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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H29N4O11.Na
Molecular Weight 500.4328
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALMURTIDE SODIUM

SMILES

[Na+].C[C@H](NC(=O)CO[C@@H]([C@H](O)[C@H](O)CO)[C@@H](NC(C)=O)C=O)C(=O)N[C@H](CCC([O-])=O)C(N)=O

InChI

InChIKey=LWDLWMRHPMEHTA-FRSJEOSWSA-M
InChI=1S/C18H30N4O11.Na/c1-8(18(32)22-10(17(19)31)3-4-14(28)29)20-13(27)7-33-16(15(30)12(26)6-24)11(5-23)21-9(2)25;/h5,8,10-12,15-16,24,26,30H,3-4,6-7H2,1-2H3,(H2,19,31)(H,20,27)(H,21,25)(H,22,32)(H,28,29);/q;+1/p-1/t8-,10+,11-,12+,15+,16+;/m0./s1

HIDE SMILES / InChI
Almurtide (CGP 11637) is a synthetic muramyl dipeptide (MDP) analogue with potential immunostimulating and antineoplastic activity. As a derivative of the mycobacterial cell wall component MDP, almurtide activates both monocytes and macrophages. This results in the secretion of cytokines and induces the recruitment and activation of other immune cells, which may result in indirect tumoricidal or cytostatic effects. CGP 11637 has been shown to prevent oncogenic viral infections in mice.

Approval Year

PubMed

PubMed

TitleDatePubMed
Prevention of oncogenic viral infections in mice with CGP 11637, a synthetic muramyl dipeptide analog.
1985-11
Patents

Patents

Sample Use Guides

Mice were injected with 100 ug of Almurtide s.c. at 1-to 2-month intervals
Route of Administration: Other
Name Type Language
ALMURTIDE SODIUM
Common Name English
D-.ALPHA.-GLUTAMINE, N2-(N-(N-ACETYLNORMURAMOYL)-L-ALANYL)-, MONOSODIUM SALT
Preferred Name English
Code System Code Type Description
CAS
103882-13-9
Created by admin on Tue Apr 01 17:29:10 GMT 2025 , Edited by admin on Tue Apr 01 17:29:10 GMT 2025
PRIMARY
FDA UNII
G09BIN46IX
Created by admin on Tue Apr 01 17:29:10 GMT 2025 , Edited by admin on Tue Apr 01 17:29:10 GMT 2025
PRIMARY
PUBCHEM
121596538
Created by admin on Tue Apr 01 17:29:10 GMT 2025 , Edited by admin on Tue Apr 01 17:29:10 GMT 2025
PRIMARY