Compound - Results

Amphotericin B

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Information Structure
Name Amphotericin B
Synonyms
(1R-(1R*,3S*,5R*,6R*,9R*,11R*,15S*,16R*,17R*,18S*,19E,21E,23E,25E,27E,29E,31E,33R*,35S*,36R*,37S*))-33-((3-Amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy
14,39-Dioxabicyclo(33.3.1)nonatriaconta-19,21,23,25,2 7,29,31-heptaene-36-carboxylic Acid, 33-((3-amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy)-1,3,5,6
5-18-10-00525 (Beilstein Handbook Reference)
Abelcet
ABLC
AI3-26528
Ambisome
Amfotericina B
Ampho-Moronal
Amphocin
Amphomoronal
Amphotericin B
AmphotericinB
Amphotericine B
Amphotericinum B
Amphozone
BRN 0078342
BU2690300
CCRIS 5963
component Of Talsutin
DRG-0096
EINECS 215-742-2
Fungilin
Fungizone
HSDB 3008
IAB
Liposomal Amphotericin B
Mysteclin-F
NS 718
NSC 527017
Tegopen
ATC A01AB04
A07AA07
D01AA10
G01AA03
J02AA01
CID 14956
CAS 001397893
TTD Drug ID DAP001322
SMILES C[C@H]1O[C@@H](O[C@@H]2C[C@@H]3O[C@](O)(C[C@@H](O)C[C@@H](O)[C@H](O)CC[C@@H](O)C[C@@H](O)CC(=O)O[C@@H](C)[C@H](C)[C@H](O)[C@@H](C)C=CC=CC=CC=CC=CC=CC=C2)C[C@H](O)[C@H]3C(O)=O)[C@@H](O)[C@@H](N)[C@@H]1O
Formula C47H73NO17
Molweight 924.079
Atoms 83
LogP 1.412
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 18
Extrarenal fraction 0.95
Elimination half-life 15 days
Hachimycin

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Information Structure
Name hachimycin
Synonyms
12698-99-6
12699-00-2
33-(3-amino-3,6-dideoxy-b-d-mannopyranosyloxy)-17-[6-(4-aminophenyl)- 4-hydroxy-1-methyl-6-oxohexyl]-1,3,5,9,11,37-hexahydroxy-18-methyl-13,15- Dioxo-
5,27,29,31-heptaene-36-carboxylic Acid & 33-(3-amino-3,6-dideoxy-b-d-mannopyranosyloxy)-17-[6-(4-aminophenyl)-4-hydroxy-1-methyl-6-oxohexyl]-1,3,5,7,9
hachimycin
icyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic Acid
trichomycin
ATC D01AA03
G01AA06
J02AA02
CID 11979956
CAS cid11979956
Formula C47H73NO17
Molweight 924.079
Atoms 83
LogP 1.412
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 18