Linkomicin

Linkomicin
Klinički podaci


Prodajno ime	Lincocin, Lincocine, Lincolcina, Lincolnensin
Drugs.com	Monografija
Način primene	Intravenozno
Farmakokinetički podaci
Poluvreme eliminacije	5,4 ± 1,0 h
Izlučivanje	Renalno

Identifikatori
CAS broj	154-21-2^Y
ATC kod	J01FF02 (WHO)
PubChem	CID 656509
DrugBank	DB01627^Y
ChemSpider	570892^Y
KEGG	C06812^Y
ChEBI	CHEBI:6472^Y
ChEMBL	CHEMBL1447^Y
Hemijski podaci
Formula	C₁₈H₃₄N₂O₆S
Molarna masa	406,537
SMILES [H][C@@]1(O[C@]([H])([C@H](NC(=O)C2C[C@@H](CCC)CN2C)[C@@H](C)O)[C@H](O)[C@H](O)[C@H]1O)SC
InChI InChI=1S/C18H34N2O6S/c1-5-6-10-7-11(20(3)8-10)17(25)19-12(9(2)21)16-14(23)13(22)15(24)18(26-16)27-4/h9-16,18,21-24H,5-8H2,1-4H3,(H,19,25)/t9-,10-,11?,12-,13+,14-,15-,16-,18-/m1/s1^Y Key:OJMMVQQUTAEWLP-ISVUEQNNSA-N^Y

Linkomicin je organsko jedinjenje, koje sadrži 18 atoma ugljenika i ima molekulsku masu od 406,537 Da.^[1]^[2]

Osobine

Osobina	Vrednost
Broj akceptora vodonika	8
Broj donora vodonika	5
Broj rotacionih veza	7
Particioni koeficijent^[3] (ALogP)	0,1
Rastvorljivost^[4] (logS, log(mol/L))	-2,3
Polarna površina^[5] (PSA, Å²)	147,8

^ 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 3013709 . PMID 21059682. doi:10.1093/nar/gkq1126.
^ 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 2238889 . PMID 18048412. doi:10.1093/nar/gkm958.
^ 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.
^ 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.
^ 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.

Hardman JG, Limbird LE, Gilman AG (2001). Goodman & Gilman's The Pharmacological Basis of Therapeutics (10. изд.). New York: McGraw-Hill. ISBN 0071354697. doi:10.1036/0071422803.
Thomas L. Lemke; David A. Williams, ур. (2007). Foye's Principles of Medicinal Chemistry (6. изд.). Baltimore: Lippincott Willams & Wilkins. ISBN 0781768799.

Streptomyces	Streptomicin Neomicin (Framicetin, Paromomicin, Ribostamicin) Kanamicin (Amikacin, Arbekacin, Bekanamicin, Dibekacin, Tobramicin) Spektinomicin^# • Higromicin B Paromomicin
Micromonospora	Gentamicin^# (Netilmicin, Sisomicin, Isepamicin) Verdamicin Astromicin

Tetraciklini	Doksiciklin^# •Hlortetraciklin • Klomociklin • Demeklociklin • Limeciklin • Meklociklin • Metaciklin • Minociklin • Oksitetraciklin • Penimepiciklin • Rolitetraciklin • Tetraciklin
Glicilciklini	Tigeciklin

Amfenikoli	Hloramfenikol^# • Azidamfenikol • Tiamfenikol • Florfenikol
Pleuromutilini	Retapamulin • Tiamulin • Valnemulin

Makrolidi	Eritromicin^# • Azitromicin^# • Spiramicin • Midekamicin • Oleandomicin • Roksitromicin • Jozamicin • Troleandomicin • Klaritromicin • Miokamicin • Rokitamicin • Diritromicin • Fluritromicin • Ketolid (Telitromicin, Cetromicin)
Linkozamidi	Klindamicin^# • Linkomicin
Streptogramini	Pristinamicin • Hinupristin/dalfopristin • Virginijamicin