Пређи на садржај

Metdilazin

С Википедије, слободне енциклопедије
Metdilazin
Klinički podaci
Prodajno imeBristaline, Dilosyn, Disyncram, Disyncran
Drugs.comMonografija
Identifikatori
CAS broj1982-37-2 ДаY
ATC kodR06AD04 (WHO)
PubChemCID 14677
DrugBankDB00902 ДаY
ChemSpider14009 ДаY
KEGGC07175 ДаY
ChEMBLCHEMBL1200959 ДаY
Hemijski podaci
FormulaC18H20N2S
Molarna masa296,430
  • CN1CCC(CN2C3=CC=CC=C3SC3=CC=CC=C23)C1
  • InChI=1S/C18H20N2S/c1-19-11-10-14(12-19)13-20-15-6-2-4-8-17(15)21-18-9-5-3-7-16(18)20/h2-9,14H,10-13H2,1H3 ДаY
  • Key:HTMIBDQKFHUPSX-UHFFFAOYSA-N ДаY
Fizički podaci
Tačka topljenja87—88 °C (189—190 °F)

Metdilazin je organsko jedinjenje, koje sadrži 18 atoma ugljenika i ima molekulsku masu od 296,430 Da.[1][2][3][4][5]

Osobina Vrednost
Broj akceptora vodonika 3
Broj donora vodonika 0
Broj rotacionih veza 2
Particioni koeficijent[6] (ALogP) 4,1
Rastvorljivost[7] (logS, log(mol/L)) -3,9
Polarna površina[8] (PSA, Å2) 31,8
  1. ^ Rani Basu L, Mazumdar K, Dutta NK, Karak P, Dastidar SG: Antibacterial property of the antipsychotic agent prochlorperazine, and its synergism with methdilazine. Microbiol Res. 2005;Rani Basu, L.; Mazumdar, K.; Dutta, N. K.; Karak, P.; Dastidar, S. G. (2005). „Antibacterial property of the antipsychotic agent prochlorperazine, and its synergism with methdilazine”. Microbiological Research. 160 (1): 95—100. PMID 15782943. doi:10.1016/j.micres.2004.10.002. 
  2. ^ Chattopadhyay D, Mukherjee T, Pal P, Saha B, Bhadra R (1998 Jul). „Altered membrane permeability as the basis of bactericidal action of methdilazine”. J Antimicrob Chemother. 42 (1): 83—6. PMID 9700532. doi:10.1093/jac/42.1.83.  Проверите вредност парамет(а)ра за датум: |date= (помоћ)
  3. ^ Chattopadhyay D, Dastidar SG, Chakrabarty AN: Antimicrobial properties of methdilazine and its synergism with antibiotics and some chemotherapeutic agents. Arzneimittelforschung. Chattopadhyay, D.; Dastidar, S. G.; Chakrabarty, A. N. (1988 Jul). „Antimicrobial properties of methdilazine and its synergism with antibiotics and some chemotherapeutic agents”. Arzneimittel-Forschung. 38 (7): 869—72. PMID 2905130.  Проверите вредност парамет(а)ра за датум: |date= (помоћ)
  4. ^ 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, A. C.; Wishart, D. S. (2011). „DrugBank 3.0: A comprehensive resource for 'Omics' research on drugs”. Nucleic Acids Research. 39 (Database issue): D1035—D1041. PMC 3013709Слободан приступ. PMID 21059682. doi:10.1093/nar/gkq1126. 
  5. ^ Wishart, David S.; Knox, Craig; Guo, An Chi; Cheng, Dean; Shrivastava, Savita; Tzur, Dan; Gautam, Bijaya; Hassanali, Murtaza (2008). „DrugBank: A knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Research. 36 (Database issue): D901—D906. PMC 2238889Слободан приступ. PMID 18048412. doi:10.1093/nar/gkm958. 
  6. ^ Ghose, Arup K.; Viswanadhan, Vellarkad N.; Wendoloski, John J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragmental Methods: An Analysis of ALOGP and CLOGP Methods”. The Journal of Physical Chemistry A. 102 (21): 3762—3772. Bibcode:1998JPCA..102.3762G. doi:10.1021/jp980230o. 
  7. ^ Tetko, Igor V.; Tanchuk, Vsevolod Yu.; Kasheva, Tamara N.; Villa, Alessandro E. P. (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Journal of Chemical Information and Computer Sciences. 41 (6): 1488—1493. PMID 11749573. doi:10.1021/ci000392t. 
  8. ^ Ertl, Peter; Rohde, Bernhard; Selzer, Paul (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”. Journal of Medicinal Chemistry. 43 (20): 3714—3717. PMID 11020286. doi:10.1021/jm000942e. 

Spoljašnje veze

[уреди | уреди извор]


Molimo Vas, obratite pažnju na važno upozorenje
u vezi sa temama iz oblasti medicine (zdravlja).