Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C41H47Cl2NO6 |
Molecular Weight | 720.721 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](OC(=O)COC(=O)CCCC3=CC=C(C=C3)N(CCCl)CCCl)[C@@]1(C)CC[C@]4([H])C5=C(CC[C@@]24[H])C=C(OC(=O)C6=CC=CC=C6)C=C5
InChI
InChIKey=IFJUINDAXYAPTO-UUBSBJJBSA-N
InChI=1S/C41H47Cl2NO6/c1-41-21-20-34-33-17-15-32(49-40(47)29-7-3-2-4-8-29)26-30(33)12-16-35(34)36(41)18-19-37(41)50-39(46)27-48-38(45)9-5-6-28-10-13-31(14-11-28)44(24-22-42)25-23-43/h2-4,7-8,10-11,13-15,17,26,34-37H,5-6,9,12,16,18-25,27H2,1H3/t34-,35-,36+,37+,41+/m1/s1
Atrimustine [bestrabucil, busramustine, KM 2210, kregan], a conjugate of estradiol and chlorambucil, is a DNA antagonist that was developed by Kureha Corporation (Japan). Atrimustine is an antineoplastic drug that was used for the treatment of breast cancer, non-Hodgkin's lymphoma, as well as Graft-versus-host disease. Side effects of atrimustine in clinical trials included vaginal bleeding and gynecomastia. Atrimustine reached preregistration in Japan for the treatment of cancer, however, its development has been discontinued.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2877106
Curator's Comment: Atrimustine is considered to be useful for the treatment of advanced and recurrent breast cancer when administered at a dose level of 200 mg per day for more than 4 weeks. https://www.ncbi.nlm.nih.gov/pubmed/8135468
Thirteen patients with hematological neoplasms were treated with Atrimustine (100 mg/day po, total dose 700-9,900 mg).
Route of Administration:
Oral
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C574
Created by
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NCI_THESAURUS |
C697
Created by
admin on Sat Dec 16 18:05:27 GMT 2023 , Edited by admin on Sat Dec 16 18:05:27 GMT 2023
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Atrimustine
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100000086637
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DTXSID501046416
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SUB05605MIG
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C1348
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CHEMBL2106381
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XC0K09B7K4
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6407
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6917688
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75219-46-4
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ACTIVE MOIETY