Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H30N6O2S |
Molecular Weight | 442.578 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C1=C(SC2=NC3=C(C=CN=C3N)N2CCNCC(C)(C)C)C=C4OCOC4=C1
InChI
InChIKey=RVJIQAYFTOPTKK-UHFFFAOYSA-N
InChI=1S/C22H30N6O2S/c1-22(2,3)12-24-8-9-28-14-6-7-25-20(23)19(14)26-21(28)31-18-11-17-16(29-13-30-17)10-15(18)27(4)5/h6-7,10-11,24H,8-9,12-13H2,1-5H3,(H2,23,25)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/19952121Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/19509149
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19952121
Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/19509149
CUDC-305, is a novel heat shock protein 90 (HSP90) inhibitor with strong affinity for HSP90 alpha/beta, high oral bioavailability and potent anti-proliferative activity against a broad range of cancer cell lines (with a mean IC50 of 220 nmol/L), including many non-small cell lung cancer (NSCLC) cell lines which are resistant to standard-of-care (SOC) agents. In both laboratory and animal testing, CUDC-305 demonstrated high potency in vitro and/or in vivo across a wide range of cancers. Most notably, Curis scientists observed complete tumor regression following oral administration of CUDC-305 in a mouse xenograft model of acute myelogenous leukemia (AML). Tumor regression has also been observed after treatment of CUDC-305 in mouse xenograft models of breast, non-small cell lung, gastric cancer and glioblastoma brain cancers. In this preclinical testing, the compound also demonstrated an ability to effectively cross the blood brain barrier, and demonstrated an ability to extend survival in an intracranial glioblastoma model. Early stage toxicity studies suggest that CUDC-305 appears to have a better therapeutic window than several leading Hsp90 inhibitors in clinical development.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19509149
Curator's Comment: CUDC-305 can cross blood-brain barrier and reach therapeutic levels in brain tissue.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01168752
Gelatin capsules of 2 dosage strengths (25 mg or 100 mg) The maximum dose will depend on the number of dose levels necessary to determine the MTD. CUDC-305 will be administered orally to sequential escalating dose cohorts, as an every-other-day schedule.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19952121
CUDC-305 strongly bind to cancer-derived
HSP90 complex with an IC50 of 61.2 nmol/L in
H1975 and 74.2 nmol/L in H1993, respectively. 1 umol/L CUDC-305 reduced the levels of phospho-MET
as well as total MET in H1993 and H1975 NSCLC cells
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CUDC-305
Created by
admin on Sat Dec 16 08:24:39 GMT 2023 , Edited by admin on Sat Dec 16 08:24:39 GMT 2023
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PRIMARY | Catalog No. A12648: CUDC-305 (DEBIO-0932)Quick Overview: Debio 0932 is a novel heat shock protein 90 (HSP90) inhibitor with strong affinity for HSP90 alpha/beta, high oral bioavailability and potent anti-proliferative activity against a broad range of cancer cell lines (with a mean IC50 of 220 nmol/L), including many non-small cell lung cancer (NSCLC) cell lines which are resistant to standard-of-care (SOC) agents. | ||
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44156921
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300000042383
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DEBIO-0932
Created by
admin on Sat Dec 16 08:24:39 GMT 2023 , Edited by admin on Sat Dec 16 08:24:39 GMT 2023
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PRIMARY | Biological Activity of Debio 0932:Debio 0932 (CUDC-305) is a novel heat shock protein 90 (HSP90) inhibitor trong affinity for HSP90 alpha/beta, high oral bioavailability and potent anti-proliferative activity against a broad range of cancer cell lines (with a mean IC50 of 220 nmol/L).target: HSP90IC50: 220 nmol/Lin vitro: H1993 and H1975 NSCLC cells were incubated with 1 .MU.mol/L CUDC-305 for 7 hours and then cultured in compound-free medium for an additional 0, 17, or 24 hours, respectively, before being analyzed by Western blotin vivo: CUDC-305 was delivered through oral gavage on an every-other-day (once every two days) dosing schedule at various doses up to 160 mg/kg-its maximum tolerated dose in nude mice. In survival studies in Balb/C nude mice, the highest dose was reduced to 120 mg/kg as a result of the compromised animal condition due to lung and brain tumor implantation surgeries. | ||
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0V278OKN9G
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C92572
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DTXSID10657665
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1061318-81-7
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ACTIVE MOIETY