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Details

Stereochemistry ABSOLUTE
Molecular Formula C44H80N2O15.2K.2H2O4P
Molecular Weight 1149.2815
Optical Activity UNSPECIFIED
Defined Stereocenters 22 / 22
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEGALOMICIN POTASSIUM PHOSPHATE

SMILES

[K+].[K+].OP(O)([O-])=O.OP(O)([O-])=O.[H][C@@]2(O[C@H]1C[C@@](C)(O)[C@@H](O)[C@H](C)O1)[C@@H](C)C(=O)O[C@H](CC)[C@@](C)(O)[C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O[C@H]3C[C@H]([C@@H](O)[C@H](C)O3)N(C)C)[C@]([H])(O[C@@H]4O[C@H](C)C[C@@H]([C@H]4O)N(C)C)[C@H]2C

InChI

InChIKey=YVWJEFDUJZGAQS-CTMPRURZSA-L
InChI=1S/C44H80N2O15.2K.2H3O4P/c1-16-30-44(11,54)37(50)23(4)33(47)21(2)19-43(10,61-31-18-29(46(14)15)34(48)26(7)56-31)39(60-41-35(49)28(45(12)13)17-22(3)55-41)24(5)36(25(6)40(52)58-30)59-32-20-42(9,53)38(51)27(8)57-32;;;2*1-5(2,3)4/h21-32,34-39,41,48-51,53-54H,16-20H2,1-15H3;;;2*(H3,1,2,3,4)/q;2*+1;;/p-2/t21-,22-,23+,24+,25-,26+,27+,28+,29-,30-,31+,32+,34+,35-,36+,37-,38+,39-,41+,42-,43-,44-;;;;/m1..../s1

HIDE SMILES / InChI
Megalomicin is a Micromonospora-produced macrolide antibiotic complex. Megalomicin A component was studied most extensively. It inhibited the ATP-dependent acidification of lysosomes and intra-Golgi transport in vitro. Megalomicin induces a powerful inhibitory effect on HIV-1 replication at nontoxic concentrations by preventing the processing of HIV-1 gp160 envelope protein and the subsequent formation of infectious viral particles.

Approval Year

PubMed

PubMed

TitleDatePubMed
Name Type Language
MEGALOMICIN POTASSIUM PHOSPHATE
USAN  
USAN  
Official Name English
SCH 13430.2KH
Code English
MEGALOMICIN A COMPOUND WITH POTASSIUM DIHYDROGEN PHOSPHATE (1:2)
Common Name English
SCH 13430.2KH2PO4
Code English
MEGALOMICIN POTASSIUM PHOSPHATE [USAN]
Common Name English
SCH 13430.2KH(SUB 2)PO(SUB 4)
Code English
Code System Code Type Description
PUBCHEM
31863
Created by admin on Fri Dec 15 15:05:09 GMT 2023 , Edited by admin on Fri Dec 15 15:05:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110742
Created by admin on Fri Dec 15 15:05:09 GMT 2023 , Edited by admin on Fri Dec 15 15:05:09 GMT 2023
PRIMARY
CAS
51481-68-6
Created by admin on Fri Dec 15 15:05:09 GMT 2023 , Edited by admin on Fri Dec 15 15:05:09 GMT 2023
SUPERSEDED
FDA UNII
P368DJZ2JM
Created by admin on Fri Dec 15 15:05:09 GMT 2023 , Edited by admin on Fri Dec 15 15:05:09 GMT 2023
PRIMARY
NCI_THESAURUS
C174829
Created by admin on Fri Dec 15 15:05:09 GMT 2023 , Edited by admin on Fri Dec 15 15:05:09 GMT 2023
PRIMARY
CAS
23319-48-4
Created by admin on Fri Dec 15 15:05:09 GMT 2023 , Edited by admin on Fri Dec 15 15:05:09 GMT 2023
PRIMARY