A α C (BioDeep_00000409808)

Main id: BioDeep_00000003643

 


代谢物信息卡片


2-Amino-9H-pyrido[2,3-b]indole (AalphaC)

化学式: C11H9N3 (183.0796)
中文名称: 2-氨基-9H-吡啶鎓[2-3-b] 吲哚
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C(=C1)C3=C(N2)N=C(C=C3)N
InChI: InChI=1S/C11H9N3/c12-10-6-5-8-7-3-1-2-4-9(7)13-11(8)14-10/h1-6H,(H3,12,13,14)

描述信息

CONFIDENCE standard compound; INTERNAL_ID 2443

同义名列表

4 个代谢物同义名

2-Amino-9H-pyrido[2,3-b]indole; A α C; 2-Amino-9H-pyrido[2,3-b]indole (AalphaC); 2-Amino-9H-pyrido[2,3-b]indole



数据库引用编号

14 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(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)

0 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 12 AHR, ALB, APC, APOE, AR, CYP1A1, ESR1, HPGDS, NAT2, NOTCH2, PDCL, SULT1A1
Peripheral membrane protein 3 CYP1A1, CYP1B1, ESR1
Endoplasmic reticulum membrane 7 CYP1A1, CYP1A2, CYP1B1, NOTCH2, UGT1A1, UGT1A4, UGT1A9
Nucleus 8 AHR, ALB, APC, APOE, AR, ESR1, NAT2, NOTCH2
cytosol 11 AHR, ALB, APC, AR, CD28, ESR1, HPGDS, NAT1, NAT2, PDCL, SULT1A1
dendrite 1 APOE
centrosome 2 ALB, APC
nucleoplasm 6 AHR, APC, AR, ESR1, HPGDS, NOTCH2
Cell membrane 5 APC, CD28, ESR1, NAT1, NAT2
Cytoplasmic side 1 ESR1
lamellipodium 1 APC
ruffle membrane 1 APC
Multi-pass membrane protein 3 NAT1, NAT2, SLC45A2
Synapse 1 NAT1
cell surface 3 CD28, NAT1, NOTCH2
glutamatergic synapse 1 APOE
Golgi apparatus 4 ALB, APC, APOE, ESR1
Golgi membrane 1 NOTCH2
mitochondrial inner membrane 1 CYP1A1
neuronal cell body 2 APOE, NAT2
presynaptic membrane 1 NAT1
plasma membrane 9 APC, APOE, AR, CD28, ESR1, NAT1, NAT2, NOTCH2, UGT1A1
synaptic vesicle membrane 1 NAT1
Membrane 11 APOE, AR, CYP1B1, ESR1, NAT1, NAT2, NOTCH2, SLC45A2, UGT1A1, UGT1A4, UGT1A9
apical plasma membrane 1 NAT1
axon 2 NAT1, NAT2
basolateral plasma membrane 2 NAT1, NAT2
extracellular exosome 3 ALB, APOE, NAT2
endoplasmic reticulum 5 ALB, APOE, UGT1A1, UGT1A4, UGT1A9
extracellular space 2 ALB, APOE
perinuclear region of cytoplasm 2 APC, UGT1A1
adherens junction 1 APC
bicellular tight junction 1 APC
mitochondrion 2 CYP1A1, CYP1B1
protein-containing complex 4 AHR, ALB, AR, ESR1
intracellular membrane-bounded organelle 4 CYP1A1, CYP1A2, CYP1B1, HPGDS
Microsome membrane 3 CYP1A1, CYP1A2, CYP1B1
Single-pass type I membrane protein 1 NOTCH2
Secreted 2 ALB, APOE
extracellular region 3 ALB, APOE, NOTCH2
Single-pass membrane protein 3 UGT1A1, UGT1A4, UGT1A9
neuronal cell body membrane 1 NAT1
anchoring junction 1 ALB
transcription regulator complex 3 AHR, ESR1, NAT2
Cell projection, cilium 1 PDCL
external side of plasma membrane 1 CD28
Endosome, multivesicular body 1 APOE
Extracellular vesicle 1 APOE
Secreted, extracellular space, extracellular matrix 1 APOE
chylomicron 1 APOE
high-density lipoprotein particle 1 APOE
low-density lipoprotein particle 1 APOE
multivesicular body 1 APOE
very-low-density lipoprotein particle 1 APOE
beta-catenin destruction complex 1 APC
Wnt signalosome 1 APC
Melanosome membrane 1 SLC45A2
Early endosome 1 APOE
Cell projection, lamellipodium 1 APC
Cell projection, ruffle membrane 1 APC
Cytoplasm, perinuclear region 1 UGT1A1
Mitochondrion inner membrane 1 CYP1A1
Cytoplasm, cytoskeleton 1 APC
microtubule 1 APC
Cell junction, adherens junction 1 APC
extracellular matrix 1 APOE
collagen-containing extracellular matrix 1 APOE
lateral plasma membrane 1 APC
nuclear speck 1 AR
receptor complex 1 NOTCH2
ciliary basal body 1 ALB
cilium 2 NOTCH2, PDCL
chromatin 3 AHR, AR, ESR1
cell periphery 1 APC
centriole 1 ALB
Secreted, extracellular space 1 APOE
spindle pole 1 ALB
blood microparticle 2 ALB, APOE
Basolateral cell membrane 1 NAT1
aryl hydrocarbon receptor complex 1 AHR
Melanosome 1 APOE
euchromatin 1 ESR1
endoplasmic reticulum lumen 2 ALB, APOE
platelet alpha granule lumen 1 ALB
kinetochore 1 APC
immunological synapse 1 CD28
clathrin-coated endocytic vesicle membrane 1 APOE
[Isoform 1]: Nucleus 1 ESR1
synaptic cleft 1 APOE
external side of apical plasma membrane 1 NAT2
catenin complex 1 APC
discoidal high-density lipoprotein particle 1 APOE
endocytic vesicle lumen 1 APOE
chylomicron remnant 1 APOE
intermediate-density lipoprotein particle 1 APOE
lipoprotein particle 1 APOE
multivesicular body, internal vesicle 1 APOE
endoplasmic reticulum chaperone complex 1 UGT1A1
[Isoform 3]: Cell surface 1 CD28
protein complex involved in cell adhesion 1 CD28
cytochrome complex 1 UGT1A1
nuclear aryl hydrocarbon receptor complex 1 AHR
cytosolic aryl hydrocarbon receptor complex 1 AHR
NatA complex 1 NAT2
ciliary transition fiber 1 ALB
[Notch 2 extracellular truncation]: Cell membrane 1 NOTCH2
[Notch 2 intracellular domain]: Nucleus 1 NOTCH2


文献列表

  • Li Zhang, Lanqing Wang, Yao Li, Yang Xia, Cindy M Chang, Baoyun Xia, Connie S Sosnoff, Brittany N Pine, B Rey deCastro, Benjamin C Blount. Evaluation of Tobacco Smoke and Diet as Sources of Exposure to Two Heterocyclic Aromatic Amines for the U.S. Population: NHANES 2013-2014. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2020 01; 29(1):103-111. doi: 10.1158/1055-9965.epi-19-0169. [PMID: 31575556]
  • Falco Beer, Felix Urbat, Charles M A P Franz, Melanie Huch, Sabine E Kulling, Mirko Bunzel, Diana Bunzel. The Human Fecal Microbiota Metabolizes Foodborne Heterocyclic Aromatic Amines by Reuterin Conjugation and Further Transformations. Molecular nutrition & food research. 2019 05; 63(10):e1801177. doi: 10.1002/mnfr.201801177. [PMID: 30815965]
  • Ram B Jain. Concentrations of selected heterocyclic aromatic amines among US population aged ≥ 6 years: data from NHANES 2013-2014. Environmental science and pollution research international. 2018 Jul; 25(20):19859-19874. doi: 10.1007/s11356-018-2210-0. [PMID: 29737487]
  • Katia Sayyed, Marc Le Vee, Ziad Abdel-Razzak, Olivier Fardel. Inhibition of organic anion transporter (OAT) activity by cigarette smoke condensate. Toxicology in vitro : an international journal published in association with BIBRA. 2017 Oct; 44(?):27-35. doi: 10.1016/j.tiv.2017.06.014. [PMID: 28629854]
  • Kai Hu, Ge Zhao, Yufeng Fu, Sheng Wang, Hang Yuan, Fuwei Xie, Shusheng Zhang, Huimin Liu, Minying Liu. Screening and identification of the main metabolites of 2-amino-9H-pyrido[2,3-b]indole (AαC) in liver microsomes and rat urine by using UPLC-Q-TOF-MS/MS. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2017 Mar; 1046(?):110-121. doi: 10.1016/j.jchromb.2017.01.038. [PMID: 28157663]
  • Robert J Turesky, Dmitri Konorev, Xiaoyu Fan, Yijin Tang, Lihua Yao, Xinxin Ding, Fang Xie, Yi Zhu, Qing-Yu Zhang. Effect of Cytochrome P450 Reductase Deficiency on 2-Amino-9H-pyrido[2,3-b]indole Metabolism and DNA Adduct Formation in Liver and Extrahepatic Tissues of Mice. Chemical research in toxicology. 2015 Dec; 28(12):2400-10. doi: 10.1021/acs.chemrestox.5b00405. [PMID: 26583703]
  • Khyatiben V Pathak, Medjda Bellamri, Yi Wang, Sophie Langouët, Robert J Turesky. 2-Amino-9H-pyrido[2,3-b]indole (AαC) Adducts and Thiol Oxidation of Serum Albumin as Potential Biomarkers of Tobacco Smoke. The Journal of biological chemistry. 2015 Jun; 290(26):16304-18. doi: 10.1074/jbc.m115.646539. [PMID: 25953894]
  • Fernando De Andrés, Mohammed Zougagh, Gregorio Castañeda, José Luis Sánchez-Rojas, Angel Ríos. Screening of non-polar heterocyclic amines in urine by microextraction in packed sorbent-fluorimetric detection and confirmation by capillary liquid chromatography. Talanta. 2011 Feb; 83(5):1562-7. doi: 10.1016/j.talanta.2010.11.060. [PMID: 21238752]
  • Carlos Lopez-Mendez, Alexandra Bermudez-Fajardo, Costas Ioannides, Ernesto Oviedo-Orta. Effect of 2-amino-9H-pyrido[2,3-b]indole (AalphaC), a carcinogenic heterocyclic amine present in food, on atherosclerotic plaque development in apoE deficient mice. Toxicology letters. 2009 Mar; 185(2):73-8. doi: 10.1016/j.toxlet.2008.11.014. [PMID: 19103270]
  • Carola Funk, Annett Braune, John H Grabber, Hans Steinhart, Mirko Bunzel. Model studies of lignified fiber fermentation by human fecal microbiota and its impact on heterocyclic aromatic amine adsorption. Mutation research. 2007 Nov; 624(1-2):41-8. doi: 10.1016/j.mrfmmm.2007.03.010. [PMID: 17475287]
  • Robert J Turesky, Jian-Min Yuan, Renwei Wang, Sabrina Peterson, Mimi C Yu. Tobacco smoking and urinary levels of 2-amino-9H-pyrido[2,3-b]indole in men of Shanghai, China. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2007 Aug; 16(8):1554-60. doi: 10.1158/1055-9965.epi-07-0132. [PMID: 17684128]
  • Zhi-Xin Yuan, Gautam Jha, Michael A McGregor, Roberta S King. Metabolites of the carcinogen 2-amino-alpha-carboline formed in male Sprague-Dawley rats in vivo and in rat hepatocyte and human HepG2 cell incubates. Chemical research in toxicology. 2007 Mar; 20(3):497-503. doi: 10.1021/tx600303d. [PMID: 17291013]
  • Hanne Frederiksen, Henrik Frandsen, Wolfgang Pfau. Syntheses of DNA adducts of two heterocyclic amines, 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeAalphaC) and 2-amino-9H-pyrido[2,3-b]indole (AalphaC) and identification of DNA adducts in organs from rats dosed with MeAalphaC. Carcinogenesis. 2004 Aug; 25(8):1525-33. doi: 10.1093/carcin/bgh156. [PMID: 15059926]
  • Ricky D Holland, Jason Taylor, Laura Schoenbachler, Richard C Jones, James P Freeman, Dwight W Miller, Brian G Lake, Nigel J Gooderham, Robert J Turesky. Rapid biomonitoring of heterocyclic aromatic amines in human urine by tandem solvent solid phase extraction liquid chromatography electrospray ionization mass spectrometry. Chemical research in toxicology. 2004 Aug; 17(8):1121-36. doi: 10.1021/tx049910a. [PMID: 15310244]
  • H Frederiksen, H Frandsen. Excretion of metabolites in urine and faeces from rats dosed with the heterocyclic amine, 2-amino-9H-pyrido[2,3-b]indole (AalphaC). Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2004 Jun; 42(6):879-85. doi: 10.1016/j.fct.2004.01.011. [PMID: 15110096]
  • P Baranczewski, J A Gustafsson, L Moller. DNA adduct formation of 14 heterocyclic aromatic amines in mouse tissue after oral administration and characterization of the DNA adduct formed by 2-amino-9H-pyrido[2,3-b]indole (AalphaC), analysed by 32P_HPLC. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals. 2004 May; 9(3):243-57. doi: 10.1080/13547500400010056. [PMID: 15764290]
  • Markus Zsivkovits, Kassie Fekadu, Gerhard Sontag, Ursula Nabinger, Wolfgang W Huber, Michael Kundi, Asima Chakraborty, Helmuth Foissy, Siegfried Knasmüller. Prevention of heterocyclic amine-induced DNA damage in colon and liver of rats by different lactobacillus strains. Carcinogenesis. 2003 Dec; 24(12):1913-8. doi: 10.1093/carcin/bgg167. [PMID: 12970070]
  • H Horie, M Zeisig, K Hirayama, T Midtvedt, L Möller, J Rafter. Probiotic mixture decreases DNA adduct formation in colonic epithelium induced by the food mutagen 2-amino-9H-pyrido[2,3-b]indole in a human-flora associated mouse model. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP). 2003 Apr; 12(2):101-7. doi: 10.1097/00008469-200304000-00003. [PMID: 12671533]
  • Yaowarate Intiyot, Takemi Kinouchi, Keiko Kataoka, Hideki Arimochi, Tomomi Kuwahara, Usanee Vinitketkumnuen, Yoshinari Ohnishi. Antimutagenicity of Murdannia loriformis in the Salmonella mutation assay and its inhibitory effects on azoxymethane-induced DNA methylation and aberrant crypt focus formation in male F344 rats. The journal of medical investigation : JMI. 2002 Feb; 49(1-2):25-34. doi: ". [PMID: 11901756]
  • K Hirayama, P Baranczewski, J E Akerlund, T Midtvedt, L Möller, J Rafter. Effects of human intestinal flora on mutagenicity of and DNA adduct formation from food and environmental mutagens. Carcinogenesis. 2000 Nov; 21(11):2105-11. doi: 10.1093/carcin/21.11.2105. [PMID: 11062175]
  • E G Snyderwine, N Sadrieh, R S King, H A Schut. Formation of DNA adducts of the food-derived mutagen 2-amino-9H-pyrido-[2,3-b]indole (A(alpha)C) and bioassay of mammary gland carcinogenicity in Sprague-Dawley rats. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 1998 Dec; 36(12):1033-41. doi: 10.1016/s0278-6915(98)00088-x. [PMID: 9862644]