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Details

Stereochemistry ABSOLUTE
Molecular Formula C50H78N2O18
Molecular Weight 995.1569
Optical Activity UNSPECIFIED
Defined Stereocenters 19 / 19
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMPHAMIDE

SMILES

[H][C@]12C[C@@H](O[C@]3([H])O[C@H](C)[C@@H](O)[C@H](NC(=O)CCN)[C@@H]3O)\C=C\C=C\C=C\C=C\C=C\C=C\C=C\[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]1C(O)=O)O2

InChI

InChIKey=CYJBHAVTMPSGMH-UDCSRDJTSA-N
InChI=1S/C50H78N2O18/c1-29-17-15-13-11-9-7-5-6-8-10-12-14-16-18-36(69-49-47(63)44(46(62)32(4)68-49)52-41(59)21-22-51)26-40-43(48(64)65)39(58)28-50(66,70-40)27-35(55)24-38(57)37(56)20-19-33(53)23-34(54)25-42(60)67-31(3)30(2)45(29)61/h5-18,29-40,43-47,49,53-58,61-63,66H,19-28,51H2,1-4H3,(H,52,59)(H,64,65)/b6-5+,9-7+,10-8+,13-11+,14-12+,17-15+,18-16+/t29-,30-,31-,32+,33+,34+,35-,36-,37+,38+,39-,40-,43+,44-,45+,46+,47-,49-,50+/m0/s1

HIDE SMILES / InChI

Molecular Formula C50H78N2O18
Molecular Weight 995.1569
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 19 / 19
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:51:19 GMT 2023
Edited
by admin
on Sat Dec 16 18:51:19 GMT 2023
Record UNII
WH2AF65BVL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMPHAMIDE
Common Name English
(1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-(((2R,3S,4S,5S,6R)-4-(3-AMINOPROPANAMIDO)-3,5-DIHYDROXY-6-METHYLTETRAHYDRO-2H-PYRAN-2-YL)OXY)-1,3,5,6,9,11,17,37-OCTAHYDROXY-15,16,18-TRIMETHYL-13-OXO-14,39-DIOXABICYCLO(
Systematic Name English
AMPHOTERICIN B N-(2-AMINOETHYL)AMIDE
Common Name English
Code System Code Type Description
PUBCHEM
162623740
Created by admin on Sat Dec 16 18:51:19 GMT 2023 , Edited by admin on Sat Dec 16 18:51:19 GMT 2023
PRIMARY
FDA UNII
WH2AF65BVL
Created by admin on Sat Dec 16 18:51:19 GMT 2023 , Edited by admin on Sat Dec 16 18:51:19 GMT 2023
PRIMARY
CAS
2499888-87-6
Created by admin on Sat Dec 16 18:51:19 GMT 2023 , Edited by admin on Sat Dec 16 18:51:19 GMT 2023
PRIMARY
Related Record Type Details
TARGET ORGANISM->INHIBITOR
48 HR MIC COMPARES TO 0.25 FOR Amphotericin B
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