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Details

Stereochemistry ACHIRAL
Molecular Formula C11H15N2O4PS.BrH
Molecular Weight 383.199
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MB-05032 MONOHYDROBROMIDE

SMILES

Br.CC(C)CC1=C(N=C(N)S1)C2=CC=C(O2)P(O)(O)=O

InChI

InChIKey=MKDPXWINJXJYOJ-UHFFFAOYSA-N
InChI=1S/C11H15N2O4PS.BrH/c1-6(2)5-8-10(13-11(12)19-8)7-3-4-9(17-7)18(14,15)16;/h3-4,6H,5H2,1-2H3,(H2,12,13)(H2,14,15,16);1H

HIDE SMILES / InChI

Molecular Formula C11H15N2O4PS
Molecular Weight 302.287
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Managlinat dialanetil (MB06322 or CS-917) is an inhibitor of fructose 1,6-bisphphosphatase. Managlinat dialanetil is a bisamidate prodrug and its activation requires a two-step enzyme catalyzed reaction. Metabasis Therapeutics Inc in collaboration with Daiichi Sankyo Co Ltd was developing managlinat dialanetil for the potential treatment of type 2 diabetes.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
16.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Fructose-1,6-bisphosphatase regulates glucose-stimulated insulin secretion of mouse pancreatic beta-cells.
2010-10
Metformin primarily decreases plasma glucose not by gluconeogenesis suppression but by activating glucose utilization in a non-obese type 2 diabetes Goto-Kakizaki rats.
2009-11-25
CS-917, a fructose 1,6-bisphosphatase inhibitor, improves postprandial hyperglycemia after meal loading in non-obese type 2 diabetic Goto-Kakizaki rats.
2008-12-28
Managlinat dialanetil, a fructose-1,6-bisphosphatase inhibitor for the treatment of type 2 diabetes.
2007-10
Inhibition of fructose 1,6-bisphosphatase reduces excessive endogenous glucose production and attenuates hyperglycemia in Zucker diabetic fatty rats.
2006-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:27:12 GMT 2025
Edited
by admin
on Mon Mar 31 23:27:12 GMT 2025
Record UNII
2RGC6XUB92
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MB-05032 MONOHYDROBROMIDE
Common Name English
(5-(2-AMINO-5-ISOBUTYL-THIAZOL-4-YL)-2-FURYL)PHOSPHONIC ACID HYDROBROMIDE
Preferred Name English
MB05032 MONOHYDROBROMIDE
Common Name English
PHOSPHONIC ACID, (5-(2-AMINO-5-(2-METHYLPROPYL)-4-THIAZOLYL)-2-FURANYL)-, MONOHYDROBROMIDE
Systematic Name English
Code System Code Type Description
CAS
261365-09-7
Created by admin on Mon Mar 31 23:27:12 GMT 2025 , Edited by admin on Mon Mar 31 23:27:12 GMT 2025
PRIMARY
PUBCHEM
156613512
Created by admin on Mon Mar 31 23:27:12 GMT 2025 , Edited by admin on Mon Mar 31 23:27:12 GMT 2025
PRIMARY
FDA UNII
2RGC6XUB92
Created by admin on Mon Mar 31 23:27:12 GMT 2025 , Edited by admin on Mon Mar 31 23:27:12 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY