tellimagrandin I (BioDeep_00000007961)

human metabolite PANOMIX_OTCML-2023

代谢物信息卡片

1-Desgalloyleugeniin

化学式: C34H26O22 (786.0915696)
中文名称:
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 95.83%

分子结构信息

SMILES: C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O
InChI: InChI=1S/C34H26O22/c35-12-1-8(2-13(36)21(12)41)30(47)55-28-27-18(53-34(51)29(28)56-31(48)9-3-14(37)22(42)15(38)4-9)7-52-32(49)10-5-16(39)23(43)25(45)19(10)20-11(33(50)54-27)6-17(40)24(44)26(20)46/h1-6,18,27-29,34-46,51H,7H2/t18-,27-,28+,29-,34?/m1/s1

描述信息

同义名列表

3 个代谢物同义名

1-Desgalloyleugeniin; tellimagrandin I; SCHEMBL17148971

数据库引用编号

13 个数据库交叉引用编号

ChEBI: CHEBI:9433
KEGG: C10241
PubChem: 5153915
PubChem: 442690
HMDB: HMDB0136068
Metlin: METLIN68192
ChEMBL: CHEMBL4569642
KNApSAcK: C00002938
CAS: 79786-08-6
PMhub: MS000021485
PubChem: 12427
3DMET: B05425
NIKKAJI: J339.288K

分类词条

单宁和没食子酰衍生物

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)

63 个相关的物种来源信息

627158 Eucalyptus robusta: 10.1016/0031-9422(93)85448-Z
74645 Rosa rugosa: 10.1007/S11418-010-0418-5
219868 Syzygium aromaticum: 10.1055/S-2001-11993
375273 Pimenta pseudocaryophyllus: 10.1055/S-2001-11993
189799 Tamarix nilotica: 10.1021/NP900829G
2544982 Tamarix senegalensis: 10.1021/NP900829G
22663 Punica granatum: 10.1248/BPB.16.787
1310070 Tamarix pakistanica: 10.1248/CPB.39.2849
87674 Eucalyptus nitens: 10.1002/PCA.548
714648 Rubus cochinchinensis: 10.1016/0031-9422(92)83451-4
74656 Agrimonia pilosa: 10.1016/0031-9422(92)83451-4
74645 Rosa rugosa:
1769920 Filipendula camtschatica: 10.1016/0031-9422(92)83451-4
176125 Agrimonia nipponica: 10.1016/0031-9422(92)83451-4
148907 Sieversia pentapetala: 10.1016/0031-9422(92)83451-4
211815 Rubus plicatus: 10.1016/0031-9422(92)83451-4
212836 Euphorbia prostrata: 10.1248/CPB.42.2005
1046480 Euphorbia makinoi: 10.1248/CPB.42.2005
714473 Geum aleppicum:
16922 Camptotheca acuminata: 10.1248/CPB.36.2017
38787 Betula pubescens: 10.1016/S0031-9422(00)00502-1
321607 Geum japonicum: 10.1016/S0031-9422(00)83179-9
32229 Geum macrophyllum: 10.1016/S0031-9422(00)83179-9
253221 Alnus sieboldiana: 10.1248/CPB.37.2655
385388 Camellia oleifera: 10.1248/CPB.38.2681
182300 Camellia sasanqua: 10.1248/CPB.38.2681
4443 Camellia japonica: 10.1248/CPB.38.2681
16906 Cornus officinalis: 10.1248/CPB.37.2665
85277 Stachyurus praecox: 10.1248/CPB.39.1689
482428 Oenothera glazioviana: 10.1039/P19900002735
58331 Quercus suber: 10.1021/NP010465I
627158 Eucalyptus robusta: 10.1016/0031-9422(93)85448-Z
74645 Rosa rugosa: 10.1007/S11418-010-0418-5
219868 Syzygium aromaticum: 10.1055/S-2001-11993
375273 Pimenta pseudocaryophyllus: 10.1055/S-2001-11993
189799 Tamarix nilotica: 10.1021/NP900829G
2544982 Tamarix senegalensis: 10.1021/NP900829G
22663 Punica granatum: 10.1248/BPB.16.787
1310070 Tamarix pakistanica: 10.1248/CPB.39.2849
87674 Eucalyptus nitens: 10.1002/PCA.548
714648 Rubus cochinchinensis: 10.1016/0031-9422(92)83451-4
74656 Agrimonia pilosa: 10.1016/0031-9422(92)83451-4
74645 Rosa rugosa:
1769920 Filipendula camtschatica: 10.1016/0031-9422(92)83451-4
176125 Agrimonia nipponica: 10.1016/0031-9422(92)83451-4
148907 Sieversia pentapetala: 10.1016/0031-9422(92)83451-4
211815 Rubus plicatus: 10.1016/0031-9422(92)83451-4
212836 Euphorbia prostrata: 10.1248/CPB.42.2005
1046480 Euphorbia makinoi: 10.1248/CPB.42.2005
714473 Geum aleppicum:
16922 Camptotheca acuminata: 10.1248/CPB.36.2017
38787 Betula pubescens: 10.1016/S0031-9422(00)00502-1
321607 Geum japonicum: 10.1016/S0031-9422(00)83179-9
32229 Geum macrophyllum: 10.1016/S0031-9422(00)83179-9
253221 Alnus sieboldiana: 10.1248/CPB.37.2655
385388 Camellia oleifera: 10.1248/CPB.38.2681
182300 Camellia sasanqua: 10.1248/CPB.38.2681
4443 Camellia japonica: 10.1248/CPB.38.2681
16906 Cornus officinalis: 10.1248/CPB.37.2665
85277 Stachyurus praecox: 10.1248/CPB.39.1689
482428 Oenothera glazioviana: 10.1039/P19900002735
58331 Quercus suber: 10.1021/NP010465I
9606 Homo sapiens: -

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

M Tolmie, M J Bester, J C Serem, M Nell, Z Apostolides. The potential antidiabetic properties of green and purple tea [Camellia sinensis (L.) O Kuntze], purple tea ellagitannins, and urolithins. Journal of ethnopharmacology. 2023 Jun; 309(?):116377. doi: 10.1016/j.jep.2023.116377. [PMID: 36907477]
Shota Machida, Saki Mukai, Rina Kono, Megumi Funato, Hiroaki Saito, Taketo Uchiyama. Synthesis and Comparative Structure-Activity Study of Carbohydrate-Based Phenolic Compounds as α-Glucosidase Inhibitors and Antioxidants. Molecules (Basel, Switzerland). 2019 Nov; 24(23):. doi: 10.3390/molecules24234340. [PMID: 31783621]
Jun Yin, In Hyoek Hwang, Min Won Lee. Anti-acne vulgaris effect including skin barrier improvement and 5α-reductase inhibition by tellimagrandin I from Carpinus tschonoskii. BMC complementary and alternative medicine. 2019 Nov; 19(1):323. doi: 10.1186/s12906-019-2734-y. [PMID: 31752827]
Divya Ganesan, Eman Al-Sayed, Abhishek Albert, Eldho Paul, Abdel Nasser B Singab, Selvam Govindan Sadasivam, Luciano Saso. Antioxidant activity of phenolic compounds from extracts of Eucalyptus globulus and Melaleuca styphelioides and their protective role on D-glucose-induced hyperglycemic stress and oxalate stress in NRK-49Fcells. Natural product research. 2018 Jun; 32(11):1274-1280. doi: 10.1080/14786419.2017.1343324. [PMID: 28637361]
Nicolas Baert, Jorma Kim, Maarit Karonen, Juha-Pekka Salminen. Inter-population and inter-organ distribution of the main polyphenolic compounds of Epilobium angustifolium. Phytochemistry. 2017 Feb; 134(?):54-63. doi: 10.1016/j.phytochem.2016.11.003. [PMID: 27866749]
Mohamed A A Orabi, Shoko Taniguchi, Hiroshi Sakagami, Morio Yoshimura, Yoshiaki Amakura, Tsutomu Hatano. Hydrolyzable Tannins of Tamaricaceous Plants. 7.1 Structures and Cytotoxic Properties of Oligomeric Ellagitannins from Leaves of Tamarix nilotica and Cultured Tissues of Tamarix tetrandra. Journal of natural products. 2016 Apr; 79(4):984-95. doi: 10.1021/acs.jnatprod.5b01065. [PMID: 26938659]
Juha-Pekka Salminen, Alexander N Shikov, Maarit Karonen, Olga N Pozharitskaya, Jorma Kim, Valery G Makarov, Raimo Hiltunen, Bertalan Galambosi. Rapid profiling of phenolic compounds of green and fermented Bergenia crassifolia L. leaves by UPLC-DAD-QqQ-MS and HPLC-DAD-ESI-QTOF-MS. Natural product research. 2014; 28(19):1530-3. doi: 10.1080/14786419.2014.923999. [PMID: 24896228]
Keiji Funatogawa, Shunji Hayashi, Hirofumi Shimomura, Takashi Yoshida, Tsutomu Hatano, Hideyuki Ito, Yoshikazu Hirai. Antibacterial activity of hydrolyzable tannins derived from medicinal plants against Helicobacter pylori. Microbiology and immunology. 2004; 48(4):251-61. doi: 10.1111/j.1348-0421.2004.tb03521.x. [PMID: 15107535]
Eva Leu, Anja Krieger-Liszkay, Charilaos Goussias, Elisabeth M Gross. Polyphenolic allelochemicals from the aquatic angiosperm Myriophyllum spicatum inhibit photosystem II. Plant physiology. 2002 Dec; 130(4):2011-8. doi: 10.1104/pp.011593. [PMID: 12481084]
S Shiota, M Shimizu, T Mizusima, H Ito, T Hatano, T Yoshida, T Tsuchiya. Restoration of effectiveness of beta-lactams on methicillin-resistant Staphylococcus aureus by tellimagrandin I from rose red. FEMS microbiology letters. 2000 Apr; 185(2):135-8. doi: 10.1111/j.1574-6968.2000.tb09051.x. [PMID: 10754237]
Z X Jin, G Yang, Y A Piao. [Chemical constituents of tannin in Filipendula palmata Pall]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 1994 Jan; 19(1):32-3, 62. doi: ". [PMID: 8011121]