Canadine (BioDeep_00000017214)

Main id: BioDeep_00000000840

 

human metabolite PANOMIX_OTCML-2023 blood metabolite


代谢物信息卡片


(1S)-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.0^{2,10.0^{4,8.0^{15,20]henicosa-2,4(8),9,15(20),16,18-hexaene

化学式: C20H21NO4 (339.1471)
中文名称: 四氢小檗碱, (s)-四氢小檗碱
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC
InChI: InChI=1S/C20H21NO4/c1-22-17-4-3-12-7-16-14-9-19-18(24-11-25-19)8-13(14)5-6-21(16)10-15(12)20(17)23-2/h3-4,8-9,16H,5-7,10-11H2,1-2H3

描述信息

Canadine is a berberine alkaloid that is 5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline substituted by methoxy groups at positions 9 and 10. It is a berberine alkaloid, an organic heteropentacyclic compound, an aromatic ether and an oxacycle.
Canadine is a natural product found in Glaucium squamigerum, Hydrastis canadensis, and other organisms with data available.
A berberine alkaloid that is 5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline substituted by methoxy groups at positions 9 and 10.
D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors
D002317 - Cardiovascular Agents > D002121 - Calcium Channel Blockers
D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents
D000077264 - Calcium-Regulating Hormones and Agents
D049990 - Membrane Transport Modulators
Tetrahydroberberine is an isoquinoline alkaloid isolated from Corydalis Corydalis, with uM-level affinity for D2 and 5-HT1A receptors.
Tetrahydroberberine is a different kind of living thing that can be extended and divided into parts. Tetrahydroberberine is a kind of effective D2 receptor antagonistic force. Tetrahydroberberine has the ability to strengthen the stomach and relieve the pressure on the stomach[1][2][3].
Tetrahydroberberine is an isoquinoline alkaloid isolated from Corydalis Corydalis, with uM-level affinity for D2 and 5-HT1A receptors.

同义名列表

63 个代谢物同义名

(1S)-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.0^{2,10.0^{4,8.0^{15,20]henicosa-2,4(8),9,15(20),16,18-hexaene; 16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.0(2),(1)?.0?,?.0(1)?,(2)?]henicosa-2,4(8),9,15(20),16,18-hexaene; 16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.0^{2,10.0^{4,8.0^{15,20]henicosa-2,4(8),9,15(20),16,18-hexaene; 16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaene; 10-METHOXY-5,8,13,13A-TETRAHYDRO-6H-[1,3]DIOXOLO[4,5-G]ISOQUINO[3,2-A]ISOQUINOLIN-9-YL METHYL ETHER; Isoquinolino[2,1-b]isoquinoline, 5,6,7,8,13,13a-hexahydro-2,3-methylenedioxy-9,10-dimethoxy-; 9,10-bis(methyloxy)-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline; 9,10-Dimethoxy-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline #; 9,10-Dimethoxy-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline; 6H-Benzo[g]-1,3-benzodioxolo[5,6-a]quinolizine, 5,8,13,13a-tetrahydro-9,10-dimethoxy-; 6H-Benzo(g)-1,3-benzodioxolo(5,6-a)quinolizine, 5,8,13,13a-tetrahydro-9,10-dimethoxy-; 6H-Benzo[g]-1,3-benzodioxolo[5,6-a]quinolizine,5,8,13,13a-tetrahydro-9,10-dimethoxy-; 5,8,13,13a-tetrahydro-9,10-dimethoxy-6H-benzo(g)-1,3-benzodioxolo(5,6-a)quinolizine; 5,8,13,13a-Tetrahydro-9,10-dimethoxy-6H-benzo(g)benzo-1,3-dioxolo(5,6-a)quinolizine; 5,8,13,13a-Tetrahydro-9,10-dimethoxy-6H-benzo[g]benzo-1,3-dioxolo[5,6-a]quinolizine; 6H-Benzo[g]-1,6-a]quinolizine, 5,8,13,13a-tetrahydro-9,10,dimethoxy-, (.+-.)-; 6H-Benzo[g]-1,6-a]quinolizine, 5,8,13,13a-tetrahydro-9,10-dimethoxy-; Berbine,10-dimethoxy-2,3-(methylenedioxy)-, (.+-.)-; Berbine, 9,10-dimethoxy-2,3-(methylenedioxy)-; 9,10-Dimethoxy-2,3-(methylenedioxy)berbine; Berbine,10-dimethoxy-2,3-(methylenedioxy)-; VZTUIEROBZXUFA-UHFFFAOYSA-N; (.+-.)-Tetrahydroberberine; (d,l)-Tetrahydroberberine; (+-)-Tetrahydroberberin; Tetrahydroberberine,THB; Tetrahydroberberine THB; dl-Tetrahydroberberine; Berberine, tetrahydro-; canadine hydrochloride; canadine, (+-)-isomer; CANADINE DL-FORM [MI]; canadine, (S)-isomer; canadine, (R)-isomer; Tetrahydroberberine; Prestwick2_000672; Prestwick1_000672; Canadine, (.+-.)-; Prestwick0_000672; Prestwick3_000672; (.+/-.)-Canadine; CANADINE, (+/-)-; Canadine dl-form; (.+-.)-Canadine; UNII-V2SSH085X8; CANADINE (DL-); (+/-)-Canadine; Tox21_110451_1; TimTec1_005946; CANADINE [MI]; Xanthopuccine; (+-)-Canadine; Oprea1_387569; BPBio1_000841; Oprea1_388593; NCI60_042115; Tox21_110451; NCI60_003328; dl-Canadine; V2SSH085X8; Canadine; Canadin; (S)-Canadine



数据库引用编号

18 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(1)

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)

29 个相关的物种来源信息

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。

亚细胞结构定位 关联基因列表
Cytoplasm 7 ABCB1, CA1, CYP2E1, ELANE, FBXO32, MAPK14, XDH
Peripheral membrane protein 3 ACHE, CYP1B1, CYP2E1
Endoplasmic reticulum membrane 3 CYP1A2, CYP1B1, CYP2E1
Nucleus 6 ACHE, DDX53, FBXO32, LIG4, MAGEA3, MAPK14
cytosol 6 CA1, DDX53, ELANE, FBXO32, MAPK14, XDH
dendrite 2 DRD2, P2RY1
phagocytic vesicle 1 ELANE
nucleoplasm 4 DDX53, FBXO32, LIG4, MAPK14
Cell membrane 5 ABCB1, ACHE, DRD2, P2RY1, P2RY12
Multi-pass membrane protein 5 ABCB1, CACNA1I, DRD2, P2RY1, P2RY12
Golgi apparatus membrane 1 DRD2
Synapse 2 ACHE, DRD2
cell surface 5 ABCB1, ACHE, ELANE, P2RY1, P2RY12
glutamatergic synapse 3 DRD2, MAPK14, P2RY1
Golgi apparatus 1 ACHE
Golgi membrane 1 DRD2
mitochondrial inner membrane 1 CYP2E1
neuromuscular junction 1 ACHE
presynaptic membrane 1 DRD2
acrosomal vesicle 1 DRD2
plasma membrane 8 ABCB1, ACHE, BCHE, CACNA1I, DRD2, F2, P2RY1, P2RY12
synaptic vesicle membrane 1 DRD2
Membrane 5 ABCB1, ACHE, CACNA1I, CYP1B1, P2RY12
apical plasma membrane 2 ABCB1, P2RY1
axon 1 DRD2
basolateral plasma membrane 1 P2RY1
extracellular exosome 4 ABCB1, CA1, ELANE, F2
endoplasmic reticulum 1 MAGEA3
extracellular space 5 ACHE, BCHE, ELANE, F2, XDH
perinuclear region of cytoplasm 1 ACHE
mitochondrion 2 CYP1B1, MAPK14
intracellular membrane-bounded organelle 5 CYP1A2, CYP1B1, CYP2E1, DDX53, LIG4
Microsome membrane 3 CYP1A2, CYP1B1, CYP2E1
postsynaptic density 1 P2RY1
Secreted 4 ACHE, BCHE, F2, VIP
extracellular region 6 ACHE, BCHE, ELANE, F2, MAPK14, VIP
Extracellular side 1 ACHE
ciliary membrane 1 DRD2
dendritic spine 1 DRD2
perikaryon 1 DRD2
Z disc 1 FBXO32
nucleolus 1 DDX53
postsynaptic membrane 2 DRD2, P2RY1
presynaptic active zone membrane 1 P2RY1
Apical cell membrane 1 ABCB1
Mitochondrion inner membrane 1 CYP2E1
GABA-ergic synapse 1 DRD2
Peroxisome 1 XDH
basement membrane 1 ACHE
sarcoplasmic reticulum 1 XDH
collagen-containing extracellular matrix 2 ELANE, F2
secretory granule 1 ELANE
lateral plasma membrane 1 DRD2
nuclear speck 1 MAPK14
neuron projection 1 VIP
cilium 2 DRD2, P2RY1
spindle pole 1 MAPK14
chromosome, telomeric region 1 LIG4
blood microparticle 2 BCHE, F2
non-motile cilium 1 DRD2
Lipid-anchor, GPI-anchor 1 ACHE
sperm flagellum 1 DRD2
cell body 1 P2RY1
side of membrane 1 ACHE
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 1 MAPK14
Golgi lumen 1 F2
endoplasmic reticulum lumen 2 BCHE, F2
transcription repressor complex 1 ELANE
axon terminus 1 DRD2
voltage-gated calcium channel complex 1 CACNA1I
specific granule lumen 1 ELANE
endocytic vesicle 1 DRD2
azurophil granule lumen 1 ELANE
nuclear envelope lumen 1 BCHE
synaptic cleft 1 ACHE
external side of apical plasma membrane 1 ABCB1
dopaminergic synapse 1 DRD2
condensed chromosome 1 LIG4
Cytoplasmic vesicle, phagosome 1 ELANE
SCF ubiquitin ligase complex 1 FBXO32
DNA-dependent protein kinase-DNA ligase 4 complex 1 LIG4
nonhomologous end joining complex 1 LIG4
cell body membrane 1 P2RY12
cell projection membrane 1 P2RY12
G protein-coupled receptor complex 1 DRD2
[Isoform H]: Cell membrane 1 ACHE
DNA ligase IV complex 1 LIG4


文献列表

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  • Binjun Yan, Zi-Ao Huang, Noorfatimah Yahaya, David Da Yong Chen. Enantioselective analysis in complex matrices using capillary electrophoresis-mass spectrometry: A case study of the botanical drug Corydalis Rhizoma. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2020 Sep; 1152(?):122216. doi: 10.1016/j.jchromb.2020.122216. [PMID: 32531643]
  • Manead Khin, Nadja B Cech, Joshua J Kellogg, Lindsay K Caesar. Chemical Evaluation of the Effects of Storage Conditions on the Botanical Goldenseal using Marker-based and Metabolomics Approaches. The Yale journal of biology and medicine. 2020 06; 93(2):265-275. doi: . [PMID: 32607087]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Zhong-Min Zhao, Xiao-Fei Shang, Raymond Kobla Lawoe, Ying-Qian Liu, Rui Zhou, Yu Sun, Yin-Fang Yan, Jun-Cai Li, Guan-Zhou Yang, Cheng-Jie Yang. Anti-phytopathogenic activity and the possible mechanisms of action of isoquinoline alkaloid sanguinarine. Pesticide biochemistry and physiology. 2019 Sep; 159(?):51-58. doi: 10.1016/j.pestbp.2019.05.015. [PMID: 31400784]
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  • Bhawani Datt Joshi, Anubha Srivastava, Poonam Tandon, Sudha Jain, A P Ayala. A combined experimental (IR, Raman and UV-Vis) and quantum chemical study of canadine. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2018 Feb; 191(?):249-258. doi: 10.1016/j.saa.2017.10.008. [PMID: 29040931]
  • Dujun Wang, Kai Wang, Danjuan Sui, Zhen Ouyang, Haiyu Xu, Yuan Wei. Effects of tetrahydroberberine and tetrahydropalmatine on hepatic cytochrome P450 expression and their toxicity in mice. Chemico-biological interactions. 2017 Apr; 268(?):47-52. doi: 10.1016/j.cbi.2017.02.019. [PMID: 28257954]
  • Stephanie Galanie, Christina D Smolke. Optimization of yeast-based production of medicinal protoberberine alkaloids. Microbial cell factories. 2015 Sep; 14(?):144. doi: 10.1186/s12934-015-0332-3. [PMID: 26376732]
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  • Ji Won Jung, Yong Sam Kwon, Jin Seok Jeong, Miwon Son, Hee Eun Kang. Pharmacokinetics and brain distribution of tetrahydropalmatine and tetrahydroberberine after oral administration of DA-9701, a new botanical gastroprokinetic agent, in rats. Biological & pharmaceutical bulletin. 2015; 38(2):285-91. doi: 10.1248/bpb.b14-00678. [PMID: 25747988]
  • Jia-jia Yu, Deng-li Cong, Ying Jiang, Yuan Zhou, Yan Wang, Chun-fang Zhao. [Study on alkaloids of Corydalis ochotensis and their antitumor bioactivity]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2014 Oct; 37(10):1795-8. doi: . [PMID: 25895386]
  • Thu-Thuy T Dang, Peter J Facchini. Cloning and characterization of canadine synthase involved in noscapine biosynthesis in opium poppy. FEBS letters. 2014 Jan; 588(1):198-204. doi: 10.1016/j.febslet.2013.11.037. [PMID: 24316226]
  • Hong Liu, Liang Wang, Yan Li, Jiang Liu, Maomao An, Shaolong Zhu, Yongbing Cao, Zhihui Jiang, Mingzhu Zhao, Zhan Cai, Li Dai, Tingjunhong Ni, Wei Liu, Simin Chen, Changqing Wei, Chengxu Zang, Shujuan Tian, Jingyu Yang, Chunfu Wu, Dazhi Zhang, Hua Liu, Yuanying Jiang. Structural optimization of berberine as a synergist to restore antifungal activity of fluconazole against drug-resistant Candida albicans. ChemMedChem. 2014 Jan; 9(1):207-16. doi: 10.1002/cmdc.201300332. [PMID: 24376206]
  • Yinying Zhang, Kuan Shi, Jun Wen, Guorong Fan, Yifeng Chai, Zhanying Hong. Chiral HPLC determination and stereoselective pharmacokinetics of tetrahydroberberine enantiomers in rats. Chirality. 2012 Mar; 24(3):239-44. doi: 10.1002/chir.21988. [PMID: 22271601]
  • Ziming Lu, Wuxing Sun, Xuhong Duan, Zhiyun Yang, Yadong Liu, Pengfei Tu. [Chemical constituents from Corydalis yanhusuo]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2012 Jan; 37(2):235-7. doi: . [PMID: 22737858]
  • Mingyong Zhang, Jian Le, Jun Wen, Yifeng Chai, Guorong Fan, Zhanying Hong. Simultaneous determination of tetrahydropalmatine and tetrahydroberberine in rat urine using dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography. Journal of separation science. 2011 Nov; 34(22):3279-86. doi: 10.1002/jssc.201100588. [PMID: 22028314]
  • Yingchun Zhang, Haiyu Xu, Xiaomeng Chen, Chang Chen, Haijun Wang, Fanyun Meng, Hongjun Yang, Luqi Huang. Simultaneous quantification of 17 constituents from Yuanhu Zhitong tablet using rapid resolution liquid chromatography coupled with a triple quadrupole electrospray tandem mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2011 Nov; 56(3):497-504. doi: 10.1016/j.jpba.2011.06.008. [PMID: 21733652]
  • Tae Ho Lee, Ki Hyun Kim, Sung Ok Lee, Kang Ro Lee, Miwon Son, Mirim Jin. Tetrahydroberberine, an isoquinoline alkaloid isolated from corydalis tuber, enhances gastrointestinal motor function. The Journal of pharmacology and experimental therapeutics. 2011 Sep; 338(3):917-24. doi: 10.1124/jpet.111.182048. [PMID: 21659472]
  • Keivan A Ettefagh, Johnna T Burns, Hiyas A Junio, Glenn W Kaatz, Nadja B Cech. Goldenseal (Hydrastis canadensis L.) extracts synergistically enhance the antibacterial activity of berberine via efflux pump inhibition. Planta medica. 2011 May; 77(8):835-40. doi: 10.1055/s-0030-1250606. [PMID: 21157683]
  • Ki Hyun Kim, Il Kyun Lee, Cheng Jie Piao, Sang Un Choi, Jei Hyun Lee, Yeong Shik Kim, Kang Ro Lee. Benzylisoquinoline alkaloids from the tubers of Corydalis ternata and their cytotoxicity. Bioorganic & medicinal chemistry letters. 2010 Aug; 20(15):4487-90. doi: 10.1016/j.bmcl.2010.06.035. [PMID: 20594848]
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  • C W Lau, X Q Yao, Z Y Chen, W H Ko, Y Huang. Cardiovascular actions of berberine. Cardiovascular drug reviews. 2001; 19(3):234-44. doi: 10.1111/j.1527-3466.2001.tb00068.x. [PMID: 11607041]
  • H Abdel-Haq, M F Cometa, M Palmery, M G Leone, B Silvestrini, L Saso. Relaxant effects of Hydrastis canadensis L. and its major alkaloids on guinea pig isolated trachea. Pharmacology & toxicology. 2000 Nov; 87(5):218-22. doi: 10.1034/j.1600-0773.2000.d01-77.x. [PMID: 11129501]
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  • B Xuan, W Wang, D X Li. Inhibitory effect of tetrahydroberberine on platelet aggregation and thrombosis. Zhongguo yao li xue bao = Acta pharmacologica Sinica. 1994 Mar; 15(2):133-5. doi: . [PMID: 8010106]
  • B Xuan, D X Li, W Wang. [Protective effects of tetrahydroprotoberberines on experimental myocardial infarction in rats]. Zhongguo yao li xue bao = Acta pharmacologica Sinica. 1992 Mar; 13(2):167-71. doi: . [PMID: 1598835]
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