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カタログ番号 | 製品名 | 別名 | ターゲット |
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T18883 | 2-Di-1-ASP | Others | |
2-Di-1-ASP is a mono-stryryl dye and widely used as mitochondrial stain and groove-binding fluorescent probes for double-stranded DNA. It has selective for G-quadruplex (G4) and double-stranded DNA. | |||
T4470 | Pyridostatin TFA | DNA/RNA Synthesis | |
Pyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer with Kd of 490 nM in a cell-free assay, which targets a series of proto-oncogenes including c-kit, K-ras and Bcl-2. | |||
T60028 | MM41 | DNA/RNA Synthesis | |
MM41 is a human telomeric and gene promoter DNA quadruplex stabilizer with an IC50 of <10 nM against the MIA PaCa-2 pancreatic cancer cell line. | |||
T7409 | 360A | DNA/RNA Synthesis , Telomerase | |
360A is a stabilizing G-Quadruplex ligand, and also inhibits telomerase activity for telomerase in TRAP-G4 assay(IC50 : 300 nM). | |||
T13174 | TMPyP4 tosylate | TMP 1363 | DNA/RNA Synthesis , Telomerase |
TMPyP4 tosylate (TMP 1363) is a quadruplex-specific ligand and is a telomerase inhibitor with antitumor effects in osteosarcoma cell lines. | |||
T74613 | G-quadruplex DNA fluorescence probe 1 | ||
Compound E1, also known as G-quadruplex DNA fluorescence probe 1, is a selective fluorescent probe targeting G-quadruplex DNA. It possesses the ability to penetrate membranes and enter living cells, demonstrating low cyt... | |||
T1899 | Pyridostatin | RR82,Pyridostatin Trifluoroacetate Salt | DNA/RNA Synthesis |
Pyridostatin (RR82) is a synthetic small-molecule stabilizer of G-quadruplexes, a secondary structure of DNA that usually exists in the end of the chromosome or the telomeres. | |||
T13584 | BMVC-8C3O | DNA/RNA Synthesis | |
BMVC-8C3O, a DNA G-quadruplex (G4) ligand, induces the topological conversion from non-parallel to parallel forms in human telomeric DNA G4s. | |||
T10352 | APTO-253 | LOR-253,LT-253 | Apoptosis , c-Myc , KLF |
APTO-253 (LOR-253) inhibits c-Myc expression, stabilizes G-quadruplex DNA, and induces cell cycle arrest and apoptosis in acute myeloid leukemia cells. APTO-253 mediates anticancer activity through the induction of the K... | |||
T16703 | Quarfloxin | CX-3543 | DNA/RNA Synthesis |
Quarfloxin (CX-3543) is a fluoroquinolone derivative with antineoplastic activity with IC50 values in the nanomolar range in neuroblastoma cells. Quarfloxin disrupts the interaction between the nucleolin protein and a G-... | |||
T10574 | BMVC | Telomerase | |
BMVC is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor (IC50: ~0.2 μM) with anticancer activities. BMVC inhibits Taq DNA polymerase (IC50: ~2.5 μM). | |||
T30745 | Carboxy-pyridostatin | ||
Carboxy-pyridostatin, as a fluorescent probe, can target G-quadruplex structures and trap cytoplasmic RNA G-quadruplex structures in cells. | |||
T19212 | BMVC2 | o-BMVC | Others |
BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer. | |||
T26892 | Braco-19 | ||
Braco-19 is a G-quadruplex ligand, it inhibits the growth of tumor. | |||
T32014 | GTC365 | GTC 365,NSC 177365,GTC-365,NSC-177365,NSC177365 | |
GTC365 is an hTERT transcriptional repressor that acts in the early stages of the G-quadruplex folding pathway. | |||
T28942 | Telomestatin | SOT 095,GM95,(R)-Telomestatin,GM 95,GM-95 | |
Telomestatin is an inhibitor of the telomerase, it induces the formation of basket-type G-quadruplex (G4) structures from hybrid-type G-quadruplexes in the telomeric region. | |||
T13504 | 360A iodide | 360 A iodide | Telomerase |
360A iodide is a selective stabilizer of G-quadruplex and inhibits telomerase activity (IC50: 300 nM in TRAP-G4 assay). | |||
T13817 | Phen-DC3 | Others | |
Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively). | |||
T33894 | PBP2 | PBP-2,PBP 2 | |
PBP2 is a selective inducer of G-quadruplex structures from the unstructured single-stranded DNA conformations. PBP2 downregulates BCL-2 gene expression in cancer cells. | |||
T26872 | BMVC4 | BMVC 4,BMVC-4 | |
BMVC4 is a G-quadruplex stabilizer. BMVC4 induces senescence by activation of pathways of response to DNA damage that was independent of its telomerase inhibitory activity. | |||
T25255 | CL67 | CL-67,CL 67 | |
CL67 is a hypoxia-inducible factor pathway inhibitor. It acts by binding to a G-quadruplex higher-order structure in the HIF promoter sequence in vitro. | |||
T13817L | Phen-DC3 Trifluoromethanesulfonate | Phen-DC3 Triflate | Others |
T74961 | Anticancer agent 84 | ||
Anticancer Agent 84, a cancer research compound, inhibits c-MYC transcription by stabilizing the G-quadruplex (G4) structure, offering potential for cancer investigation [1]. | |||
T72571 | Antitumor agent-84 | ||
Antitumor Agent-84, a G-quadruplex (G4)-ligand, stabilizes various G4-DNA structures, demonstrating highly effective antitumor properties. | |||
T72572 | Antitumor agent-85 | ||
Antitumor agent-85, a G-quadruplex (G4)-ligand, stabilizes various G4-DNA structures and possesses potent anti-tumor properties. | |||
T37218 | N-methyl Mesoporphyrin IX | ||
N-methyl Mesoporphyrin IX is a widely used G-quadruplex DNA-specific fluorescent binder that effectively monitors Aβ fibrillation. N-methyl Mesoporphyrin IX is sensitive to G-quadruplex DNA and unreactive to duplex, trip... | |||
T73264 | L2H2-6OTD | ||
L2H2-6OTD, a telomeric inhibitor analogue characterized by containing one to four G-quadruplex binding loops, exhibits telomerase inhibitory activity with an IC 50 value of 15 nM. | |||
T63765 | L5-DA | ||
L5-DA is a G-quadruplex (G4) ligand that selectively stabilizes G4s. L5-DA exhibits significant cytotoxicity to HeLa cells with an IC50 value of 4.3 μM. L5-DA stabilizes G4s in HeLa cells and can block the cell cycle and... | |||
T74460 | C-Myc inhibitor 5 | ||
c-Myc Inhibitor 5 (DA3) is a fluorescent bispurine compound with a long-chain bridge that selectively binds to the c-MYC G-quadruplex, exhibiting a dissociation constant (K D) of 16 μM. Unlike other G4-driven oncogenes, ... | |||
T74539 | DIZ-3 | ||
DIZ-3, a selective multimeric G-quadruplex (G4) ligand, employs a G4-ligand-dimerizing approach to intercalate into the G4-G4 interface, thereby stabilizing its higher-order structure. This compound effectively induces c... | |||
T72201 | Pyridostatin hydrochloride | RR82 hydrochloride | |
Pyridostatin (RR82) hydrochloride, a G-quadruplex DNA stabilizing agent (Kd = 490 nM), induces replication- and transcription-dependent DNA damage, promoting growth arrest in human cancer cells. It specifically targets t... |
カタログ番号 | 製品名 | 別名 | ターゲット |
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T5S2361 | Epiberberine | ERK , Beta-Secretase , MEK , BACE , AMPK , AChR , AChE | |
1. Epiberberine may be caused drug interactions based on CYP2D6 enzyme. 2. Epiberberine has anti-adipogenic effect is mediated by downregulation of the Raf/MEK1/ERK1/2 and AMPKα/Akt pathways during 3T3-L1 adipocyte diffe... |
カタログ番号 | 製品名 | Species | Expression System |
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TMPH-01801 | NME2 Protein, Human, Recombinant (His & Myc) | Human | E. coli |
Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate. Negativ... | |||
TMPK-01411 | Peptide Ready HLA-G&B2M Monomer Protein, Human, MHC (His & Avi), Biotinylated | Human | HEK293 |
Peptide Ready HLA-G&B2M Monomer is absent from peptide, namely peptide-receptive MHC. It can be loaded with antigenic peptides matching HLA-G. Peptide ready MHC molecules comprising human HLA alleles and B2M, which can b... | |||
TMPK-01418 | Peptide Ready HLA-G&B2M Monomer Protein, Human, MHC (His & Avi) | Human | HEK293 |
Peptide Ready HLA-G&B2M Monomer is absent from peptide, namely peptide-receptive MHC. It can be loaded with antigenic peptides matching HLA-G. Peptide ready MHC molecules comprising human HLA alleles and B2M, which can b... |