mafenide (BioDeep_00000006423)

 

Secondary id: BioDeep_00001868383

human metabolite blood metabolite Chemicals and Drugs Antibiotics


代谢物信息卡片


Sanofi winthrop brand OF mafenide acetate

化学式: C7H10N2O2S (186.0463)
中文名称: 4-氨基甲基苯磺酰胺
谱图信息: 最多检出来源 Homo sapiens(blood) 100%

分子结构信息

SMILES: C1=CC(=CC=C1CN)S(=O)(=O)N
InChI: InChI=1S/C7H10N2O2S/c8-5-6-1-3-7(4-2-6)12(9,10)11/h1-4H,5,8H2,(H2,9,10,11)

描述信息

D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BA - Sulfonamides
D004791 - Enzyme Inhibitors > D002257 - Carbonic Anhydrase Inhibitors
C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent
D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents

同义名列表

21 个代谢物同义名

Sanofi winthrop brand OF mafenide acetate; 4-(Aminomethyl)benzene-1-sulphonamide; 4-(aminomethyl)benzene-1-sulfonamide; Bertek brand OF mafenide acetate; 4-HOMOsulphanilamide; 4 Homosulfanilamide; 4-Homosulfanilamide; Acetate, mafenide; Mafenide Acetate; Sulfabenzamine; Bensulfamide; Sulphamylon; Sulfamylon; Marfanil; Maphenid; mafenide; Napaltan; Mafylon; emilene; Mafenide; Mafenide



数据库引用编号

17 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)

1 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 9 AOC3, CA1, CA2, CASP3, DHFR, FGF2, G6PD, GSDMD, NLRP3
Peripheral membrane protein 2 ACHE, G6PD
Endosome membrane 1 AMN
Endoplasmic reticulum membrane 1 PON1
Mitochondrion membrane 1 GSDMD
Nucleus 6 ACHE, CA9, CASP3, CENPV, FGF2, NLRP3
cytosol 8 CA1, CA2, CASP3, CENPV, DHFR, G6PD, GSDMD, NLRP3
mitochondrial membrane 1 GSDMD
nucleoplasm 3 CASP3, CENPV, GSDMD
Cell membrane 7 ACHE, AMN, AOC3, CA12, CA2, CA9, GSDMD
Multi-pass membrane protein 1 GSDMD
Golgi apparatus membrane 1 NLRP3
Synapse 1 ACHE
cell surface 4 ACHE, AOC3, PLG, SERPINF2
glutamatergic synapse 2 CASP3, PLG
Golgi apparatus 2 ACHE, AOC3
Golgi membrane 2 INS, NLRP3
lysosomal membrane 1 EGF
neuromuscular junction 1 ACHE
neuronal cell body 1 CASP3
Cytoplasm, cytosol 2 G6PD, NLRP3
plasma membrane 9 ACHE, AMN, AOC3, CA12, CA2, CA9, EGF, GSDMD, PLG
Membrane 9 ACHE, AMN, AOC3, CA12, CA9, EGF, G6PD, GSDMD, NLRP3
apical plasma membrane 2 AMN, CA12
basolateral plasma membrane 2 CA12, CA9
extracellular exosome 8 AMN, CA1, CA2, EGF, G6PD, PLG, PON1, SERPINF2
endoplasmic reticulum 2 AOC3, NLRP3
extracellular space 9 ACHE, AMN, EGF, FGF2, GSDMD, INS, PLG, PON1, SERPINF2
perinuclear region of cytoplasm 1 ACHE
Schaffer collateral - CA1 synapse 1 PLG
mitochondrion 2 DHFR, NLRP3
intracellular membrane-bounded organelle 1 G6PD
postsynaptic density 1 CASP3
Single-pass type I membrane protein 2 AMN, CA9
Secreted 6 ACHE, FGF2, GSDMD, INS, NLRP3, PLG
extracellular region 10 ACHE, DNAH9, EGF, FGF2, GSDMD, INS, NLRP3, PLG, PON1, SERPINF2
cytoplasmic side of plasma membrane 1 G6PD
Extracellular side 1 ACHE
centriolar satellite 1 G6PD
motile cilium 1 DNAH9
nuclear membrane 1 CENPV
external side of plasma membrane 1 PLG
high-density lipoprotein particle 1 PON1
microtubule cytoskeleton 1 CENPV
nucleolus 1 CA9
midbody 1 CENPV
Early endosome 1 AOC3
apical part of cell 1 CA2
clathrin-coated pit 1 AMN
spindle midzone 1 CENPV
Single-pass type II membrane protein 1 AOC3
Cytoplasm, cytoskeleton, spindle 1 CENPV
microtubule 1 DNAH9
basement membrane 1 ACHE
collagen-containing extracellular matrix 2 PLG, SERPINF2
axoneme 1 DNAH9
Cytoplasm, cytoskeleton, microtubule organizing center 1 NLRP3
Inflammasome 2 GSDMD, NLRP3
interphase microtubule organizing center 1 NLRP3
NLRP3 inflammasome complex 2 GSDMD, NLRP3
receptor complex 1 AMN
brush border membrane 1 AMN
Nucleus, nucleolus 1 CA9
blood microparticle 3 PLG, PON1, SERPINF2
Cytoplasm, cytoskeleton, cilium axoneme 1 DNAH9
Lipid-anchor, GPI-anchor 1 ACHE
Cell projection, microvillus membrane 1 CA9
microvillus membrane 2 AMN, CA9
Endomembrane system 2 GSDMD, NLRP3
endosome lumen 1 INS
microvillus 1 AOC3
Chromosome, centromere, kinetochore 1 CENPV
microtubule organizing center 1 NLRP3
side of membrane 1 ACHE
myelin sheath 1 CA2
ficolin-1-rich granule lumen 1 GSDMD
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 1 INS
platelet alpha granule lumen 3 EGF, PLG, SERPINF2
specific granule lumen 1 GSDMD
tertiary granule lumen 1 GSDMD
kinetochore 1 CENPV
endocytic vesicle 1 AMN
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
9+2 motile cilium 1 DNAH9
dynein complex 1 DNAH9
clathrin-coated endocytic vesicle membrane 1 EGF
synaptic cleft 1 ACHE
death-inducing signaling complex 1 CASP3
Membrane, coated pit 1 AMN
spherical high-density lipoprotein particle 1 PON1
fibrinogen complex 1 SERPINF2
[Isoform H]: Cell membrane 1 ACHE
[Gasdermin-D]: Cytoplasm, cytosol 1 GSDMD
[Gasdermin-D, N-terminal]: Cell membrane 1 GSDMD
[Gasdermin-D, N-terminal]: Cytoplasm, cytosol 1 GSDMD
[Gasdermin-D, p13]: Nucleus 1 GSDMD
[Gasdermin-D, C-terminal]: Cytoplasm, cytosol 1 GSDMD
[Isoform 1]: Apical cell membrane 1 AMN
outer dynein arm 1 DNAH9
[Soluble protein amnionless]: Secreted 1 AMN
distal portion of axoneme 1 DNAH9


文献列表

  • Ramazan Demirdağ, Veysel Çomaklı, Murat Şentürk, Deniz Ekinci, Ö İrfan Küfrevioğlu, Claudiu T Supuran. Purification and characterization of carbonic anhydrase from sheep kidney and effects of sulfonamides on enzyme activity. Bioorganic & medicinal chemistry. 2013 Mar; 21(6):1522-5. doi: 10.1016/j.bmc.2012.08.018. [PMID: 22974493]
  • Rachel A Pendleton, James H Holmes. Systemic absorption of amphotericin B with topical 5\% mafenide acetate/amphotericin B solution for grafted burn wounds: is it clinically relevant?. Burns : journal of the International Society for Burn Injuries. 2010 Feb; 36(1):38-41. doi: 10.1016/j.burns.2009.04.009. [PMID: 19481350]
  • Rajeev B Ahuja, Amit Gupta, Renu Gur. A prospective double-blinded comparative analysis of framycetin and silver sulphadiazine as topical agents for burns: a pilot study. Burns : journal of the International Society for Burn Injuries. 2009 Aug; 35(5):672-6. doi: 10.1016/j.burns.2008.08.015. [PMID: 19443125]
  • Mika Hilvo, Anna Maria Salzano, Alessio Innocenti, Markku S Kulomaa, Andrea Scozzafava, Andrea Scaloni, Seppo Parkkila, Claudiu T Supuran. Cloning, expression, post-translational modifications and inhibition studies on the latest mammalian carbonic anhydrase isoform, CA XV. Journal of medicinal chemistry. 2009 Feb; 52(3):646-54. doi: 10.1021/jm801267c. [PMID: 19193158]
  • Jonna M Lehtonen, Seppo Parkkila, Daniela Vullo, Angela Casini, Andrea Scozzafava, Claudiu T Supuran. Carbonic anhydrase inhibitors. Inhibition of cytosolic isozyme XIII with aromatic and heterocyclic sulfonamides: a novel target for the drug design. Bioorganic & medicinal chemistry letters. 2004 Jul; 14(14):3757-62. doi: 10.1016/j.bmcl.2004.04.106. [PMID: 15203157]
  • A Scozzafava, F Briganti, M A Ilies, C T Supuran. Carbonic anhydrase inhibitors: synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes. Journal of medicinal chemistry. 2000 Jan; 43(2):292-300. doi: 10.1021/jm990479+. [PMID: 10649985]
  • A Scozzafava, F Briganti, G Mincione, L Menabuoni, F Mincione, C T Supuran. Carbonic anhydrase inhibitors: synthesis of water-soluble, aminoacyl/dipeptidyl sulfonamides possessing long-lasting intraocular pressure-lowering properties via the topical route. Journal of medicinal chemistry. 1999 Sep; 42(18):3690-700. doi: 10.1021/jm9901879. [PMID: 10479300]
  • A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione, C T Supuran. Carbonic anhydrase inhibitors. Synthesis of water-soluble, topically effective, intraocular pressure-lowering aromatic/heterocyclic sulfonamides containing cationic or anionic moieties: is the tail more important than the ring?. Journal of medicinal chemistry. 1999 Jul; 42(14):2641-50. doi: 10.1021/jm9900523. [PMID: 10411484]
  • G L Klein, D N Herndon, T C Rutan, J R Barnett, N L Miller, A C Alfrey. Risk of aluminum accumulation in patients with burns and ways to reduce it. The Journal of burn care & rehabilitation. 1994 Jul; 15(4):354-8. doi: 10.1097/00004630-199407000-00011. [PMID: 7929518]
  • R L McCauley, Y Y Li, B Poole, M J Evans, M C Robson, J P Heggers, D N Herndon. Differential inhibition of human basal keratinocyte growth to silver sulfadiazine and mafenide acetate. The Journal of surgical research. 1992 Mar; 52(3):276-85. doi: 10.1016/0022-4804(92)90086-f. [PMID: 1538606]
  • M L Cooper, S T Boyce, J F Hansbrough, T J Foreman, D H Frank. Cytotoxicity to cultured human keratinocytes of topical antimicrobial agents. The Journal of surgical research. 1990 Mar; 48(3):190-5. doi: 10.1016/0022-4804(90)90212-k. [PMID: 2314091]
  • D J Weisdorf, J H Aldridge. Mafenide (Sulfamylon) inhibits plasmin fibrinolytic activity. Thrombosis and haemostasis. 1988 Jun; 59(3):440-4. doi: . [PMID: 2973151]
  • P R Liebman, M M Kennelly, E F Hirsch. Hypercarbia and acidosis associated with carbonic anhydrase inhibition: a hazard of topical mafenide acetate use in renal failure. Burns, including thermal injury. 1982 Jul; 8(6):395-8. doi: 10.1016/0305-4179(82)90109-7. [PMID: 6809230]
  • G Erbs, F E Müller, W Opferkuch. [The effect of burns on the complement system]. Fortschritte der Medizin. 1980 Mar; 98(11):397-9. doi: NULL. [PMID: 6154634]
  • J M Steyn. Thin-layer chromatographic determination of mafenide [(p-aminomethyl) benzenesulphonamide] in human serum. Journal of chromatography. 1977 Mar; 143(2):210-3. doi: 10.1016/s0378-4347(00)81827-7. [PMID: 838834]
  • W L Brown, E G Bowler, A D Mason, B A pruitt. Protein metabolism in burned rats. The American journal of physiology. 1976 Aug; 231(2):476-82. doi: 10.1152/ajplegacy.1976.231.2.476. [PMID: 961900]
  • G STUTTGEN. [Marfanil in the serum following peroral administration]. Naunyn-Schmiedebergs Archiv fur experimentelle Pathologie und Pharmakologie. 1950; 210(4-5):431-6. doi: NULL. [PMID: 14777503]
  • R C RUTLEDGE, W G KLINGBERG, M L HEIDEMAN. Nephrocalcinosis and Pseudomonas aeruginosa pyelonephritis; treatment with p-aminomethylbenzene-sulfonamide (sulfamylon). The Journal of pediatrics. 1949 Jul; 35(1):88-93. doi: 10.1016/s0022-3476(49)80036-9. [PMID: 18132990]