=C(C=N2)C(=O)C3=NC(=O)C4=CC=CC=C4N3 301.30 unknown https://doi.org/10.3987/COM-99-8595
2-[(9R)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-9-yl]acetic acid 162894581 Click to see C1CC2=NC3=CC=CC=C3C(N2C1)CC(=O)O 230.26 unknown https://doi.org/10.1002/HLCA.201000252
CID 776133 776133 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O 202.21 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.3987/COM-97-S65
Deoxypeganine 442894 Click to see C1CC2=NC3=CC=CC=C3CN2C1 172.23 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.3987/COM-97-S65
Deoxyvasicinone 68261 Click to see C1CC2=NC3=CC=CC=C3C(=O)N2C1 186.21 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.3987/COM-97-S65
https://doi.org/10.1016/S0040-4039(98)02004-8
Luotonin A 10334120 Click to see C1C2=CC3=CC=CC=C3N=C2C4=NC5=CC=CC=C5C(=O)N41 285.30 unknown https://doi.org/10.3987/COM-97-S65
https://doi.org/10.1016/S0040-4039(99)00349-4
Luotonin B 10017730 Click to see C1=CC=C2C(=C1)C=C3C(N4C(=NC5=CC=CC=C5C4=O)C3=N2)O 301.30 unknown https://doi.org/10.1016/S0040-4039(99)00349-4
https://doi.org/10.3987/COM-97-S65
Luotonin E 11483874 Click to see COC1C2=CC3=CC=CC=C3N=C2C4=NC5=CC=CC=C5C(=O)N14 315.30 unknown https://doi.org/10.3987/COM-99-8595
Peganine 442929 Click to see C1CN2CC3=CC=CC=C3N=C2C1O 188.23 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.3987/COM-97-S65
Vasicine 72610 Click to see C1CN2CC3=CC=CC=C3N=C2C1O 188.23 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.3987/COM-97-S65
Vasicinone 442935 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O 202.21 unknown https://doi.org/10.3987/COM-97-S65
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
7-methoxy-4-methyl-9H-pyrido[3,4-b]indole 162888812 Click to see CC1=CN=CC2=C1C3=C(N2)C=C(C=C3)OC 212.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Organoheterocyclic compounds / Quinolines and derivatives
3-(1H-indol-3-yl)quinoline 10243546 Click to see C1=CC=C2C(=C1)C=C(C=N2)C3=CNC4=CC=CC=C43 244.29 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
3-Phenylquinoline 282849 Click to see C1=CC=C(C=C1)C2=CC3=CC=CC=C3N=C2 205.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
4-Quinolin-3-ylphenol 11746183 Click to see C1=CC=C2C(=C1)C=C(C=N2)C3=CC=C(C=C3)O 221.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxamides / Quinoline-3-carboxamides
Quinoline-3-carboxamide 15561101 Click to see C1=CC=C2C(=C1)C=C(C=N2)C(=O)N 172.18 unknown https://doi.org/10.3987/COM-99-8595
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(E)-3-(4-hydroxy-3,5-dimethoxycyclohexa-2,4-dien-1-yl)prop-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 129716090 Click to see COC1=C(C(=CC(C1)C=CCOC(=O)C=CC2=CC(=C(C=C2)O)OC)OC)O 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
[(E)-3-(4-hydroxy-5-methoxycyclohexa-2,4-dien-1-yl)prop-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 129716115 Click to see COC1=C(C=CC(C1)C=CCOC(=O)C=CC2=CC(=C(C=C2)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-hydroxy-3-methoxyphenyl)propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102369824 Click to see COC1=C(C=CC(=C1)CCCOC(=O)C=CC2=CC(=C(C=C2)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-Hydroxy-3-methoxyphenyl)propyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162864916 Click to see COC1=C(C=CC(=C1)CCCOC(=O)C=CC2=CC(=C(C=C2)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-hydroxy-3,5-dimethoxyphenyl)propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102369823 Click to see COC1=CC(=CC(=C1O)OC)CCCOC(=O)C=CC2=CC(=C(C=C2)O)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-Hydroxy-3,5-dimethoxyphenyl)propyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162963543 Click to see COC1=CC(=CC(=C1O)OC)CCCOC(=O)C=CC2=CC(=C(C=C2)O)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 71716455 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O 932.80 unknown https://doi.org/10.1007/S10600-010-9667-5
7-[3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 78157093 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O 932.80 unknown https://doi.org/10.1007/S10600-010-9667-5

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