AMPHAMIDE

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 Search

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


					4D7G21HDBC

CANDIDA ALBICANS

TARGET ORGANISM->INHIBITOR

Comments:

48 HR MIC COMPARES TO 0.25 FOR Amphotericin B

Qualification:

MIC

Amount: