구조모아 (StructureMoa)항암 chemical structure spider web
방문타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일
현재 선택: 1개 · 임상 갱신 필요 1개
프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.
표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.
| 항목 | |
|---|---|
Overview Program | Celecoxib |
Overview Company | Pfizer's Upjohn has merged with Mylan to form Viatris Inc. |
Overview Modality | ANTIBODY |
Overview Target | FRα |
Overview Indication | Malignant Neoplasm of Pancreas Metastatic to Peritoneal Surface; Malignant Peritoneal Mesothelioma |
Overview Phase | PHASE_2 |
Overview Status | ACTIVE |
Overview Content status | Limited Data |
Overview Data Confidence | Data Confidence · Low |
Overview Development Signal | Development Signal · Emerging |
Overview Approval status | Investigational |
MoA Mechanism | targeting MAPK and NF-κB pathway |
MoA Biomarker | biomarkers and prioritize druggable therapeutic targets for AD |
PK/PD Half-life | 11 h |
PK/PD Species | Mouse |
PK/PD Animal (cat.) | Mouse, In vitro |
PK/PD Experiment | Pharmacokinetic |
Toxicology Species | Mouse |
Toxicology Animal (cat.) | Mouse, In vitro |
Toxicology Major finding | Design, synthesis, molecular docking and molecular dynamics simulations of pyrazolo[3,4- d ]pyrimidine scaffolds as selective COX-2 and CDK2 kinase inhibitors with dual anti-inflammatory and anti-proliferative activities.. A new series of pyrazolo[3,4- d ]pyrimidine scaffolds, namely, 4a-l, were designed, synthesized, and tested for anti-inflammatory and anti-proliferative activities. Compounds 4f… |
Toxicology CRS | Reported |
Clinical Safety signal | Design, synthesis, molecular docking and molecular dynamics simulations of pyrazolo[3,4- d ]pyrimidine scaffolds as selective COX-2 and CDK2 kinase inhibitors with dual anti-inflammatory and anti-proliferative activities.. A new series of pyrazolo[3,4- d ]pyrimidine scaffolds, namely, 4a-l, were designed, synthesized, and tested for anti-inflammatory and anti-proliferative activities. Compounds 4f… |
Clinical Selected reported efficacy | ORR 21% |
Clinical Reported ORR | 21% |
Clinical Result source | ClinicalTrials.gov NCT02192190 |
Clinical Program phase | PHASE_2 |
Clinical Trial activity | No active/completed counts |
Clinical Trial ref | NCT02192190 |
타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일
현재 선택: 1개 · 임상 갱신 필요 1개
프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.
표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.
| 항목 | |
|---|---|
Overview Program | Celecoxib |
Overview Company | Pfizer's Upjohn has merged with Mylan to form Viatris Inc. |
Overview Modality | ANTIBODY |
Overview Target | FRα |
Overview Indication | Malignant Neoplasm of Pancreas Metastatic to Peritoneal Surface; Malignant Peritoneal Mesothelioma |
Overview Phase | PHASE_2 |
Overview Status | ACTIVE |
Overview Content status | Limited Data |
Overview Data Confidence | Data Confidence · Low |
Overview Development Signal | Development Signal · Emerging |
Overview Approval status | Investigational |
MoA Mechanism | targeting MAPK and NF-κB pathway |
MoA Biomarker | biomarkers and prioritize druggable therapeutic targets for AD |
PK/PD Half-life | 11 h |
PK/PD Species | Mouse |
PK/PD Animal (cat.) | Mouse, In vitro |
PK/PD Experiment | Pharmacokinetic |
Toxicology Species | Mouse |
Toxicology Animal (cat.) | Mouse, In vitro |
Toxicology Major finding | Design, synthesis, molecular docking and molecular dynamics simulations of pyrazolo[3,4- d ]pyrimidine scaffolds as selective COX-2 and CDK2 kinase inhibitors with dual anti-inflammatory and anti-proliferative activities.. A new series of pyrazolo[3,4- d ]pyrimidine scaffolds, namely, 4a-l, were designed, synthesized, and tested for anti-inflammatory and anti-proliferative activities. Compounds 4f… |
Toxicology CRS | Reported |
Clinical Safety signal | Design, synthesis, molecular docking and molecular dynamics simulations of pyrazolo[3,4- d ]pyrimidine scaffolds as selective COX-2 and CDK2 kinase inhibitors with dual anti-inflammatory and anti-proliferative activities.. A new series of pyrazolo[3,4- d ]pyrimidine scaffolds, namely, 4a-l, were designed, synthesized, and tested for anti-inflammatory and anti-proliferative activities. Compounds 4f… |
Clinical Selected reported efficacy | ORR 21% |
Clinical Reported ORR | 21% |
Clinical Result source | ClinicalTrials.gov NCT02192190 |
Clinical Program phase | PHASE_2 |
Clinical Trial activity | No active/completed counts |
Clinical Trial ref | NCT02192190 |
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