Bergapten (BioDeep_00000398015)

natural product PANOMIX_OTCML-2023

代谢物信息卡片

Bergapten

化学式: C12H8O4 (216.0422568)
中文名称: 佛手柑内酯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=C2C=CC(=O)OC2=CC3=C1C=CO3
InChI: InChI=1S/C12H8O4/c1-14-12-7-2-3-11(13)16-10(7)6-9-8(12)4-5-15-9/h2-6H,1H3

描述信息

D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use
D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.998
D000893 - Anti-Inflammatory Agents
D003879 - Dermatologic Agents
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.995
Acquisition and generation of the data is financially supported by the Max-Planck-Society
IPB_RECORD: 2841; CONFIDENCE confident structure
Bergapten is a natural anti-inflammatory and anti-tumor agent. Bergapten is inhibitory towards mouse and human CYP isoforms.
Bergapten is a natural anti-inflammatory and anti-tumor agent. Bergapten is inhibitory towards mouse and human CYP isoforms.

同义名列表

2 个代谢物同义名

Bergapten; 5-Methoxypsoralen

数据库引用编号

27 个数据库交叉引用编号

ChEBI: CHEBI:18293
KEGG: C01557
PubChem: 2355
DrugBank: DB12216
ChEMBL: CHEMBL24171
MeSH: 5-Methoxypsoralen
CAS: 484-20-8
MoNA: PM014607
MoNA: BML80817
MoNA: BML80815
MoNA: BML00719
MoNA: BML00710
MoNA: BML00701
MoNA: CE000162
MoNA: CE000161
MoNA: CE000160
MoNA: CE000159
MoNA: CE000158
MoNA: PB006145
MoNA: PB006144
MoNA: PB006143
PubChem: 4715
KNApSAcK: C00000575
3DMET: B00318
NIKKAJI: J12.563F
RefMet: Bergapten
medchemexpress: HY-N0370

分类词条

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)

170 个相关的物种来源信息

354485 - Acronychia pedunculata: 10.1016/0031-9422(89)80234-1
68527 - Aegle marmelos: 10.1078/094471103322004794
4456 - Alocasia macrorrhizos: 10.1007/S10600-008-9114-Z
48025 - Ammi: 10.1016/0041-5553(76)90065-3
48026 - Ammi majus:
40922 - Anethum graveolens:
55605 - Angelica acutiloba:
357845 - Angelica anomala: 10.1248/YAKUSHI1947.87.9_1118
40949 - Angelica archangelica:
48101 - Angelica dahurica:
52491 - Angelica decursiva:
85712 - Angelica gigas:
2788934 - Angelica glauca: 10.1080/10286020701273759
48115 - Angelica gmelinii: 10.1248/CPB.31.64
265806 - Angelica japonica:
357850 - Angelica keiskei:
46362 - Angelica lucida: 10.1248/CPB.31.64
312530 - Angelica pubescens:
1080328 - Angelica shikokiana: 10.1016/0378-8741(89)90033-0
165353 - Angelica sinensis:
2831629 - Angelica taiwaniana:
2831630 - Angelica tarokoensis: 10.1002/JCCS.197000012
357859 - Angelica ursina:
48027 - Anthriscus sylvestris: 10.1248/BPB.30.1340
4045 - Apium graveolens:
178647 - Arracacia tolucensis: 10.1016/J.JEP.2007.05.015
282648 - Asterolasia phebalioides: 10.1016/0305-1978(94)90036-1
339519 - Astragalus pycnocephalus: 10.1007/BF00598779
76951 - Atalantia ceylanica: 10.1016/S0031-9422(98)00638-4
886265 - Balanites aegyptiaca: 10.1055/S-2007-971481
53836 - Bituminaria bituminosa: 10.1139/B91-212
452763 - Boenninghausenia albiflora:
1620273 - Brosimum gaudichaudii:
489421 - Cachrys sicula: 10.1016/S0031-9422(00)85511-9
1108177 - Campylotropis hirtella: 10.1248/CPB.56.1338
47643 - Caragana frutex: 10.1007/BF00575186
48032 - Carum carvi: 10.1016/S0031-9422(00)81503-4
2706 - Citrus: 10.1002/JSFA.2979
37334 - Citrus maxima: 10.1016/S0021-9258(18)51679-3
171251 - Citrus medica:
37690 - Citrus trifoliata:
475932 - Citrus wilsonii: 10.1016/S0021-9258(18)51679-3
159034 - Clausena anisata: 10.1016/0031-9422(89)80056-1
48111 - Cnidium japonicum: 10.1016/S0031-9422(00)90538-7
94007 - Cnidium monnieri:
4047 - Coriandrum sativum: 10.1016/S0031-9422(00)81503-4
4039 - Daucus carota:
489439 - Deverra tortuosa:
298346 - Dictamnus albus:
354492 - Dinosperma melanophloium: 10.1016/S0305-1978(97)00116-6
2749845 - Dinosperma stipitatum: 10.1016/0031-9422(94)85101-8
241876 - Dorstenia arifolia:
382339 - Dorstenia bahiensis:
2604976 - Dorstenia barnimiana: 10.1016/S0031-9422(00)00419-2
984796 - Dorstenia brasiliensis:
984798 - Dorstenia cayapia: 10.1016/S0031-9422(00)00419-2
984801 - Dorstenia contrajerva:
984804 - Dorstenia drakena:
984806 - Dorstenia elliptica: 10.1016/J.PHYTOCHEM.2003.10.028
984809 - Dorstenia foetida: 10.1016/J.PHYTOCHEM.2011.03.008
984813 - Dorstenia lindeniana: 10.1016/S0031-9422(00)00419-2
2605001 - Dorstenia prorepens: 10.1016/S0031-9422(01)00483-6
106723 - Dorstenia psilurus: 10.1016/S0031-9422(00)00419-2
1136744 - Esenbeckia berlandieri: 10.1016/S0305-1978(01)00138-7
1654694 - Esenbeckia febrifuga: 10.1016/J.PHYMED.2008.02.001
1778592 - Euphorbia bivonae: 10.1007/S10600-011-0026-Y
241879 - Fatoua pilosa: 10.1002/CBDV.200900326
66391 - Fatoua villosa: 10.1002/CBDV.200900326
558542 - Feroniella lucida: 10.1080/10286020.2011.572878
3494 - Ficus carica:
182114 - Ficus glumosa: 10.1590/S0103-50532012000300015
66386 - Ficus pumila:
1118428 - Ficus tsjakela: 10.21608/BFSA.2001.65755
100580 - Ficus virens: 10.21608/BFSA.2001.65755
180113 - Garcinia parvifolia: 10.1021/NP8006364
48119 - Glehnia littoralis:
76967 - Glycosmis pentaphylla: 10.1016/S0031-9422(00)97490-9
239644 - Halosciastrum melanotilingia:
165499 - Hansenia forbesii:
54724 - Hansenia weberbaueriana:
63009 - Heracleum aconitifolium: 10.1007/BF00580082
380072 - Heracleum asperum:
99506 - Heracleum candicans: 10.1016/S0040-4020(01)82304-8
1162817 - Heracleum candolleanum: 10.1248/CPB.53.701
380073 - Heracleum dissectum:
380075 - Heracleum grandiflorum:
376866 - Heracleum lehmannianum: 10.1007/BF00570685
380076 - Heracleum leskovii: 10.1007/BF01134615
380077 - Heracleum mantegazzianum:
40918 - Heracleum maximum:
99507 - Heracleum moellendorffii: 10.1007/BF00563460
996940 - Heracleum moellendorffii var. paucivittatum: 10.1007/BF00600845
360621 - Heracleum persicum: 10.1016/S0031-9422(00)85242-5
376867 - Heracleum ponticum: 10.1007/BF00563460
692011 - Heracleum rapula: 10.1080/10286020290019677
40919 - Heracleum sphondylium:
542670 - Heracleum stevenii: 10.1111/J.1600-0536.1983.TB04386.X
692013 - Heracleum vicinum: 10.1248/CPB.53.701
473995 - Heracleum yungningense: 10.1248/CPB.53.701
2749842 - Leionema ambiens: 10.1016/0031-9422(92)83450-D
48042 - Levisticum officinale:
49551 - Ligusticum: 10.1016/0031-9422(75)85149-1
159053 - Limonia acidissima:
194324 - Maclura cochinchinensis: 10.1021/NP000406P
681588 - Magydaris pastinacea: 10.1021/NP50050A046
496675 - Meeboldia yunnanensis:
1487095 - Melicope borbonica: 10.1016/S0378-8741(98)00137-8
1487105 - Melicope denhamii: 10.1016/J.TET.2012.01.007
1336624 - Melicope latifolia: 10.1016/0031-9422(90)80154-9
1331801 - Metrodorea flavida: 10.1016/0031-9422(96)00232-4
549427 - Metrodorea nigra: 10.1016/0031-9422(95)00504-Z
2901850 - Murraya exotica: 10.1016/S0031-9422(00)97490-9
43711 - Murraya paniculata: 10.1016/S0031-9422(00)97490-9
354507 - Orixa japonica:
374961 - Paris dunniana: 10.1248/CPB.54.897
4041 - Pastinaca sativa:
4043 - Petroselinum crispum:
49563 - Peucedanum japonicum:
2927891 - Peucedanum mashanense: 10.1055/S-0036-1596440
203712 - Peucedanum officinale: 10.1007/BF02066241
52477 - Peucedanum ostruthium: 10.1016/S0031-9422(00)80344-1
1572681 - Peucedanum palustre: 10.1055/S-2006-961919
408989 - Peucedanum tauricum: 10.1016/J.PHYTOCHEM.2005.01.022
282637 - Phebalium filifolium: 10.1016/0031-9422(92)83450-D
282633 - Phebalium squamulosum: 10.1016/0031-9422(92)83450-D
354508 - Phellodendron chinense: 10.1139/B91-065
271192 - Pimpinella anisum:
40959 - Pimpinella saxifraga: 10.1007/BF00899143
33090 - Plants: -
948492 - Pleurospermum rivulorum: 10.1016/S0031-9422(97)00123-4
46147 - Portulaca oleracea: 10.1002/HLCA.201000250
1585705 - Prangos lipskyi: 10.1007/BF00570686
1585712 - Prangos tschimganica: 10.1248/CPB.49.877
325744 - Prangos uloptera:
884312 - Prionosciadium thapsoides: 10.1021/NP800387W
405848 - Psilopeganum sinense: 10.1016/0305-1978(88)90011-7
282620 - Rhadinothamnus anceps:
452790 - Ruta chalepensis:
37565 - Ruta graveolens:
675743 - Ruta macrophylla: 10.1007/BF00055511
266085 - Ruta montana:
452794 - Ruta pinnata: 10.1139/B93-109
23513 - Rutaceae: 10.1351/PAC200173030617
35974 - Santalum Album L\uff0e: -
203717 - Saposhnikovia divaricata:
1161150 - Scabiosa comosa:
491195 - Semenovia dasycarpa:
2502068 - Seseli dichotomum: 10.1016/S0040-4039(00)72373-2
460996 - Seseli mairei: 10.1016/S0040-4039(00)72373-2
63039 - Seseli peucedanoides: 10.1016/J.PHYTOCHEM.2005.01.022
2502079 - Seseli ponticum: 10.1016/S0040-4039(00)72373-2
223585 - Seseli tortuosum: 10.1016/S0040-4039(00)72373-2
496698 - Seseli yunnanense: 10.1016/S0040-4039(00)72373-2
210365 - Skimmia japonica: 10.1055/S-2006-962141
354518 - Skimmia laureola: 10.1016/S0031-9422(00)81759-8
354521 - Tetradium daniellii:
452800 - Thamnosma texana: 10.1016/S0031-9422(00)80348-9
63045 - Thysselinum palustre: 10.1055/S-2006-961919
491192 - Tordyliopsis brunonis: 10.1021/NP50048A034
489417 - Tordylium apulum: 10.1055/S-2006-957398
1898452 - Trichocline caulescens: 10.1016/S0031-9422(00)98112-3
3908 - Vicia sativa: 10.1007/BF00598366
159071 - Zanthoxylum ailanthoides:
2839963 - Zanthoxylum asiaticum: 10.1055/S-0034-1368568
1500039 - Zanthoxylum echinocarpum: 10.1021/NP800689B
1056472 - Zanthoxylum mayu:
354530 - Zanthoxylum schinifolium:
2714546 - Zanthoxylum tragodes: 10.1248/YAKUSHI1947.73.7_770
2099548 - Zanthoxylum zanthoxyloides: 10.1021/NP50046A035
94328 - Zingiber Officinale Roscoe: -

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

Tianshu Xu, Jiyuan Yin, Xuan Dai, Tianyuan Liu, Hanfen Shi, Yueyi Zhang, Shan Wang, Gaiyue Yue, Yanfei Zhang, Dandan Zhao, Sihua Gao, Marc Prentki, Lili Wang, Dongwei Zhang. Cnidii Fructus: A traditional Chinese medicine herb and source of antiosteoporotic drugs. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jun; 128(?):155375. doi: 10.1016/j.phymed.2024.155375. [PMID: 38507853]
Chong Gao, Zhong-He Hu, Zhen-Yu Cui, Yu-Chen Jiang, Jia-Yi Dou, Zhao-Xu Li, Li-Hua Lian, Ji-Xing Nan, Yan-Ling Wu. Angelica dahurica extract and its effective component bergapten alleviated hepatic fibrosis by activating FXR signaling pathway. Journal of natural medicines. 2024 Mar; 78(2):427-438. doi: 10.1007/s11418-024-01780-8. [PMID: 38334900]
Tong Luo, Xin Jia, Wan-di Feng, Jin-Yong Wang, Fang Xie, Ling-Dong Kong, Xue-Jiao Wang, Rui Lian, Xia Liu, Ying-Jie Chu, Yao Wang, An-Long Xu. Bergapten inhibits NLRP3 inflammasome activation and pyroptosis via promoting mitophagy. Acta pharmacologica Sinica. 2023 May; ?(?):. doi: 10.1038/s41401-023-01094-7. [PMID: 37142684]
Magdalena Bartnik. Efficient Separation of the Methoxyfuranocoumarins Peucedanin, 8-Methoxypeucedanin, and Bergapten by Centrifugal Partition Chromatography (CPC). Molecules (Basel, Switzerland). 2023 Feb; 28(4):. doi: 10.3390/molecules28041923. [PMID: 36838916]
Piseth Nhoek, Sungjin Ahn, Pisey Pel, Young-Mi Kim, Jungmoo Huh, Hyun Woo Kim, Minsoo Noh, Young-Won Chin. Alkaloids and Coumarins with Adiponectin-Secretion-Promoting Activities from the Leaves of Orixa japonica. Journal of natural products. 2023 01; 86(1):138-148. doi: 10.1021/acs.jnatprod.2c00844. [PMID: 36529937]
Noura S Dosoky, Prabodh Satyal, William N Setzer. Authentication of Citrus spp. Cold-Pressed Essential Oils by Their Oxygenated Heterocyclic Components. Molecules (Basel, Switzerland). 2022 Sep; 27(19):. doi: 10.3390/molecules27196277. [PMID: 36234812]
Kriti Juneja, Till Beuerle, Debabrata Sircar. Enhanced Accumulation of Biologically Active Coumarin and Furanocoumarins in Callus Culture and Field-grown Plants of Ruta chalepensis Through LED Light-treatment. Photochemistry and photobiology. 2022 09; 98(5):1100-1109. doi: 10.1111/php.13610. [PMID: 35191044]
Yanni Yang, Juanping Han, Renju G Lilly, Qin Yang, Yanjie Guo. Bergapten mediated inflammatory and apoptosis through AMPK/eNOS/AKT signaling pathway of isoproterenol-induced myocardial infarction in Wistar rats. Journal of biochemical and molecular toxicology. 2022 Sep; 36(9):e23143. doi: 10.1002/jbt.23143. [PMID: 35815753]
Muhammad Faheem, Arif-Ullah Khan, Muhammad Waqas Saleem, Fawad Ali Shah, Fawad Ali, Abdul Waheed Khan, Shupeng Li. Neuroprotective Effect of Natural Compounds in Paclitaxel-Induced Chronic Inflammatory Pain. Molecules (Basel, Switzerland). 2022 Aug; 27(15):. doi: 10.3390/molecules27154926. [PMID: 35956877]
Huan Shi, Ya-Qing Chang, Xie Feng, Gui-Ya Yang, Yu-Guang Zheng, Qian Zheng, Lan-Lan Zhang, Dan Zhang, Long Guo. Chemical comparison and discrimination of two plant sources of Angelicae dahuricae Radix, Angelica dahurica and Angelica dahurica var. formosana, by HPLC-Q/TOF-MS and quantitative analysis of multiple components by a single marker. Phytochemical analysis : PCA. 2022 Jul; 33(5):776-791. doi: 10.1002/pca.3129. [PMID: 35470493]
Maria Magdalena Quetglas-Llabrés, Cristina Quispe, Jesús Herrera-Bravo, Marcelo D Catarino, Olívia R Pereira, Susana M Cardoso, Kamal Dua, Dinesh Kumar Chellappan, Kavita Pabreja, Saurabh Satija, Meenu Mehta, Antoni Sureda, Miquel Martorell, Dinara Satmbekova, Balakyz Yeskaliyeva, Javad Sharifi-Rad, Naeem Rasool, Monica Butnariu, Iulia Cristina Bagiu, Radu Vasile Bagiu, Daniela Calina, William C Cho. Pharmacological Properties of Bergapten: Mechanistic and Therapeutic Aspects. Oxidative medicine and cellular longevity. 2022; 2022(?):8615242. doi: 10.1155/2022/8615242. [PMID: 35509838]
Christina L Burnett, Wilma F Bergfeld, Donald V Belsito, Ronald A Hill, Curtis D Klaassen, Daniel C Liebler, James G Marks, Ronald C Shank, Thomas J Slaga, Paul W Snyder, Lillian J Gill, Bart Heldreth. Safety Assessment of Citrus Plant- and Seed-Derived Ingredients as Used in Cosmetics. International journal of toxicology. 2021 12; 40(3_suppl):39S-52S. doi: 10.1177/10915818211040027. [PMID: 34406100]
Youdan Liang, Long Xie, Kai Liu, Yi Cao, Xiaolin Dai, Xian Wang, Jing Lu, Xumin Zhang, Xiaofang Li. Bergapten: A review of its pharmacology, pharmacokinetics, and toxicity. Phytotherapy research : PTR. 2021 Nov; 35(11):6131-6147. doi: 10.1002/ptr.7221. [PMID: 34347307]
Komal Latif, Arif-Ullah Khan, Muhammad Izhar Ul Haque, Komal Naeem. Bergapten Attenuates Nitroglycerin-Induced Migraine Headaches through Inhibition of Oxidative Stress and Inflammatory Mediators. ACS chemical neuroscience. 2021 09; 12(18):3303-3313. doi: 10.1021/acschemneuro.1c00146. [PMID: 34455773]
Shumaila Arshad, Maqsoodur Rehman, Juwairiya Zulfiqar, Saima Najam, Mulazim Hussain Asim, Farah Abid. Compatibility analysis of bergapten with different pharmaceutical excipients used in nanostructured lipid carriers. Pakistan journal of pharmaceutical sciences. 2019 Nov; 32(6(Supplementary)):2879-2885. doi: ". [PMID: 32024628]
Unwoo Kang, Ah-Reum Han, Yangkang So, Chang Hyun Jin, Seung Mok Ryu, Dongho Lee, Eun Kyoung Seo. Furanocoumarins from the Roots of Angelica dahurica with Inhibitory Activity against Intracellular Reactive Oxygen Species Accumulation. Journal of natural products. 2019 09; 82(9):2601-2607. doi: 10.1021/acs.jnatprod.9b00547. [PMID: 31464439]
Christina L Burnett, Monice M Fiume, Wilma F Bergfeld, Donald V Belsito, Ronald A Hill, Curtis D Klaassen, Daniel C Liebler, James G Marks, Ronald C Shank, Thomas J Slaga, Paul W Snyder, Lillian J Gill, Bart Heldreth. Safety Assessment of Citrus-Derived Peel Oils as Used in Cosmetics. International journal of toxicology. 2019 Sep; 38(2_suppl):33S-59S. doi: 10.1177/1091581819862504. [PMID: 31522650]
Gurjit Singh, Anudeep Kaur, Jashanpreet Kaur, Manpreet S Bhatti, Palwinder Singh, Rajbir Bhatti. Bergapten inhibits chemically induced nociceptive behavior and inflammation in mice by decreasing the expression of spinal PARP, iNOS, COX-2 and inflammatory cytokines. Inflammopharmacology. 2019 Aug; 27(4):749-760. doi: 10.1007/s10787-019-00585-6. [PMID: 30953227]
Gurjit Singh, Amritpal Singh, Palwinder Singh, Rajbir Bhatti. Bergapten Ameliorates Vincristine-Induced Peripheral Neuropathy by Inhibition of Inflammatory Cytokines and NFκB Signaling. ACS chemical neuroscience. 2019 06; 10(6):3008-3017. doi: 10.1021/acschemneuro.9b00206. [PMID: 31064179]
Yi He, Zeng Zisan, Zhenhui Lu, Li Zheng, Jinmin Zhao. Bergapten alleviates osteoarthritis by regulating the ANP32A/ATM signaling pathway. FEBS open bio. 2019 06; 9(6):1144-1152. doi: 10.1002/2211-5463.12648. [PMID: 31037830]
Guiping Chen, Qiang Xu, Min Dai, Xuqiang Liu. Bergapten suppresses RANKL-induced osteoclastogenesis and ovariectomy-induced osteoporosis via suppression of NF-κB and JNK signaling pathways. Biochemical and biophysical research communications. 2019 02; 509(2):329-334. doi: 10.1016/j.bbrc.2018.12.112. [PMID: 30579598]
Md Moshfekus Saleh-E-In, Ayan Roy, Muhammad Abdullah Al-Mansur, Choudhury Mahmood Hasan, Md Matiur Rahim, Nasim Sultana, Shamim Ahmed, Md Rabiul Islam, Johannes van Staden. Isolation and in silico prediction of potential drug-like compounds from Anethum sowa L. root extracts targeted towards cancer therapy. Computational biology and chemistry. 2019 Feb; 78(?):242-259. doi: 10.1016/j.compbiolchem.2018.11.025. [PMID: 30584950]
Shakti Prasad Pattanayak, Pritha Bose, Priyashree Sunita, Mohd Usman Mohd Siddique, Antonio Lapenna. Bergapten inhibits liver carcinogenesis by modulating LXR/PI3K/Akt and IDOL/LDLR pathways. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2018 Dec; 108(?):297-308. doi: 10.1016/j.biopha.2018.08.145. [PMID: 30227322]
Man Liao, Gengshen Song, Xiaoye Cheng, Xinpeng Diao, Yupeng Sun, Lantong Zhang. Simultaneous Determination of Six Coumarins in Rat Plasma and Metabolites Identification of Bergapten in Vitro and in Vivo. Journal of agricultural and food chemistry. 2018 May; 66(18):4602-4613. doi: 10.1021/acs.jafc.7b05637. [PMID: 29663811]
Yi Yang, Kangdi Zheng, Wenjie Mei, Yandong Wang, Chuqin Yu, Bangwei Yu, Shanbin Deng, Jinhua Hu. Anti-inflammatory and proresolution activities of bergapten isolated from the roots of Ficus hirta in an in vivo zebrafish model. Biochemical and biophysical research communications. 2018 02; 496(2):763-769. doi: 10.1016/j.bbrc.2018.01.071. [PMID: 29337062]
Prashant Joshi, Vinay R Sonawane, Ibidapo S Williams, Glen J P McCann, Linda Gatchie, Rajni Sharma, Naresh Satti, Bhabatosh Chaudhuri, Sandip B Bharate. Identification of karanjin isolated from the Indian beech tree as a potent CYP1 enzyme inhibitor with cellular efficacy via screening of a natural product repository. MedChemComm. 2018 Feb; 9(2):371-382. doi: 10.1039/c7md00388a. [PMID: 30108931]
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