Laudanine (BioDeep_00000003725)
Secondary id: BioDeep_00000014688, BioDeep_00000015507, BioDeep_00001870199
natural product PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C20H25NO4 (343.178349)
中文名称: 勞丹寧, 劳丹烷
谱图信息:
最多检出来源 Viridiplantae(plant) 1.49%
Last reviewed on 2024-08-20.
Cite this Page
Laudanine. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/laudanine (retrieved
2024-11-22) (BioDeep RN: BioDeep_00000003725). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC
InChI: InChI=1S/C20H25NO4/c1-21-8-7-14-11-19(24-3)20(25-4)12-15(14)16(21)9-13-5-6-18(23-2)17(22)10-13/h5-6,10-12,16,22H,7-9H2,1-4H3
描述信息
A benzyltetrahydroisoquinoline that is norlaudanosoline carrying four methyl substituents at positions N-1, O-6, O-7 and O-4.
Laudanine is a benzyltetrahydroisoquinoline that is norlaudanosoline carrying four methyl substituents at positions N-1, O-6, O-7 and O-4'. It is a benzyltetrahydroisoquinoline, a benzylisoquinoline alkaloid, a member of phenols and an aromatic ether. It is functionally related to a norlaudanosoline. It is a conjugate base of a laudanine(1+).
同义名列表
4 个代谢物同义名
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:76106
- ChEBI: CHEBI:76103
- ChEBI: CHEBI:76105
- KEGG: C17592
- KEGG: C09555
- PubChem: 92732
- PubChem: 442304
- ChEMBL: CHEMBL1425007
- MetaCyc: CPD-8924
- CAS: 85-64-3
- CAS: 3122-95-0
- CAS: 301-21-3
- MoNA: PM010806
- PMhub: MS000011155
- MetaboLights: MTBLC76103
- KNApSAcK: C00001875
- 3DMET: B03076
- NIKKAJI: J8.629K
- KNApSAcK: C00028453
- NIKKAJI: J358.586G
- NIKKAJI: J4.921B
- PubChem: 96023937
- KNApSAcK: 76103
- PubChem: 11746
- KNApSAcK: 76105
- LOTUS: LTS0102747
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)
33 个相关的物种来源信息
- 22140 - Annonaceae: LTS0102747
- 100370 - Croton: LTS0102747
- 518845 - Croton celtidifolius: 10.1055/S-2006-957745
- 518845 - Croton celtidifolius: LTS0102747
- 22027 - Cryptocarya: LTS0102747
- 2580221 - Cryptocarya amygdalina: 10.1016/S0031-9422(00)84175-8
- 2580221 - Cryptocarya amygdalina: LTS0102747
- 1619150 - Echinostephia aculeata: 10.1021/NP960381N
- 2759 - Eukaryota: LTS0102747
- 3977 - Euphorbiaceae: LTS0102747
- 56853 - Glaucium flavum: 10.1104/PP.15.01240
- 235797 - Huberantha cerasoides: 10.1021/NP070293A
- 3433 - Lauraceae: LTS0102747
- 3398 - Magnoliopsida: LTS0102747
- 3455 - Menispermaceae: LTS0102747
- 63801 - Ocotea: LTS0102747
- 128665 - Ocotea insularis: 10.1007/978-1-4899-1783-6_3
- 128665 - Ocotea insularis: LTS0102747
- 3468 - Papaver: LTS0102747
- 3469 - Papaver somniferum: 10.1073/PNAS.0405704101
- 3469 - Papaver somniferum: LTS0102747
- 3465 - Papaveraceae: LTS0102747
- 105756 - Polyalthia: 10.1021/NP070293A
- 147243 - Stephania: LTS0102747
- 1501469 - Stephania macrantha: 10.1021/NP960381N
- 1501474 - Stephania viridiflavens: 10.1016/J.PHYTOL.2011.11.001
- 1501474 - Stephania viridiflavens: LTS0102747
- 35493 - Streptophyta: LTS0102747
- 58023 - Tracheophyta: LTS0102747
- 33090 - Viridiplantae: LTS0102747
- 225838 - Xylopia: LTS0102747
- 992813 - Xylopia parviflora: 10.1016/J.PHYTOCHEM.2006.07.011
- 992813 - Xylopia parviflora: LTS0102747
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
- Isabel Desgagné-Penix, Morgan F Khan, David C Schriemer, Dustin Cram, Jacek Nowak, Peter J Facchini. Integration of deep transcriptome and proteome analyses reveals the components of alkaloid metabolism in opium poppy cell cultures.
BMC plant biology.
2010 Nov; 10(?):252. doi:
10.1186/1471-2229-10-252
. [PMID: 21083930] - Xu Han, Marc Lamshöft, Nadja Grobe, Xuan Ren, Anthony J Fist, Toni M Kutchan, Michael Spiteller, Meinhart H Zenk. The biosynthesis of papaverine proceeds via (S)-reticuline.
Phytochemistry.
2010 Aug; 71(11-12):1305-12. doi:
10.1016/j.phytochem.2010.04.022
. [PMID: 20494383] - Wenhua Cui, Kinuko Iwasa, Makiko Sugiura, Atsuko Takeuchi, Chisato Tode, Yumi Nishiyama, Masataka Moriyasu, Harukuni Tokuda, Kazuyoshi Takeda. Biotransformation of phenolic 1-benzyl-N-methyltetrahydroisoquinolines in plant cell cultures followed by LC/NMR, LC/MS, and LC/CD.
Journal of natural products.
2007 Nov; 70(11):1771-8. doi:
10.1021/np068060r
. [PMID: 17988098] - Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Ratsami Lekphrom. Bioactive constituents of the roots of Polyalthia cerasoides.
Journal of natural products.
2007 Sep; 70(9):1536-8. doi:
10.1021/np070293a
. [PMID: 17845001] - Nanae Fujii, Takayuki Inui, Kinuko Iwasa, Takashi Morishige, Fumihiko Sato. Knockdown of berberine bridge enzyme by RNAi accumulates (S)-reticuline and activates a silent pathway in cultured California poppy cells.
Transgenic research.
2007 Jun; 16(3):363-75. doi:
10.1007/s11248-006-9040-4
. [PMID: 17103244] - Susanne Frick, Julie A Chitty, Robert Kramell, Jürgen Schmidt, Robert S Allen, Philip J Larkin, Toni M Kutchan. Transformation of opium poppy (Papaver somniferum L.) with antisense berberine bridge enzyme gene (anti-bbe) via somatic embryogenesis results in an altered ratio of alkaloids in latex but not in roots.
Transgenic research.
2004 Dec; 13(6):607-13. doi:
10.1007/s11248-004-2892-6
. [PMID: 15672841] - Anan Ounaroon, Gabriele Decker, Jürgen Schmidt, Friedrich Lottspeich, Toni M Kutchan. (R,S)-Reticuline 7-O-methyltransferase and (R,S)-norcoclaurine 6-O-methyltransferase of Papaver somniferum - cDNA cloning and characterization of methyl transfer enzymes of alkaloid biosynthesis in opium poppy.
The Plant journal : for cell and molecular biology.
2003 Dec; 36(6):808-19. doi:
10.1046/j.1365-313x.2003.01928.x
. [PMID: 14675446]