Prednimustine |
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| Trade names | Mostarina, Sterecyst |
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| Other names | EORTC 1502; Leo 1031; NSC 134087; Prednisolone 21-(4-(4-(bis(2-chloroethyl)-amino)phenyl)butanoate); 11β,17α-Dihydroxy-3,20-dioxopregna-1,4-dien-21-yl 4-{4-[bis(2-chloroethyl)amino]-phenyl}butanoate |
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| ATC code | |
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[2-[(8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] 4-[4-[bis(2-chloroethyl)amino]phenyl]butanoate
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| CompTox Dashboard (EPA) | |
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| ECHA InfoCard | 100.044.904 |
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| Formula | C35H45Cl2NO6 |
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| Molar mass | 646.65 g·mol−1 |
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| 3D model (JSmol) | |
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C[C@]12C[C@@H]([C@H]3[C@H]([C@@H]1CC[C@@]2(C(=O)COC(=O)CCCc4ccc(cc4)N(CCCl)CCCl)O)CCC5=CC(=O)C=C[C@]35C)O
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InChI=1S/C35H45Cl2NO6/c1-33-14-12-26(39)20-24(33)8-11-27-28-13-15-35(43,34(28,2)21-29(40)32(27)33)30(41)22-44-31(42)5-3-4-23-6-9-25(10-7-23)38(18-16-36)19-17-37/h6-7,9-10,12,14,20,27-29,32,40,43H,3-5,8,11,13,15-19,21-22H2,1-2H3/t27-,28-,29-,32+,33-,34-,35-/m0/s1 NKey:HFVNWDWLWUCIHC-GUPDPFMOSA-N N
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N Y (what is this?) (verify) |
Prednimustine, sold under the brand names Mostarina and Sterecyst, is a medication which is used in chemotherapy in the treatment of leukemias and lymphomas.[1][2][3] It is the ester formed from two other drugs, prednisolone and chlorambucil.[1][2][3] Rarely, it has been associated with myoclonus.[4]
See also
- List of hormonal cytostatic antineoplastic agents
- List of corticosteroid esters
References
Intracellular chemotherapeutic agents / antineoplastic agents (L01) |
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SPs/MIs (M phase) | | Block microtubule assembly | |
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| Block microtubule disassembly |
- Taxanes (Cabazitaxel
- Docetaxel#
- Larotaxel
- Ortataxel†
- Paclitaxel#
- Tesetaxel)
- Epothilones (Ixabepilone)
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DNA replication inhibitor | DNA precursors/ antimetabolites (S phase) | | Folic acid | |
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| Purine | |
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| Pyrimidine |
- DNA polymerase inhibitor (Cytarabine# +daunorubicin)
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| Deoxyribonucleotide | |
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Topoisomerase inhibitors (S phase) | | I |
- Camptotheca (Belotecan
- Camptothecin
- Cositecan†
- Etirinotecan pegol†
- Exatecan
- Gimatecan
- Irinotecan#
- Lurtotecan‡
- Rubitecan‡
- Silatecan§
- Topotecan)
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| II | |
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| II+Intercalation | |
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Crosslinking of DNA (CCNS) | | Alkylating | |
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| Platinum-based | |
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| Nonclassical | |
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| Intercalation | |
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| Photosensitizers/PDT | |
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| Other | | Enzyme inhibitors |
- FI (Tipifarnib§)
- CDK inhibitors (Abemaciclib
- Alvocidib†
- Palbociclib
- Ribociclib
- Seliciclib†)
- PrI
- PhI (Anagrelide)
- IMPDI (Tiazofurin§)
- LI (Masoprocol)
- PARP inhibitor (Fuzuloparib
- Niraparib +abiraterone acetate
- Olaparib
- Rucaparib)
- HDAC (Belinostat
- Entinostat
- Panobinostat
- Romidepsin
- Vorinostat)
- PIKI (Pi3K) (Alpelisib
- Copanlisib‡
- Duvelisib
- Idelalisib
- Inavolisib
- Umbralisib‡)
- IDH (Enasidenib
- Ivosidenib
- Olutasidenib
- Vorasidenib)
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| Receptor antagonists | |
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| Other/ungrouped |
- Adagrasib
- Aflibercept
- Arsenic trioxide# (Realgar/Indigo naturalis#)
- Asparagine depleters (Asparaginase#/Pegaspargase)
- Axicabtagene ciloleucel
- Belzutifan
- Bexarotene
- Brexucabtagene autoleucel
- Calaspargase pegol
- Celecoxib
- Ciltacabtagene autoleucel
- Darinaparsin
- Demecolcine
- Denileukin diftitox
- Eflornithine
- Elesclomol§
- Elsamitrucin
- Epacadostat
- Eribulin
- Estramustine
- Glasdegib
- Idecabtagene vicleucel
- Idroxioleic acid
- Imetelstat
- Lifileucel
- Lisocabtagene maraleucel
- Lonidamine
- Lucanthone
- Lurbinectedin
- Mitoguazone
- Mitotane
- Nadofaragene firadenovec
- Navitoclax
- Nirogacestat
- Obecabtagene autoleucel
- Oblimersen†
- Omacetaxine mepesuccinate
- Para-toluenesulfonamide
- Pelabresib
- Plitidepsin
- Retinoids (Alitretinoin
- Tretinoin#)
- Selinexor
- Sitimagene ceradenovec
- Sotorasib
- Tabelecleucel
- Tagraxofusp
- Talimogene laherparepvec
- Tazemetostat
- Tebentafusp
- Tiazofurine
- Tigilanol tiglate
- Tisagenlecleucel
- Trabectedin
- Veliparib
- Venetoclax
- Verdinexor
- Vosaroxin
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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Glucocorticoids and antiglucocorticoids (D07, H02) |
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| Glucocorticoids | |
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| Antiglucocorticoids | |
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| Synthesis modifiers | |
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
- See also
- Glucocorticoid receptor modulators
- Mineralocorticoids and antimineralocorticoids
- List of corticosteroids
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Glucocorticoid receptor modulators |
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| GRTooltip Glucocorticoid receptor | | Agonists |
- Others/atypical (other expanded steroid ring systems, homosteroids, and non-pregnane steroids): Cortisuzol
- Cortivazol
- Domoprednate
- Naflocort
- Nicocortonide
- Nivacortol (nivazol)
- Oxisopred
- RU-26988
- RU-28362
- Nonsteroidal glucocorticoids: AZD-5423
- GSK-9027
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Mixed (SEGRMsTooltip Selective glucocorticoid receptor agonists) |
- Dagrocorat
- Fosdagrocorat
- Mapracorat
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| Antagonists |
- 7α-Hydroxy-DHEA
- 17α-Methylprogesterone
- Aglepristone
- Asoprisnil
- Asoprisnil ecamate
- C108297
- C113176
- CORT-108297
- Cyproterone acetate
- Dazucorilant
- Exicorilant (CORT-125281)
- Guggulsterone
- Ketoconazole
- Lilopristone
- LLY-2707
- Metapristone (RU-42633)
- Miconazole
- Mifepristone (RU-486)
- Miricorilant (CORT-118335)
- Onapristone
- ORG-34116
- ORG-34517 (SCH-900636)
- ORG-34850
- Pregnenolone 16α-carbonitrile
- Relacorilant (CORT-125134)
- RTI 3021–012
- RTI 3021–022
- Telapristone
- Tibolone
- Toripristone
- Ulipristal acetate
- Zavacorilant
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| Others |
- Antisense oligonucleotides: IONIS-GCCRRx (ISIS-426115)
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- See also
- Receptor/signaling modulators
- Glucocorticoids and antiglucocorticoids
- Mineralocorticoid receptor modulators
- List of corticosteroids
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