pteleifoside G (BioDeep_00000395884)
Main id: BioDeep_00000018952
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C28H38O13 (582.2312297999999)
中文名称: (+)-南烛木树脂酚 9-O-葡萄糖甙
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O
InChI: InChI=1S/C28H38O13/c1-36-16-7-13(8-17(37-2)22(16)31)20-15(11-40-28-26(35)25(34)23(32)19(10-30)41-28)14(9-29)5-12-6-18(38-3)24(33)27(39-4)21(12)20/h6-8,14-15,19-20,23,25-26,28-35H,5,9-11H2,1-4H3/t14-,15-,19+,20+,23+,25-,26+,28+/m0/s1
描述信息
(+)-lyoniresinol-3-alpha-O-beta-D-glucopyranoside is a lignan that is (+)-lyoniresinol substituted by a beta-D-glucopyranosyl moiety at position 3 via a glycosidic linkage. Isolated from the root barks of Stemmadenia minima and Lycium chinense, it exhibits antimicrobial activities. It has a role as a metabolite, an antibacterial agent and an antifungal agent. It is a beta-D-glucoside, a dimethoxybenzene, a lignan, a primary alcohol, a monosaccharide derivative, a polyphenol and a member of tetralins. It is functionally related to a (+)-lyoniresinol.
(+)-lyoniresinol-3-alpha-O-beta-D-glucopyranoside is a natural product found in Barleria lupulina, Lycium chinense, and other organisms with data available.
A lignan that is (+)-lyoniresinol substituted by a beta-D-glucopyranosyl moiety at position 3 via a glycosidic linkage. Isolated from the root barks of Stemmadenia minima and Lycium chinense, it exhibits antimicrobial activities.
同义名列表
13 个代谢物同义名
(2R,3R,4S,5S,6R)-2-[[(1S,2R,3R)-1-(3,5-dimethoxy-4-oxidanyl-phenyl)-3-(hydroxymethyl)-6,8-dimethoxy-7-oxidanyl-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxy-phenyl)-6,8-dimethoxy-3-methylol-tetralin-2-yl]methoxy]-6-methylol-tetrahydropyran-3,4,5-triol; [(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methyl beta-D-glucopyranoside; (+)-lyoniresinol-3-alpha-O-beta-D-glucopyranoside; (+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside; (+)-Lyoniresinol 3|A-O-|A-D-glucopyranoside; (+)-lyoniresinol 9-O-beta-D-glucopyranoside; (+)-Lyoniresinol 3α-O-β-D-glucopyranoside; (+)-lyoniresinol-3a-O-β-glucoside; (+)-Lyoniresinol 9-O-glucoside; lyoniresinol glucoside; pteleifoside G
数据库引用编号
6 个数据库交叉引用编号
- ChEBI: CHEBI:66606
- PubChem: 10483388
- ChEMBL: CHEMBL464198
- CAS: 87585-32-8
- medchemexpress: HY-N0952
- MetaboLights: MTBLC66606
分类词条
相关代谢途径
Reactome(0)
BioCyc(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)
22 个相关的物种来源信息
- 241842 - Acanthus ebracteatus: 10.1016/S0031-9422(01)00306-5
- 328098 - Acanthus ilicifolius:
- 68527 - Aegle marmelos: 10.1248/CPB.42.1924
- 2918396 - Alangium premnifolium: 10.1016/S0031-9422(96)00879-5
- 82927 - Avicennia marina: 10.1055/S-2008-1034318
- 101743 - Barleria lupulina:
- 3505 - Betula pendula: 10.1016/S0960-894X(98)00528-9
- 78630 - Betula platyphylla: 10.1016/S0960-894X(98)00528-9
- 36622 - Chaenomeles sinensis:
- 136663 - Cordiera sessilis: 10.1590/S0103-50532007000700017
- 459629 - Embelia ribes: 10.1021/NP060284M
- 1818589 - Fernandoa adenophylla: 10.1016/S0031-9422(01)00212-6
- 345800 - Hovenia trichocarpa: 10.1016/S0031-9422(98)00409-9
- 112883 - Lycium chinense: 10.1007/BF02977397
- 1489749 - Markhamia stipulata: 10.1016/S0031-9422(01)00466-6
- 59982 - Myrsine africana: 10.1002/HLCA.200890234
- 32244 - Quillaja saponaria: 10.1016/0031-9422(95)00496-T
- 147244 - Stephania longa: 10.1248/CPB.58.415
- 222567 - Strobilanthes cusia: 10.1248/CPB.52.1242
- 326937 - Verbena brasiliensis: 10.1248/CPB.54.1421
- 1489958 - Walsura robusta: 10.1080/14786410902819152
- 2099542 - Zanthoxylum petiolare: 10.1016/S0031-9422(00)89656-9
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
- Chung Sub Kim, Lalita Subedi, Sun Yeou Kim, Sang Un Choi, Ki Hyun Kim, Kang Ro Lee. Lignan Glycosides from the Twigs of Chaenomeles sinensis and Their Biological Activities.
Journal of natural products.
2015 May; 78(5):1174-8. doi:
10.1021/acs.jnatprod.5b00090
. [PMID: 25894905] - Nguyen X Nhiem, Phan V Kiem, Chau V Minh, Nanyoung Kim, Seonju Park, Hwa Young Lee, Eun Sil Kim, Young Ho Kim, Sohyun Kim, Young-Sang Koh, Seung Hyun Kim. Diarylheptanoids and flavonoids from viscum album inhibit LPS-stimulated production of pro-inflammatory cytokines in bone marrow-derived dendritic cells.
Journal of natural products.
2013 Apr; 76(4):495-502. doi:
10.1021/np300490v
. [PMID: 23484668] - Pengcheng Lin, Shuai Li, Sujuan Wang, Yongchun Yang, Jiangong Shi. A nitrogen-containing 3-alkyl-1,4-benzoquinone and a gomphilactone derivative from Embelia ribes.
Journal of natural products.
2006 Nov; 69(11):1629-32. doi:
10.1021/np060284m
. [PMID: 17125236]