Salvigenin (BioDeep_00000270172)
Main id: BioDeep_00000017527
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C18H16O6 (328.0946836)
中文名称: 三裂鼠尾草素
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: COc(c3)ccc(c3)C(=C2)Oc(c1)c(C(=O)2)c(O)c(OC)c(OC)1
InChI: InChI=1S/C18H16O6/c1-21-11-6-4-10(5-7-11)13-8-12(19)16-14(24-13)9-15(22-2)18(23-3)17(16)20/h4-9,20H,1-3H3
描述信息
Salvigenin is a natural polyphenolic compound, with neuroprotective effect. Salvigenin has antitumor cytotoxic and immunomodulatory properties. Salvigenin inhibits H2O2-induced cell apoptosis[1][2].
Salvigenin is a natural polyphenolic compound, with neuroprotective effect. Salvigenin has antitumor cytotoxic and immunomodulatory properties. Salvigenin inhibits H2O2-induced cell apoptosis[1][2].
同义名列表
12 个代谢物同义名
4H-1-Benzopyran-4-one, 5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-; 5-Hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one; 5-Hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one; 5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-4-chromenone; 5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)chromen-4-one; 5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)chromone; 5-hydroxy-6,7,4-trimethoxyflavone; Salvigenin-d9; Salvigenin; 19103-54-9; 5-Hydroxy-6,7-dimethoxy-2- (4-methoxyphenyl) -4H-1-benzopyran-4-one; Psathyrotin
数据库引用编号
10 个数据库交叉引用编号
- ChEBI: CHEBI:192703
- PubChem: 161271
- Metlin: METLIN49591
- ChEMBL: CHEMBL376644
- KNApSAcK: C00003840
- CAS: 19103-54-9
- MoNA: TY000249
- PMhub: MS000107786
- Flavonoid: FL3FEANS0008
- medchemexpress: HY-N1318
分类词条
相关代谢途径
Reactome(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
111 个相关的物种来源信息
- 282720 - Achillea aspleniifolia: 10.1016/0031-9422(90)85371-L
- 359922 - Achillea formosa: 10.1515/ZNC-1989-3-423
- 282741 - Achillea impatiens: 10.1016/S0305-1978(98)00112-4
- 13329 - Achillea millefolium: 10.1016/0031-9422(90)85371-L
- 482483 - Achillea millefolium var. millefolium: 10.1016/0031-9422(90)85371-L
- 282760 - Achillea pseudopectinata: 10.1055/S-2007-969447
- 1028379 - Achillea santolina: 10.1016/S0031-9422(99)00054-0
- 282767 - Achillea setacea: 10.1016/0305-1978(88)90071-3
- 2029211 - Achillea sibirica: 10.1016/S0305-1978(98)00112-4
- 301866 - Achillea tenuifolia: 10.1016/S0031-9422(99)00054-0
- 301867 - Achillea vermicularis: 10.1016/0305-1978(91)90061-4
- 282770 - Achillea virescens:
- 282771 - Achillea wilhelmsii: 10.4268/CJCMM20150722
- 109063 - Alnus japonica: 10.1016/0031-9422(74)85049-1
- 925377 - Aloysia citrodora: 10.1055/S-2006-962505
- 436459 - Arnica acaulis: 10.1016/0031-9422(88)80605-8
- 149410 - Arnica longifolia: 10.1016/S0031-9422(00)89581-3
- 714449 - Artemisia anomala:
- 1227617 - Artemisia assoana: 10.1016/S0031-9422(00)83891-1
- 1473222 - Artemisia cina: 10.1007/BF00595086
- 401898 - Artemisia gmelinii: 10.1007/BF00595086
- 1123534 - Baccharis pedunculata: 10.1016/0031-9422(91)85145-P
- 315439 - Bellardia trixago: 10.3109/13880209009082777
- 3508 - Betula nigra: 10.1016/S0031-9422(00)86815-6
- 1550803 - Brickellia baccharidea: 10.1016/S0031-9422(00)98581-9
- 1550814 - Brickellia dentata: 10.1016/0031-9422(80)85136-3
- 168499 - Buddleja macrostachya: 10.1016/0378-8741(84)90075-8
- 204211 - Callicarpa americana: 10.1021/NP060534Z
- 124926 - Centaurea cineraria: 10.1016/0031-9422(88)80467-9
- 1048535 - Centaurea cuneifolia:
- 145508 - Centaurea ornata: 10.1021/NP50069A006
- 145513 - Centaurea raphanina: 10.1021/NP50021A025
- 2072395 - Centaurea scoparia: 10.1055/S-2006-959378
- 363453 - Centaurea spinosa:
- 558547 - Citrus deliciosa: 10.1248/CPB.41.714
- 85571 - Citrus reticulata: 10.1248/CPB.41.714
- 1281416 - Coleus hadiensis: 10.1002/HLCA.200490210
- 2485406 - Coleus sylvestris: 10.1021/NP030490J
- 312798 - Ferula aucheri: 10.1016/0031-9422(94)00840-P
- 211591 - Iphiona scabra: 10.1016/S0031-9422(00)81848-8
- 496633 - Jungia polita: 10.1016/0031-9422(92)83741-G
- 1241420 - Lantana fucata: 10.1021/NP9002383
- 980664 - Lepechinia caulescens: 10.1016/0031-9422(92)83466-C
- 301871 - Leucocyclus formosus: 10.1515/ZNC-1989-3-423
- 983213 - Liatris aspera: 10.1016/0031-9422(83)83036-2
- 102784 - Liatris elegans: 10.1080/14786410903027789
- 2291699 - Marrubium cylleneum: 10.1076/PHBI.40.4.245.8472
- 2291707 - Marrubium velutinum: 10.1016/J.PHYTOCHEM.2005.02.029
- 190902 - Mentha aquatica: 10.1016/S0031-9422(98)00672-4
- 650269 - Mentha aquatica var. citrata:
- 986249 - Mesosphaerum urticoides: 10.1016/0031-9422(91)83668-B
- 166995 - Montanoa leucantha: 10.1016/S0031-9422(00)89739-3
- 167007 - Montanoa tomentosa: 10.1016/0031-9422(91)85045-2
- 28940 - Nothofagus dombeyi: 10.1016/J.PHYTOCHEM.2004.04.002
- 204141 - Ocimum americanum:
- 39350 - Ocimum basilicum:
- 1224218 - Ocimum kilimandscharicum: 10.1016/S0031-9422(00)00439-8
- 204151 - Orthosiphon aristatus:
- 350585 - Osyris alba: 10.1080/10286020.2010.502892
- 542674 - Phyla dulcis:
- 33090 - Plants: -
- 306376 - Plectranthus fruticosus: 10.1021/NP030490J
- 1138119 - Pseudodictamnus hirsutus: 10.1021/NP50045A043
- 49207 - Salvia aethiopis:
- 268888 - Salvia amplexicaulis:
- 1933710 - Salvia caespitosa: 10.1080/10575630108041297
- 268896 - Salvia candidissima:
- 1685712 - Salvia ceratophylla: 10.1016/0031-9422(95)00416-5
- 268899 - Salvia chionopeplica:
- 95165 - Salvia columbariae:
- 1933716 - Salvia cyanescens:
- 207754 - Salvia dorrii: 10.1515/ZNC-1992-9-1025
- 268906 - Salvia fruticosa:
- 1933725 - Salvia heldreichiana:
- 392666 - Salvia hydrangea: 10.1021/NP200559C
- 1294397 - Salvia hypoleuca:
- 1520031 - Salvia lanigera:
- 49214 - Salvia lavandulifolia:
- 1685713 - Salvia limbata:
- 1571166 - Salvia macrosiphon:
- 226208 - Salvia miltiorrhiza:
- 1571167 - Salvia mirzayanii:
- 1585254 - Salvia moorcroftiana: 10.1078/094471102321621386
- 49215 - Salvia nemorosa: 10.1016/S0031-9422(00)90672-1
- 38868 - Salvia officinalis:
- 268920 - Salvia palaestina:
- 588964 - Salvia prionitis:
- 1933756 - Salvia sahendica:
- 38869 - Salvia sclarea: 10.1016/S0031-9422(00)90474-6
- 1685717 - Salvia syriaca:
- 1933761 - Salvia tchihatcheffii:
- 268912 - Salvia verbenaca:
- 1298553 - Salvia virgata:
- 1933767 - Salvia wiedemannii: 10.1016/0031-9422(91)83665-8
- 1933769 - Salvia yosgadensis:
- 457732 - Schistostephium crataegifolium: 10.1016/0031-9422(83)80100-9
- 65409 - Scutellaria baicalensis: 10.1248/YAKUSHI1947.104.5_529
- 403027 - Sideritis nutans: 10.1021/NP50057A027
- 1115765 - Tanacetum aucherianum: 10.1016/S0031-9422(96)00373-1
- 1854018 - Teucrium alyssifolium:
- 53177 - Teucrium flavum: 10.1016/S0031-9422(00)85039-6
- 1209860 - Teucrium heterophyllum: 10.1016/S0031-9422(00)90719-2
- 1423403 - Teucrium leucocladum: 10.1016/J.BSE.2003.12.009
- 1209871 - Teucrium massiliense: 10.1016/S0031-9422(00)85040-2
- 1117157 - Teucrium polium:
- 1209892 - Teucrium stocksianum: 10.1300/J044V03N01_03
- 201290 - Trichostema lanatum: 10.1515/ZNC-1992-9-1025
- 41657 - Ursinia nana: 10.1016/0031-9422(82)80131-3
- 49994 - Volkameria inermis:
- 396367 - 半枝莲: -
- 33090 - 黄芩: -
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Shih-Chung Yen, Liang-Chieh Chen, Han-Li Huang, Sin-Ting Ngo, Yi-Wen Wu, Tony Eight Lin, Tzu-Ying Sung, Ssu-Ting Lien, Hui-Ju Tseng, Shiow-Lin Pan, Wei-Jan Huang, Kai-Cheng Hsu. Investigation of Selected Flavonoid Derivatives as Potent FLT3 Inhibitors for the Potential Treatment of Acute Myeloid Leukemia.
Journal of natural products.
2021 01; 84(1):1-10. doi:
10.1021/acs.jnatprod.0c00589
. [PMID: 33393294] - Mahmoud A Al-Qudah, Hasan I Tashtoush, Ethar F Khlaifat, Sahar O Ibrahim, Ayman M Saleh, Hala I Al-Jaber, Musa H Abu Zarga, Sultan T Abu Orabi. Chemical constituents of the aerial parts of Salvia judaica Boiss. from Jordan.
Natural product research.
2020 Oct; 34(20):2981-2985. doi:
10.1080/14786419.2019.1597349
. [PMID: 31161797] - Melanie Deipenbrock, Andreas Hensel. Polymethoxylated flavones from Orthosiphon stamineus leaves as antiadhesive compounds against uropathogenic E. coli.
Fitoterapia.
2019 Nov; 139(?):104387. doi:
10.1016/j.fitote.2019.104387
. [PMID: 31678632] - Radhakrishnan Srivedavyasasri, Taylor Hayes, Samir A Ross. Phytochemical and biological evaluation of Salvia apiana.
Natural product research.
2017 Sep; 31(17):2058-2061. doi:
10.1080/14786419.2016.1269096
. [PMID: 28025900] - Sahar Mofidi Tabatabaei, Peyman Salehi, Mahdi Moridi Farimani, Markus Neuburger, Maria De Mieri, Matthias Hamburger, Samad Nejad-Ebrahimi. A nor-diterpene from Salvia sahendica leaves.
Natural product research.
2017 Aug; 31(15):1758-1765. doi:
10.1080/14786419.2017.1290619
. [PMID: 28278660] - Amer Tarawneh, Francisco León, Sara Pettaway, Khaled M Elokely, Michael L Klein, Janet Lambert, Arsala Mansoor, Stephen J Cutler. Flavonoids from Perovskia atriplicifolia and Their in Vitro Displacement of the Respective Radioligands for Human Opioid and Cannabinoid Receptors.
Journal of natural products.
2015 Jun; 78(6):1461-5. doi:
10.1021/acs.jnatprod.5b00218
. [PMID: 26035635] - Fatma Pinar Turkmenoglu, İpek Baysal, Samiye Ciftci-Yabanoglu, Kemal Yelekci, Hamdi Temel, Salih Paşa, Nurten Ezer, İhsan Çalış, Gulberk Ucar. Flavonoids from Sideritis Species: Human Monoamine Oxidase (hMAO) Inhibitory Activities, Molecular Docking Studies and Crystal Structure of Xanthomicrol.
Molecules (Basel, Switzerland).
2015 Apr; 20(5):7454-73. doi:
10.3390/molecules20057454
. [PMID: 25915461] - Anna Berim, Jeong-Jin Park, David R Gang. Unexpected roles for ancient proteins: flavone 8-hydroxylase in sweet basil trichomes is a Rieske-type, PAO-family oxygenase.
The Plant journal : for cell and molecular biology.
2014 Nov; 80(3):385-95. doi:
10.1111/tpj.12642
. [PMID: 25139498] - Elke H Heiss, Thi Van Anh Tran, Kristin Zimmermann, Stefan Schwaiger, Corina Vouk, Barbara Mayerhofer, Clemens Malainer, Atanas G Atanasov, Hermann Stuppner, Verena M Dirsch. Identification of chromomoric acid C-I as an Nrf2 activator in Chromolaena odorata.
Journal of natural products.
2014 Mar; 77(3):503-8. doi:
10.1021/np400778m
. [PMID: 24476568] - Burcu Çulhaoğlu, Gönül Yapar, Tuncay Dirmenci, Gülaçtı Topçu. Bioactive constituents of Salvia chrysophylla Stapf.
Natural product research.
2013 Mar; 27(4-5):438-47. doi:
10.1080/14786419.2012.734820
. [PMID: 23126495] - Z Habibi, Z Cheraghi, S Ghasemi, M Yousefi. A new highly hydroxylated triterpene from Salvia atropatana Bunge.
Natural product research.
2012; 26(20):1910-3. doi:
10.1080/14786419.2011.628668
. [PMID: 22017660] - Somayyeh Gandomkar, Maryam Yousefi, Zohreh Habibi, Mohammad Ali As'habi. A new triterpene from Salvia xanthocheila Boiss.
Natural product research.
2012; 26(7):648-53. doi:
10.1080/14786419.2010.541884
. [PMID: 21848491] - Megumi Furukawa, Mitsuko Makino, Emika Ohkoshi, Taketo Uchiyama, Yasuo Fujimoto. Terpenoids and phenethyl glucosides from Hyssopus cuspidatus (Labiatae).
Phytochemistry.
2011 Dec; 72(17):2244-52. doi:
10.1016/j.phytochem.2011.07.008
. [PMID: 21893325] - Catherine Argyropoulou, Anastasia Karioti, Helen Skaltsa. Minor labdane diterpenes from Marrubium thessalum.
Chemistry & biodiversity.
2011 Oct; 8(10):1880-90. doi:
10.1002/cbdv.201000215
. [PMID: 22006716] - Seed Niazmand, Maryam Esparham, Tahereh Hassannia, Mohammad Derakhshan. Cardiovascular effects of Teucrium polium L. extract in rabbit.
Pharmacognosy magazine.
2011 Jul; 7(27):260-4. doi:
10.4103/0973-1296.84244
. [PMID: 21969799] - Chia-Feng Kuo, Jeng-De Su, Chun-Hung Chiu, Chiung-Chi Peng, Chi-Huang Chang, Tzu-Ying Sung, Shiau-Huei Huang, Wen-Chin Lee, Charng-Cherng Chyau. Anti-inflammatory effects of supercritical carbon dioxide extract and its isolated carnosic acid from Rosmarinus officinalis leaves.
Journal of agricultural and food chemistry.
2011 Apr; 59(8):3674-85. doi:
10.1021/jf104837w
. [PMID: 21375325] - Naisheng Bai, Kan He, Marc Roller, Ching-Shu Lai, Xi Shao, Min-Hsiung Pan, Antoine Bily, Chi-Tang Ho. Flavonoid glycosides from Microtea debilis and their cytotoxic and anti-inflammatory effects.
Fitoterapia.
2011 Mar; 82(2):168-72. doi:
10.1016/j.fitote.2010.08.014
. [PMID: 20804824] - Ahmad R Gohari, Soodabeh Saeidnia, Maryam Malmir, Abbass Hadjiakhoondi, Yousef Ajani. Flavones and rosmarinic acid from Salvia limbata.
Natural product research.
2010 Dec; 24(20):1902-6. doi:
10.1080/14786411003766912
. [PMID: 21108116] - Muhammad Imran Ali, Zeeshan Ahmed, Alain Francois Kamdem Waffo, Muhammad Shaiq Ali. Flavonoids from Erythrina vogelii (Fabaceae) of Cameroon.
Natural product communications.
2010 Jun; 5(6):889-92. doi:
"
. [PMID: 20614816] - Mehdi Mohammadi, Maryam Yousefi, Zohreh Habibi, Abbas Shafiee. Two new coumarins from the chloroform extract of Angelica urumiensis from Iran.
Chemical & pharmaceutical bulletin.
2010 Apr; 58(4):546-8. doi:
10.1248/cpb.58.546
. [PMID: 20410639] - Roshan Patel, Naveen K Mahobia, Ravindra Gendle, Basant Kaushik, Sudarshan K Singh. Diuretic activity of leaves of Plectranthus amboinicus (Lour) Spreng in male albino rats.
Pharmacognosy research.
2010 Mar; 2(2):86-8. doi:
10.4103/0974-8490.62956
. [PMID: 21808546] - Ping Dong, Peiju Qiu, Yi Zhu, Shiming Li, Chi-Tang Ho, David Julian McClements, Hang Xiao. Simultaneous determination of four 5-hydroxy polymethoxyflavones by reversed-phase high performance liquid chromatography with electrochemical detection.
Journal of chromatography. A.
2010 Jan; 1217(5):642-7. doi:
10.1016/j.chroma.2009.11.097
. [PMID: 20022018] - Usama W Hawas, Amira M Gamal-Eldeen, Sayed A A El-Toumy, J J Marion Meyer, Ahmed A Hussein. Inhibition of the initiation stage of carcinogenesis by Salvia disermas constituents.
Zeitschrift fur Naturforschung. C, Journal of biosciences.
2009 Nov; 64(11-12):831-9. doi:
10.1515/znc-2009-11-1213
. [PMID: 20158154] - Hichem Henchiri, Bernard Bodo, Alexandre Deville, Lionel Dubost, Lazhar Zourgui, Aly Raies, Philippe Grellier, Lengo Mambu. Sesquiterpenoids from Teucrium ramosissimum.
Phytochemistry.
2009 Jul; 70(11-12):1435-41. doi:
10.1016/j.phytochem.2009.08.012
. [PMID: 19766274] - William P Jones, Tatiana Lobo-Echeverri, Qiuwen Mi, Hee-Byung Chai, Djaja D Soejarto, Geoffrey A Cordell, Steven M Swanson, A Douglas Kinghorn. Cytotoxic constituents from the fruiting branches of Callicarpa americana collected in southern Florida.
Journal of natural products.
2007 Mar; 70(3):372-7. doi:
10.1021/np060534z
. [PMID: 17279798] - Zheng-wen Yu, Hai-yan Zhu, Xiao-sheng Yang, Qian-yun Sun, Xiao-jiang Hao. [Study on chemical constituents from Incarvillea arguta and their accelerating PC-12 cell differentiation].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2005 Sep; 30(17):1335-8. doi:
. [PMID: 16323541]
- Masateru Ono, Hiroaki Morinaga, Chikako Masuoka, Tsuyoshi Ikeda, Masafumi Okawa, Junei Kinjo, Toshihiro Nohara. New Bisabolane-Type Sesquiterpenes from the Aerial Parts of Lippia dulcis.
Chemical & pharmaceutical bulletin.
2005 Sep; 53(9):1175-7. doi:
10.1248/cpb.53.1175
. [PMID: 16141591] - Roberto F Vieira, Renée J Grayer, Alan J Paton. Chemical profiling of Ocimum americanum using external flavonoids.
Phytochemistry.
2003 Jul; 63(5):555-67. doi:
10.1016/s0031-9422(03)00143-2
. [PMID: 12809716]