Ehotiophat

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Ehotiophat
Klinički podaci
Prodajno imeEchodide, Phospholine Iodide
Drugs.comMonografija
Način primeneOftalmički
Identifikatori
CAS broj6736-03-4 ДаY
ATC kodNone
PubChemCID 10547
DrugBankDB01057 ДаY
ChemSpider10107 ДаY
ChEBICHEBI:4753 ДаY
ChEMBLCHEMBL1201341 ДаY
Hemijski podaci
FormulaC9H23NO3PS
Molarna masa256,323
  • CCOP(=O)(OCC)SCC[N+](C)(C)C
  • InChI=1S/C9H23NO3PS/c1-6-12-14(11,13-7-2)15-9-8-10(3,4)5/h6-9H2,1-5H3/q+1 ДаY
  • Key:BJOLKYGKSZKIGU-UHFFFAOYSA-N ДаY
Fizički podaci
Tačka topljenja138 °C (280 °F)

Ehotiophat je organsko jedinjenje, koje sadrži 9 atoma ugljenika i ima molekulsku masu od 256,323 Da.[1][2][3][4]

Osobine[uredi | uredi izvor]

Osobina Vrednost
Broj akceptora vodonika 4
Broj donora vodonika 0
Broj rotacionih veza 8
Particioni koeficijent[5] (ALogP) -0,1
Rastvorljivost[6] (logS, log(mol/L)) -2,5
Polarna površina[7] (PSA, Å2) 70,6

Reference[uredi | uredi izvor]

  1. ^ Schmidt KG, Horowitz Y, Buckman G, Segev E, Levinger E, Geyer O: Lowering of IOP by echothiophate iodide in pseudophakic eyes with glaucoma. Curr Eye Res. 2010 Aug;35(8):698-702. PMID 20673046 20673046
  2. ^ Reddy RH: Echothiophate iodide: its use in accommodative esotropia (high Ac/A ratio). Indian J Ophthalmol. 1982 Jul;30(4):225. PMID 7166393
  3. ^ Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035—41. PMC 3013709Слободан приступ. PMID 21059682. doi:10.1093/nar/gkq1126. 
  4. ^ David S. Wishart; Craig Knox; An Chi Guo; Dean Cheng; Savita Shrivastava; Dan Tzur; Bijaya Gautam; Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic acids research. 36 (Database issue): D901—6. PMC 2238889Слободан приступ. PMID 18048412. doi:10.1093/nar/gkm958. 
  5. ^ Ghose, A.K.; Viswanadhan V.N. & Wendoloski, J.J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragment Methods: An Analysis of AlogP and CLogP Methods”. J. Phys. Chem. A. 102: 3762—3772. doi:10.1021/jp980230o. 
  6. ^ Tetko IV, Tanchuk VY, Kasheva TN, Villa AE (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Chem Inf. Comput. Sci. 41: 1488—1493. PMID 11749573. doi:10.1021/ci000392t. 
  7. ^ Ertl P.; Rohde B.; Selzer P. (2000). „Fast calculation of molecular polar surface area as a sum of fragment based contributions and its application to the prediction of drug transport properties”. J. Med. Chem. 43: 3714—3717. PMID 11020286. doi:10.1021/jm000942e. 

Literatura[uredi | uredi izvor]

Spoljašnje veze[uredi | uredi izvor]