U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H22Cl2N2O4
Molecular Weight 305.199
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MANNOMUSTINE

SMILES

O[C@H](CNCCCl)[C@@H](O)[C@H](O)[C@H](O)CNCCCl

InChI

InChIKey=MQXVYODZCMMZEM-ZYUZMQFOSA-N
InChI=1S/C10H22Cl2N2O4/c11-1-3-13-5-7(15)9(17)10(18)8(16)6-14-4-2-12/h7-10,13-18H,1-6H2/t7-,8-,9-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H22Cl2N2O4
Molecular Weight 305.199
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Mannomustine is a substance synthesized as one of a series of compounds linking the actively cytotoxic chemical group beta-chlorethylamine with a naturally occurring substance, mannitol. Mannomustine is an alkylating agent with antineoplastic properties. It was being studied in the treatment of hematologic malignancies.

Originator

Curator's Comment: reference retrieved from https://www.ncbi.nlm.nih.gov/pubmed/13671231

Approval Year

PubMed

PubMed

TitleDatePubMed
Mannomustine in treatment of leukaemias, polycythaemia, and malignant disorders.
1959 Aug 22
Clinical results after 5 years of treatment of tumours and leukaemias with degranol (Mannomustine).
1961 Oct
Mannomustine (dihydrochloride).
1975

Sample Use Guides

the maximal single dose is 100 mg daily or on alternate days
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:56:04 GMT 2023
Edited
by admin
on Sat Dec 16 17:56:04 GMT 2023
Record UNII
E60VWA40D2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MANNOMUSTINE
INN  
INN  
Official Name English
1,6-BIS((2-CHLOROETHYL)AMINO)-1,6-DIDEOXY-D-MANNITOL
Systematic Name English
NSC-9698 FREE BASE
Code English
BCM
Code English
mannomustine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C697
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
Code System Code Type Description
INN
759
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
DRUG CENTRAL
1633
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
FDA UNII
E60VWA40D2
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
ChEMBL
CHEMBL1908338
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
WIKIPEDIA
Mannomustine
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
CAS
576-68-1
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
NCI_THESAURUS
C2070
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
EVMPD
SUB08643MIG
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
PUBCHEM
3033867
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID9020798
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-404-3
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
SMS_ID
100000081741
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
MESH
D008357
Created by admin on Sat Dec 16 17:56:04 GMT 2023 , Edited by admin on Sat Dec 16 17:56:04 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY