Fuzidinska kiselina

Fuzidinska kiselina
Klinički podaci

Prodajno ime	Fucidin, Fucidin acid, Fucidin Cream 2%, Fucidine
Drugs.com	acid.html Monografija
Farmakokinetički podaci
Poluvreme eliminacije	5 - 6 h

Identifikatori
CAS broj	6990-06-3^Y
ATC kod	D09AA02 (WHO), J01XC01
PubChem	CID 3000226
DrugBank	DB02703^Y
ChemSpider	2271900^Y
KEGG	C06694^Y
ChEBI	CHEBI:29013^Y
ChEMBL	CHEMBL374975^Y
Hemijski podaci
Formula	C₃₁H₄₈O₆
Molarna masa	516,709
SMILES O[C@@H]1CC[C@@]2(C)[C@@]([H])(CC[C@@]3(C)[C@@]2([H])[C@H](O)C[C@@]2([H])\C([C@@H](OC(=O)C)C[C@]32C)=C(/CCC=C(C)C)C(O)=O)[C@@H]1C
InChI InChI=1S/C31H48O6/c1-17(2)9-8-10-20(28(35)36)26-22-15-24(34)27-29(5)13-12-23(33)18(3)21(29)11-14-30(27,6)31(22,7)16-25(26)37-19(4)32/h9,18,21-25,27,33-34H,8,10-16H2,1-7H3,(H,35,36)/b26-20-/t18-,21-,22-,23+,24+,25-,27-,29-,30-,31-/m0/s1^Y Key:IECPWNUMDGFDKC-MZJAQBGESA-N^Y

Fizički podaci
Tačka topljenja	1.925 °C (3.497 °F)

Fuzidinska kiselina je organsko jedinjenje, koje sadrži 31 atom ugljenika i ima molekulsku masu od 516,709 Da.^[1]^[2]

Osobine

Osobina	Vrednost
Broj akceptora vodonika	6
Broj donora vodonika	3
Broj rotacionih veza	6
Particioni koeficijent^[3] (ALogP)	5,1
Rastvorljivost^[4] (logS, log(mol/L))	-7,0
Polarna površina^[5] (PSA, Å²)	104,1

^ 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