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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8452 | Dantrolene | Others | |
Dantrolene is a postsynaptic muscle relaxant by inhibiting Ca2+ ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors. | |||
T22223 | 3PO | Glucokinase , Autophagy | |
3PO is a small-molecule inhibitor of PFKFB3 (IC50: 22.9 μM), inhibiting the proliferation of several human malignant hematopoietic and adenocarcinoma cell lines (IC50: 1.4-24 μM). It suppresses glucose uptake, and decrea... | |||
T2379 | UNC1215 | Apoptosis , Epigenetic Reader Domain , Histone Methyltransferase | |
UNC1215, an effective and specific MBT (malignant brain tumor) antagonist, binds L3MBTL3 (IC50/Kd: 40/120 nM). The selectivity of UNC1215 for L3MBTL3 is 50-fold higher versus other members of the human MBT family. | |||
T14214 | AMG 511 | PI3K | |
AMG 511 is a potent and orally available pan inhibitor of class I PI3Ks(Kis of 4 nM, 6 nM, 2 nM and 1 nM for PI3Kα, β, δ and γ, respectively). It exhibits anti-tumor activity in mouse glioblastoma xenograft model[1]. AMG... | |||
T1973 | PFI-4 | PFI4 | Epigenetic Reader Domain |
PFI-4 is a potent and selective and cell-permeable BRPF1 bromodomain inhibitor. | |||
TN2069 | Picrocrocin | Apoptosis | |
Picrocrocin is a natural product | |||
T9954 | K-975 | Others | |
K-975 is a highly selective, orally active TEAD inhibitor, effectively inhibiting protein-protein interactions between TEAD and YAP1/TAZ. | |||
T1120 | Dacarbazine | Imidazole Carboxamide,DTIC-Dome | Apoptosis , Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis |
Dacarbazine (DTIC-Dome) is an antineoplastic agent. It has significant activity against melanomas. | |||
T38050 | CP-609754 | Transferase | |
CP-609754 (LNK-754) is a potent and reversible farnesyltransferase inhibitor with potential anticancer activity.The IC50 for inhibiting farnesylation of recombinant human H-Ras is 0.57 ng/mL and recombinant K-Ras is 46 n... | |||
T21505 | Suberoyl bis-hydroxamic acid | SBHA,Suberohydroxamic acid | Apoptosis , HDAC |
Suberoyl bis-hydroxamic acid (SBHA) is a Histone deacetylase (HDAC) inhibitor. HDAC is required for transcriptional modulation, cell cycle regulation and development. It is an enzyme that deacetylates lysine residues on ... | |||
T16699 | PYZD-4409 | Others , E1/E2/E3 Enzyme | |
PYZD-4409 is a selective UBA1 inhibitor with an IC50 of 20 μM. PYZD-4409 induces cell death in malignant cells and is preferentially cytotoxic to malignant cells over normal hematopoietic cells. | |||
TNU0123 | 5-Methoxyuridine | Mo5U | Apoptosis |
5-Methoxyuridine (Mo5U) is a purine nucleoside analog with a broad spectrum of antitumor activity, targeting malignant tumors of the inert lymphatic system and inducing apoptosis.5-Methoxyuridine's anticancer mechanism i... | |||
T76815 | Lexatumumab | ETR2-ST01,DR5 mAB,HGS-ETR 2 | Apoptosis |
Lexatumumab (GHS-ETR 2) is a human excitatory monoclonal antibody targeting TRAIL receptor 2 that has anticancer activity and induces apoptosis in malignant mesothelioma. Lexatumumab can be used to study malignant pleura... | |||
T67839 | HG106 | Others | |
HG106, which is anti-inflammatory and may be used to treat the growth of diseases such as malignant tumours caused by mutations in the RAS gene., which is anti-inflammatory and may be used to treat the growth of diseases... | |||
TNU0436 | 2-Thiocytidine | Apoptosis , Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis | |
2-Thiocytidine is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and has a broad spectrum of antitumor activity.2-Thiocytidine induces apoptosis by inhibiting DNA synthesis.2-Thioc... | |||
T8762 | SW106065 | SW-106065 | Apoptosis |
SW106065 is a novel pharmacologic inducer of apoptosis in MPNST (malignant peripheral nerve sheath tumors).SW106065 is an apoptosis inducer in malignant peripheral nerve sheath tumors (MPNST). It inhibits ATP consumption... | |||
T8654 | Plx-4032 | Vemurafenib | Raf |
Plx-4032 (Vemurafenib) is a small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma. | |||
T7491 | 6-O-Methyl Guanosine | Nucleoside Antimetabolite/Analog | |
6-O-Methyl Guanosine inhibit colony-forming ability in a malignant xeroderma pigmentosum cell line. | |||
T77689 | (1R,2R)-(-)-1,2-Diaminocyclohexane | (1R,2R)-Cyclohexane-1,2-diamin | Others |
(1R,2R)-(-)-1,2-Diaminocyclohexane ((1R,2R)-Cyclohexane-1,2-diamin) has anticancer and antitumor activity and can be used to study malignant tumors. | |||
T2068 | (Rac)-LB-100 | Phosphatase | |
LB-100, a novel Protein Phosphatase 2A (PP2A) inhibitor, sensitizes malignant meningioma cells to the therapeutic effects of radiation |