(S)-Laudanosine (BioDeep_00000002519)
Main id: BioDeep_00000398001
Secondary id: BioDeep_00001868823
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite
代谢物信息卡片
化学式: C21H27NO4 (357.19399820000007)
中文名称: 劳丹素
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 26.09%
分子结构信息
SMILES: c12c(cc(c(c1)OC)OC)CCN([C@H]2Cc1ccc(c(c1)OC)OC)C
InChI: InChI=1S/C21H27NO4/c1-22-9-8-15-12-20(25-4)21(26-5)13-16(15)17(22)10-14-6-7-18(23-2)19(11-14)24-3/h6-7,11-13,17H,8-10H2,1-5H3
描述信息
(S)-Laudanosine is found in opium poppy. (S)-Laudanosine is an alkaloid from Papaver somniferum (opium poppy
Alkaloid from Papaver somniferum (opium poppy). (S)-Laudanosine is found in opium poppy.
D002491 - Central Nervous System Agents
DL-Laudanosine, an Atracurium and Cisatracurium metabolite, crosses the blood–brain barrier and may cause excitement and seizure activity[1].
DL-Laudanosine, an Atracurium and Cisatracurium metabolite, crosses the blood–brain barrier and may cause excitement and seizure activity[1].
同义名列表
数据库引用编号
21 个数据库交叉引用编号
- ChEBI: CHEBI:91599
- ChEBI: CHEBI:6389
- KEGG: C09558
- PubChem: 73397
- PubChem: 15548
- HMDB: HMDB0030213
- Metlin: METLIN1154
- ChEMBL: CHEMBL519894
- ChEMBL: CHEMBL1407
- MetaCyc: CPD-15741
- KNApSAcK: C00001876
- foodb: FDB002032
- chemspider: 14792
- CAS: 20412-65-1
- CAS: 2688-77-9
- CAS: 1699-51-0
- PMhub: MS000003151
- PubChem: 11749
- 3DMET: B03078
- NIKKAJI: J14.884I
- medchemexpress: HY-122489
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
33 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(33)
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-norlaudanine + SAM ⟶ (S)-tetrahydropapaverine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-norlaudanine + SAM ⟶ (S)-tetrahydropapaverine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
A + dihydropapaverine ⟶ A(H2) + papaverine
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-norlaudanine + SAM ⟶ (S)-tetrahydropapaverine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-norlaudanine + SAM ⟶ (S)-tetrahydropapaverine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
- papaverine biosynthesis:
A + dihydropapaverine ⟶ A(H2) + papaverine
- papaverine biosynthesis:
(S)-norlaudanine + SAM ⟶ (S)-tetrahydropapaverine + H+ + SAH
- papaverine biosynthesis:
(S)-laudanine + SAM ⟶ (S)-laudanosine + H+ + SAH
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
10 个相关的物种来源信息
- 1433312 - Berberis heteropoda: 10.1007/BF00631012
- 1439896 - Berberis nummularia: 10.1007/BF00630532
- 108409 - Cissampelos pareira: 10.1016/0031-9422(75)80388-8
- 56853 - Glaucium flavum: 10.1104/PP.15.01240
- 343270 - Guatteria amplifolia: 10.1055/S-2003-41126
- 651331 - Hazomalania voyronii: 10.1055/S-2006-957367
- 9606 - Homo sapiens: -
- 235797 - Huberantha cerasoides: 10.1021/NP070293A
- 357472 - Papaver macrostomum: 10.1080/13880200701538948
- 3469 - Papaver somniferum: 10.1016/S0021-9673(00)94605-3
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
- Zhihong Liu, Dane Huang, Shuangjia Zheng, Ying Song, Bingdong Liu, Jingyuan Sun, Zhangming Niu, Qiong Gu, Jun Xu, Liwei Xie. Deep learning enables discovery of highly potent anti-osteoporosis natural products.
European journal of medicinal chemistry.
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2018 May; 154(?):166-173. doi:
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