Marmesin (BioDeep_00000861000)
Main id: BioDeep_00000000059
Secondary id: BioDeep_00000000470, BioDeep_00000402960, BioDeep_00000863461
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C14H14O4 (246.0892044)
中文名称: 紫花前胡苷元, S-(+)-异紫花前胡内酯, S-(+)-印度枸橘素, S-(+)-印枳树皮素, S-(+)-印度榀椁素, 异紫花前胡内酯
谱图信息:
最多检出来源 Macaca mulatta(otcml) 0.43%
分子结构信息
SMILES: CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O
InChI: InChI=1S/C14H14O4/c1-14(2,16)12-6-9-5-8-3-4-13(15)18-10(8)7-11(9)17-12/h3-5,7,12,16H,6H2,1-2H3/t12-/m0/s1
描述信息
Nodakenetin is a marmesin with R-configuration. It has a role as a plant metabolite, a rat metabolite and a xenobiotic metabolite. It is an enantiomer of a (+)-marmesin.
Nodakenetin is a natural product found in Zanthoxylum beecheyanum, Melicope barbigera, and other organisms with data available.
A marmesin with R-configuration.
(+)-marmesin is a marmesin. It is an enantiomer of a nodakenetin.
Marmesin is a natural product found in Coronilla scorpioides, Clausena dunniana, and other organisms with data available.
Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2].
Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2].
S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.
S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.
S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.
同义名列表
80 个代谢物同义名
7H-Furo[3,2g][1]-benzopyran-7-one, (-2,3-dihydro-2-(1-hydroxy-1-hydroxymethylethyl)-, (R); 7H-FURO(3,2-G)(1)BENZOPYRAN-7-ONE, 2,3-DIHYDRO-2-(1-HYDROXY-1-METHYLETHYL)-, (2R)-; 7H-Furo(3,2-g)(1)benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (R)-; 7H-FURO(3,2-G)(1)BENZOPYRAN-7-ONE, 2,3-DIHYDRO-2-(1-HYDROXY-1-METHYLETHYL)-, (-)-; (R)-2-(1-Hydroxy-1-methylethyl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one; (2R)-2-(1-hydroxy-1-methylethyl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one; (R,S)-2-(1-Hydroxy-1-methyl-ethyl)-2,3-dihydro-furo[3,2-g]chromen-7-one; 2-(2-Hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one; (2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one; (R)-2-(2-Hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one; (2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one; 2-(2-Hydroxy-2-propanyl)-2,3-dihydro-7H-furo(3,2-g)chromen-7-one; marmesin, (R)-isomer; (R)-(-)-NODAKENETIN; (-)-Prangeferol; UNII-PKL4EW8LPQ; (-)-Marmesin; Prangeferol; Nodakenetic; Nodakenitin; nodakenetin; PKL4EW8LPQ; NODAKATIN; Marmesin; NANI; 7H-Furo[3,2-g][1]benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)-(+)-; 7H-Furo(3,2-g)(1)benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)-(+)-; 7H-FURO(3,2-G)(1)BENZOPYRAN-7-ONE, 2,3-DIHYDRO-2-(1-HYDROXY-1-METHYLETHYL)-, (2S)-; 7H-Furo[3,2-g][1]benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (2S)-; 7H-Furo[3,2-g][1]benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (+)-; (S)-(+)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one; 7H-Furo[3,2-g][1]benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)-; (2S)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one; (S)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one; (+)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one; (2S)-2-(1-hydroxy-1-methylethyl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one; 2-(1-Hydroxy-1-methylethyl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one #; (S)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one; (2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one; (2S)-2-(2-HYDROXYPROPAN-2-YL)-2H,3H,7H-FURO[3,2-G]CHROMEN-7-ONE; 7H-Furo[3, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)-(+)-; (S)-2-(2-Hydroxypropan-2-yl)-2H-furo[3,2-g]chromen-7(3H)-one; 2-(2-HYDROXYPROPAN-2-YL)-2H,3H,7H-FURO[3,2-G]CHROMEN-7-ONE; 7H-Furo[3, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (+)-; 7H-Furo[3, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)-; FWYSBEAFFPBAQU-LBPRGKRZSA-N; (+)-Marmesin;(S)-Marmesin; Marmesin ((+)-Marmesin); Spectrum2_000737; Spectrum3_001642; Spectrum4_001701; Spectrum5_000402; UNII-H5D33D6K5D; MARMESIN, (+)-; S-(+)-Marmesin; MEGxp0_001933; (7S)-marmesin; DivK1c_007014; S(+)-Marmesin; (+)-Marmesin; KBio2_007132; KBio3_002583; (S)-Marmesin; KBio1_001958; KBio2_001996; KBio2_004564; H5D33D6K5D; (2S)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one; (2S)-2-(1-hydroxy-1-methylethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one; SDCCGMLS-0066759.P001; Spectrum_001516; SpecPlus_000918; BSPBio_003363; KBioGR_002022; KBioSS_001996; ZINC00051924; SPBio_000694; 13849-08-6; NSC340840; C09276
数据库引用编号
27 个数据库交叉引用编号
- ChEBI: CHEBI:132623
- ChEBI: CHEBI:49083
- ChEBI: CHEBI:6695
- KEGG: C09278
- KEGG: C09276
- PubChem: 26305
- PubChem: 334704
- ChEMBL: CHEMBL1464240
- ChEMBL: CHEMBL442813
- Wikipedia: Marmesin
- MeSH: marmesin
- ChemIDplus: 0000495329
- ChemIDplus: 0013849086
- chemspider: 24509
- CAS: 495-32-9
- CAS: 13849-08-6
- medchemexpress: HY-N2276
- medchemexpress: HY-N2176
- MetaboLights: MTBLC132623
- PubChem: 11467
- KNApSAcK: C00000584
- 3DMET: B02821
- NIKKAJI: J14.029E
- PubChem: 11469
- KNApSAcK: C00002485
- 3DMET: B02823
- NIKKAJI: J15.206D
分类词条
相关代谢途径
Reactome(0)
PlantCyc(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)
174 个相关的物种来源信息
- 33090 紫花前胡: -
- 33090 石菖蒲: -
- 33090 北沙参: -
- 33090 羌活: -
- 312530 独活: -
- 49562 前胡: -
- 203717 防风: -
- 33090 知母: -
- 2099548 Zanthoxylum zanthoxyloides: 10.1021/NP50046A035
- 3494 Ficus carica: 10.1016/J.JEP.2008.06.025
- 159071 Zanthoxylum ailanthoides: 10.1016/J.BMC.2005.07.050
- 197987 Scaevola spinescens: 10.1055/S-2006-957961
- 49563 Peucedanum japonicum: 10.1016/0031-9422(95)00625-7
- 1752150 Zanthoxylum piasezkii: 10.1007/S10600-018-2544-3
- 159034 Clausena anisata: 10.1002/HLCA.200390259
- 1224754 Clausena dunniana: 10.1002/HLCA.200390259
- 241857 Antiaris toxicaria: 10.1016/J.BMC.2014.01.052
- 239644 Halosciastrum melanotilingia:
- 312530 Angelica pubescens:
- 52491 Angelica decursiva:
- 357970 Angelica biserrata:
- 2831626 Angelica pachycarpa:
- 48101 Angelica dahurica:
- 85712 Angelica gigas:
- 948492 Pleurospermum rivulorum: 10.1016/S0031-9422(97)00123-4
- 347984 Coronilla viminalis: 10.1055/S-2006-961611
- 390707 Coronilla vaginalis:
- 325744 Prangos uloptera:
- 1344466 Esenbeckia leiocarpa: 10.1002/CHIN.199005299
- 1620273 Brosimum gaudichaudii: 10.1590/S0103-50532002000200023
- 1585705 Prangos lipskyi: 10.1007/BF00570686
- 558542 Feroniella lucida: 10.1080/10286020.2011.572878
- 66391 Fatoua villosa: 10.1002/CBDV.200900326
- 241879 Fatoua pilosa: 10.1002/CBDV.200900326
- 48026 Ammi majus:
- 2927891 Peucedanum mashanense: 10.1055/S-0036-1596440
- 48119 Glehnia littoralis:
- 241889 Maquira calophylla:
- 118892 Coronilla scorpioides: 10.1076/PHBI.34.2.114.13188
- 231460 Afraegle paniculata: 10.1080/15287398409530517
- 76957 Chorilaena quercifolia: 10.1016/0031-9422(96)00355-X
- 52496 Prangos: 10.1007/BF00781092
- 1585712 Prangos tschimganica: 10.1248/CPB.49.877
- 681508 Zanthoxylum ekmanii: 10.1016/S0031-9422(00)91132-4
- 4043 Petroselinum crispum: 10.1016/S0031-9422(99)00072-2
- 463862 Ficus nervosa: 10.1002/CBDV.200900227
- 886265 Balanites aegyptiaca: 10.1055/S-2007-971481
- 1585704 Prangos latiloba:
- 282648 Asterolasia phebalioides: 10.1016/0305-1978(94)90036-1
- 265806 Angelica japonica: 10.1248/CPB.29.2565
- 675746 Thamnosma rhodesica: 10.1016/J.PHYTOCHEM.2003.12.020
- 159053 Limonia acidissima:
- 697043 Zanthoxylum wutaiense: 10.1002/CBDV.201000127
- 1764321 Boronia algida: 10.1016/0031-9422(94)00956-T
- 380075 Heracleum grandiflorum: 10.1007/BF02249699
- 68527 Aegle marmelos:
- 99506 Heracleum candicans: 10.1007/S11418-008-0266-8
- 2749842 Leionema ambiens: 10.1016/0031-9422(92)83450-D
- 282620 Rhadinothamnus anceps: 10.1016/0031-9422(92)83450-D
- 282633 Phebalium squamulosum: 10.1016/0031-9422(92)83450-D
- 357850 Angelica keiskei: 10.1016/0031-9422(90)85357-L
- 1585698 Prangos bucharica: 10.1007/BF00565847
- 37690 Citrus trifoliata: 10.1021/NP50048A044
- 172644 Broussonetia papyrifera: 10.1021/NP010288L
- 282619 Rhadinothamnus rudis:
- 1056465 Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
- 172644 Broussonetia papyrifera: 10.1016/0031-9422(94)00594-J
- 197987 Scaevola spinescens: 10.1055/S-2006-957961
- 2788934 Angelica glauca: 10.1080/10286020701273759
- 239644 Halosciastrum melanotilingia:
- 52491 Angelica decursiva:
- 48101 Angelica dahurica: 10.1016/J.PHYMED.2016.06.015
- 48026 Ammi majus: 10.1021/JO01060A039
- 282620 Rhadinothamnus anceps: 10.1016/0031-9422(92)83450-D
- 2749842 Leionema ambiens: 10.1016/0031-9422(92)83450-D
- 203717 Saposhnikovia divaricata:
- 165499 Hansenia forbesii: 10.1248/CPB.38.2498
- 54724 Hansenia weberbaueriana: 10.1248/CPB.38.2498
- 909277 Oreoseris gossypina: 10.1002/HLCA.200790013
- 1336615 Melicope barbigera: 10.1039/P19740001350
- 68527 Aegle marmelos: 10.1590/S0103-50532011000100024
- 1465234 Amyris elemifera: 10.3987/R-1981-06-0897
- 231460 Afraegle paniculata: 10.1016/0031-9422(73)85149-0
- 63039 Seseli peucedanoides: 10.1007/BF00579495
- 85712 Angelica gigas:
- 159053 Limonia acidissima: 10.1016/S0031-9422(00)84671-3
- 37690 Citrus trifoliata:
- 2099548 Zanthoxylum zanthoxyloides: 10.1021/NP50046A035
- 3494 Ficus carica: 10.1016/J.JEP.2008.06.025
- 159071 Zanthoxylum ailanthoides: 10.1016/J.BMC.2005.07.050
- 197987 Scaevola spinescens: 10.1055/S-2006-957961
- 49563 Peucedanum japonicum: 10.1016/0031-9422(95)00625-7
- 1752150 Zanthoxylum piasezkii: 10.1007/S10600-018-2544-3
- 159034 Clausena anisata: 10.1002/HLCA.200390259
- 1224754 Clausena dunniana: 10.1002/HLCA.200390259
- 241857 Antiaris toxicaria: 10.1016/J.BMC.2014.01.052
- 239644 Halosciastrum melanotilingia:
- 312530 Angelica pubescens:
- 52491 Angelica decursiva:
- 357970 Angelica biserrata:
- 2831626 Angelica pachycarpa:
- 48101 Angelica dahurica:
- 85712 Angelica gigas:
- 948492 Pleurospermum rivulorum: 10.1016/S0031-9422(97)00123-4
- 347984 Coronilla viminalis: 10.1055/S-2006-961611
- 390707 Coronilla vaginalis:
- 325744 Prangos uloptera:
- 1344466 Esenbeckia leiocarpa: 10.1002/CHIN.199005299
- 1620273 Brosimum gaudichaudii: 10.1590/S0103-50532002000200023
- 1585705 Prangos lipskyi: 10.1007/BF00570686
- 558542 Feroniella lucida: 10.1080/10286020.2011.572878
- 66391 Fatoua villosa: 10.1002/CBDV.200900326
- 241879 Fatoua pilosa: 10.1002/CBDV.200900326
- 48026 Ammi majus:
- 2927891 Peucedanum mashanense: 10.1055/S-0036-1596440
- 48119 Glehnia littoralis:
- 241889 Maquira calophylla:
- 118892 Coronilla scorpioides: 10.1076/PHBI.34.2.114.13188
- 231460 Afraegle paniculata: 10.1080/15287398409530517
- 76957 Chorilaena quercifolia: 10.1016/0031-9422(96)00355-X
- 52496 Prangos: 10.1007/BF00781092
- 1585712 Prangos tschimganica: 10.1248/CPB.49.877
- 681508 Zanthoxylum ekmanii: 10.1016/S0031-9422(00)91132-4
- 4043 Petroselinum crispum: 10.1016/S0031-9422(99)00072-2
- 463862 Ficus nervosa: 10.1002/CBDV.200900227
- 886265 Balanites aegyptiaca: 10.1055/S-2007-971481
- 1585704 Prangos latiloba:
- 282648 Asterolasia phebalioides: 10.1016/0305-1978(94)90036-1
- 265806 Angelica japonica: 10.1248/CPB.29.2565
- 675746 Thamnosma rhodesica: 10.1016/J.PHYTOCHEM.2003.12.020
- 159053 Limonia acidissima:
- 697043 Zanthoxylum wutaiense: 10.1002/CBDV.201000127
- 1764321 Boronia algida: 10.1016/0031-9422(94)00956-T
- 380075 Heracleum grandiflorum: 10.1007/BF02249699
- 68527 Aegle marmelos:
- 99506 Heracleum candicans: 10.1007/S11418-008-0266-8
- 2749842 Leionema ambiens: 10.1016/0031-9422(92)83450-D
- 282620 Rhadinothamnus anceps: 10.1016/0031-9422(92)83450-D
- 282633 Phebalium squamulosum: 10.1016/0031-9422(92)83450-D
- 357850 Angelica keiskei: 10.1016/0031-9422(90)85357-L
- 1585698 Prangos bucharica: 10.1007/BF00565847
- 37690 Citrus trifoliata: 10.1021/NP50048A044
- 172644 Broussonetia papyrifera: 10.1021/NP010288L
- 282619 Rhadinothamnus rudis:
- 1056465 Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
- 172644 Broussonetia papyrifera: 10.1016/0031-9422(94)00594-J
- 197987 Scaevola spinescens: 10.1055/S-2006-957961
- 2788934 Angelica glauca: 10.1080/10286020701273759
- 239644 Halosciastrum melanotilingia:
- 52491 Angelica decursiva:
- 48101 Angelica dahurica: 10.1016/J.PHYMED.2016.06.015
- 48026 Ammi majus: 10.1021/JO01060A039
- 282620 Rhadinothamnus anceps: 10.1016/0031-9422(92)83450-D
- 2749842 Leionema ambiens: 10.1016/0031-9422(92)83450-D
- 203717 Saposhnikovia divaricata:
- 165499 Hansenia forbesii: 10.1248/CPB.38.2498
- 54724 Hansenia weberbaueriana: 10.1248/CPB.38.2498
- 909277 Oreoseris gossypina: 10.1002/HLCA.200790013
- 1336615 Melicope barbigera: 10.1039/P19740001350
- 68527 Aegle marmelos: 10.1590/S0103-50532011000100024
- 1465234 Amyris elemifera: 10.3987/R-1981-06-0897
- 231460 Afraegle paniculata: 10.1016/0031-9422(73)85149-0
- 63039 Seseli peucedanoides: 10.1007/BF00579495
- 85712 Angelica gigas:
- 159053 Limonia acidissima: 10.1016/S0031-9422(00)84671-3
- 37690 Citrus trifoliata:
- 312530 Angelica pubescens Maxim.f. biserata Shan et Yuan: -
- 94219 Dendrobium nobile Lindl.: -
- 161865 Dendrobium chrysotoxum Lindl.: -
- 117953 Dendrobium fimbriatum Hook.: -
- 33090 Plants: -
- 48101 Angelica dahurica ( Fisch.ex Hoffm. ) Benth. et Hook.f.: -
- 48101 Angelica dahurica (Fisch.ex Hoffm.)Benth .et Hook.f.var.formosana(Boiss.)Shsn et Yuan: -
- 33090 Plants: -
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
- Zhaoxin Wang, Ying Zhou, Yuefei Wang, Xiaohui Yan. Reconstitution and Optimization of the Marmesin Biosynthetic Pathway in Yeast.
ACS synthetic biology.
2023 Sep; ?(?):. doi:
10.1021/acssynbio.3c00267
. [PMID: 37767718] - Ifeoma C Ezenyi, Jersley D Chirawurah, Nekpen Erhunse, Prakhar Agrawal, Dinkar Sahal, John O Igoli. Marmesin isolated from Celtis durandii Engl. root bioactive fraction inhibits β-hematin formation and contributes to antiplasmodial activity.
Journal of ethnopharmacology.
2023 Jun; 317(?):116804. doi:
10.1016/j.jep.2023.116804
. [PMID: 37352945] - C Hemakumar, B S Ravindranath, G A Ravishankar, D C Ramirez, S V Kiran. Marmesin and Marmelosin Interact with the Heparan Sulfatase-2 Active Site: Potential Mechanism for Phytochemicals from Bael Fruit Extract as Antitumor Therapeutics.
Oxidative medicine and cellular longevity.
2023; 2023(?):9982194. doi:
10.1155/2023/9982194
. [PMID: 36644581] - Yiqin Lin, Yingle Chen, Jingyang Zeng, Shunyuan Li. Nodakenetin Alleviates Inflammatory Pain Hypersensitivity by Suppressing NF-κB Signal Pathway.
Neuroimmunomodulation.
2022; 29(4):486-492. doi:
10.1159/000525690
. [PMID: 35995035] - Xiangyun Jian, Yucheng Zhao, Ziwen Wang, Shan Li, Li Li, Jun Luo, Lingyi Kong. Two CYP71AJ enzymes function as psoralen synthase and angelicin synthase in the biosynthesis of furanocoumarins in Peucedanum praeruptorum Dunn.
Plant molecular biology.
2020 Oct; 104(3):327-337. doi:
10.1007/s11103-020-01045-4
. [PMID: 32761540] - Ping Lei, Chushu Liao, Jianjun Chen, Ming Zhou. In vitro and in vivo growth inhibition of human leukemia cells by Nodakenetin are mediated via mitochondrial apoptosis, cell cycle arrest and inhibition of cell migration and invasion.
Journal of B.U.ON. : official journal of the Balkan Union of Oncology.
2019 May; 24(3):1219-1224. doi:
. [PMID: 31424682]
- Li-Shian Shi, Sheng-Chu Kuo, Han-Dong Sun, Susan L Morris-Natschke, Kuo-Hsiung Lee, Tian-Shung Wu. Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria.
Bioorganic & medicinal chemistry.
2014 Mar; 22(6):1889-98. doi:
10.1016/j.bmc.2014.01.052
. [PMID: 24582402] - Mahendra Jain, Rakhee Kapadia, Ravirajsinh N Jadeja, Menaka C Thounaojam, Ranjitsinh V Devkar, Shri H Mishra. Hepatoprotective activity of Feronia limonia root.
The Journal of pharmacy and pharmacology.
2012 Jun; 64(6):888-96. doi:
10.1111/j.2042-7158.2012.01481.x
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