Forodesine
Modify Date: 2024-01-13 07:39:00
Forodesine structure
|
Common Name | Forodesine | ||
|---|---|---|---|---|
| CAS Number | 209799-67-7 | Molecular Weight | 266.25300 | |
| Density | 2.01 | Boiling Point | 613.5ºC at 760mmHg | |
| Molecular Formula | C11H14N4O4 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 324.8ºC | |
Use of ForodesineForodesine(BCX-1777 freebase; Immucillin-H) is an orally bioavailable PNP inhibitor with picomolar potency; induces apoptosis, mainly in T cells.IC50 value:Target: PNP inhibitorForodesine and ara-G cytotoxicities were higher in T-cell acute lymphoblastic leukemia (T-ALL) samples than in B-cell precursor (BCP)-ALL and acute myeloid leukemia (AML) samples. Resistance to forodesine did not preclude ara-G sensitivity and vice versa, indicating that both drugs rely on different resistance mechanisms [1]. BCX1777 was well tolerated at doses up to 300 mg once daily and showed preliminary evidence of activity in relapsed or refractory peripheral T/natural killer-cell malignancies, warranting further investigation [2]. after 48 hours of treatment with forodesine there was a slight dGTP increase in 5T33MM and RPMI-8226 MM cells associated with partial inhibition of proliferation and a limited induction of apoptosis [3]. In the presence of 10 μM deoxyguanosine, forodesine effectively inhibited the growth of CEM cells but not that of CEM/ara-G cells [4]. |
| Name | immucillin H |
|---|---|
| Synonym | More Synonyms |
| Description | Forodesine(BCX-1777 freebase; Immucillin-H) is an orally bioavailable PNP inhibitor with picomolar potency; induces apoptosis, mainly in T cells.IC50 value:Target: PNP inhibitorForodesine and ara-G cytotoxicities were higher in T-cell acute lymphoblastic leukemia (T-ALL) samples than in B-cell precursor (BCP)-ALL and acute myeloid leukemia (AML) samples. Resistance to forodesine did not preclude ara-G sensitivity and vice versa, indicating that both drugs rely on different resistance mechanisms [1]. BCX1777 was well tolerated at doses up to 300 mg once daily and showed preliminary evidence of activity in relapsed or refractory peripheral T/natural killer-cell malignancies, warranting further investigation [2]. after 48 hours of treatment with forodesine there was a slight dGTP increase in 5T33MM and RPMI-8226 MM cells associated with partial inhibition of proliferation and a limited induction of apoptosis [3]. In the presence of 10 μM deoxyguanosine, forodesine effectively inhibited the growth of CEM cells but not that of CEM/ara-G cells [4]. |
|---|---|
| Related Catalog | |
| References |
| Density | 2.01 |
|---|---|
| Boiling Point | 613.5ºC at 760mmHg |
| Molecular Formula | C11H14N4O4 |
| Molecular Weight | 266.25300 |
| Flash Point | 324.8ºC |
| Exact Mass | 266.10200 |
| PSA | 134.26000 |
| Vapour Pressure | 6.61E-16mmHg at 25°C |
| Index of Refraction | 1.894 |
| Isopamphos |
| Fodosine |
| Immucillin-H |
| Forodesine |