chlorobromofosfamide: the bromo analog of ifosfamide [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
ID Source | ID |
---|---|
PubMed CID | 126997 |
CHEMBL ID | 336035 |
SCHEMBL ID | 9062899 |
MeSH ID | M0257455 |
Synonym |
---|
2h-1,3,2-oxazaphosphorin-2-amine, tetrahydro-3-(2-bromoethyl)-n-(2-chloroethyl)-, 2-oxide, (+-)- |
2h-1,3,2-oxazaphosphorin-2-amine, 3-(2-bromoethyl)-n-(2-chloroethyl)tetrahydro-, 2-oxide, (+-)- |
chlorobromofosfamide |
CHEMBL336035 |
cbm 4a |
cbm-4a |
146367-82-0 |
SCHEMBL9062899 |
3-(2-bromoethyl)-2-[(2-chloroethyl)amino]-1,3,2lambda~5~-oxazaphosphinan-2-one |
DTXSID50932822 |
3-(2-bromoethyl)-n-(2-chloroethyl)-2-oxo-1,3,2lambda5-oxazaphosphinan-2-amine |
Excerpt | Reference | Relevance |
---|---|---|
" Ifosfamide, although itself the effective antineoplastic drug useful in situations which have proved refractory to cyclophosphamide therapy, has the side-effect toxicities caused by its metabolities that pose clinically a very real problem." | ( Influence of mesna on urotoxic effects of selected bromosubstituted analogs of ifosfamide. Konarski, L; Kowalski, P; Kuśnierczyk, H; Radzikowski, C, 1997) | 0.3 |
Excerpt | Reference | Relevance |
---|---|---|
"Three bromine-ifosfamide analogues: racemic chlorobromofosfamide (+/-)-(R,S)-1, its levorotatory enantiomer (-)-(S)-2 and racemic bromofosfamide (+/-)-(R,S)-3 showed considerable stereoselective differences in their pharmacokinetics and bioavailability depending on the route of administration and regimen of dosage studies in rats." | ( Pharmacokinetic-stereoselective differentiation of some isomeric analogues of ifosfamide. Hładoń, B; Kinas, R; Kuśnierczyk, H; Laskowska, H; Sloderbach, A; Sochacki, M, ) | 0.13 |
Excerpt | Relevance | Reference |
---|---|---|
"Three bromine-ifosfamide analogues: racemic chlorobromofosfamide (+/-)-(R,S)-1, its levorotatory enantiomer (-)-(S)-2 and racemic bromofosfamide (+/-)-(R,S)-3 showed considerable stereoselective differences in their pharmacokinetics and bioavailability depending on the route of administration and regimen of dosage studies in rats." | ( Pharmacokinetic-stereoselective differentiation of some isomeric analogues of ifosfamide. Hładoń, B; Kinas, R; Kuśnierczyk, H; Laskowska, H; Sloderbach, A; Sochacki, M, ) | 0.13 |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID115147 | Maximum tolerated dose against L1210 leukemia in mice | 2002 | Bioorganic & medicinal chemistry letters, Feb-11, Volume: 12, Issue:3 | Studies on the side-chain hydroxylation of ifosfamide and its bromo analogue. |
AID112166 | Effective dose that produce antitumor activity against L1210 leukemia in mice | 2002 | Bioorganic & medicinal chemistry letters, Feb-11, Volume: 12, Issue:3 | Studies on the side-chain hydroxylation of ifosfamide and its bromo analogue. |
AID211869 | Dose required to induce cytotoxicity against L1210 leukemia in mice | 2002 | Bioorganic & medicinal chemistry letters, Feb-11, Volume: 12, Issue:3 | Studies on the side-chain hydroxylation of ifosfamide and its bromo analogue. |
AID235229 | Therapeutic index represented as LD50/ED50 was determined | 2002 | Bioorganic & medicinal chemistry letters, Feb-11, Volume: 12, Issue:3 | Studies on the side-chain hydroxylation of ifosfamide and its bromo analogue. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (33.33) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.34) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 8 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |