Aminocandin

Aminocandin
Clinical data
Other names	IP-960, HMR-3270
ATC code	none;
Identifiers
	IUPAC name 1-[4-[(2-aminoethyl)amino]-N2-[(4'-octyloxy)[1,1'-biohenyl]-4-yl]carbonyl]-L-ornithine]-4-[4-(4-hydroxyphenyl)-L-threonine]-5-L-serine-echinocandin B;
CAS Number	227472-48-2 ;
PubChem CID	16072305;
ChemSpider	17231781;
ChEBI	CHEBI:84073 ;
Chemical and physical data
Formula	C56H79N9O13
Molar mass	1086.298 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCCCCCCOc1ccc(cc1)c2ccc(cc2)C(=O)NC3CC(CNC(=O)[C@@H]4[C@H]([C@H](CN4C(=O)[C@H](NC(=O)[C@@H](NC(=O)[C@@H]5C[C@H](CN5C(=O)[C@@H](NC3=O)[C@@H](C)O)O)[C@@H](Cc6ccccc6)O)CO)C)O)NCCN;
	InChI InChI=1S/C56H79N9O13/c1-4-5-6-7-8-12-25-78-41-21-19-37(20-22-41)36-15-17-38(18-16-36)50(71)60-42-27-39(58-24-23-57)29-59-54(75)48-49(70)33(2)30-65(48)55(76)43(32-66)61-53(74)47(45(69)26-35-13-10-9-11-14-35)63-52(73)44-28-40(68)31-64(44)56(77)46(34(3)67)62-51(42)72/h9-11,13-22,33-34,39-40,42-49,58,66-70H,4-8,12,23-32,57H2,1-3H3,(H,59,75)(H,60,71)(H,61,74)(H,62,72)(H,63,73)/t33-,34+,39?,40+,42?,43+,44-,45+,46-,47-,48-,49-/m0/s1; Key:JYBUOENGZWTZGU-JZCGONIASA-N;
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Aminocandin is an echinocandin antifungal. It works by targeting the glucan in fungal cell walls.[1][2]

References

Andes D, Marchillo K, Lowther J, Bryskier A, Stamstad T, Conklin R (April 2003). "In vivo pharmacodynamics of HMR 3270, a glucan synthase inhibitor, in a murine candidiasis model". Antimicrobial Agents and Chemotherapy. 47 (4): 1187–92. doi:10.1128/aac.47.4.1187-1192.2003. PMC 152480. PMID 12654645.
Brzankalski GE, Najvar LK, Wiederhold NP, Bocanegra R, Fothergill AW, Rinaldi MG, et al. (November 2008). "Evaluation of aminocandin and caspofungin against Candida glabrata including isolates with reduced caspofungin susceptibility". The Journal of Antimicrobial Chemotherapy. 62 (5): 1094–100. doi:10.1093/jac/dkn304. PMC 2721694. PMID 18658194.

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