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 (dihydrochloride).
1975
Clinical results after 5 years of treatment of tumours and leukaemias with degranol (Mannomustine).
1961-10
Mannomustine in treatment of leukaemias, polycythaemia, and malignant disorders.
1959-08-22

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 Wed Apr 02 09:48:16 GMT 2025
Edited
by admin
on Wed Apr 02 09:48:16 GMT 2025
Record UNII
E60VWA40D2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MANNOMUSTINE
INN  
INN  
Official Name English
BCM
Preferred Name English
1,6-BIS((2-CHLOROETHYL)AMINO)-1,6-DIDEOXY-D-MANNITOL
Systematic Name English
NSC-9698 FREE BASE
Code English
mannomustine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C697
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
Code System Code Type Description
INN
759
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
DRUG CENTRAL
1633
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
FDA UNII
E60VWA40D2
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
ChEMBL
CHEMBL1908338
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
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WIKIPEDIA
Mannomustine
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
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CAS
576-68-1
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
NCI_THESAURUS
C2070
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
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EVMPD
SUB08643MIG
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
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PUBCHEM
3033867
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
EPA CompTox
DTXSID9020798
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-404-3
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
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SMS_ID
100000081741
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
MESH
D008357
Created by admin on Wed Apr 02 09:48:16 GMT 2025 , Edited by admin on Wed Apr 02 09:48:16 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY