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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T12116L | MSI-1701 | Others | |
MSI-1701 is an analogue of MSI-1436. | |||
T12116 | MSI-1436 | Aminosterol-1436,Trodusquemine | Others |
MSI-1436 is a selective, non-competitive the enzyme protein-tyrosine phosphatase 1B (PTB1B)inhibitor(IC50 of appr 1 μM) | |||
T12117 | MSI-1436 lactate | Trodusquemine lactate,Aminosterol-1436 lactate | Others |
MSI-1436 lactate is a selective, non-competitive the enzyme protein-tyrosine phosphatase 1B (PTB1B)inhibitor(IC50 of appr 1 μM) | |||
T12995 | Squalamine | MSI-1256 | Others |
Squalamine is an aminosterol compound, with potent broad spectrum antiviral activity. | |||
T12996 | Squalamine lactate | MSI-1256F | Others |
Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity. | |||
T16766 | Ro 08-2750 | ||
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 µM. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2... | |||
T2145 | Temsirolimus | NSC 683864,CCI-779 | Apoptosis , mTOR , Autophagy |
Temsirolimus (CCI-779) is a specific mTOR inhibitor ( IC50: 1.76 μM), used in the treatment of advanced renal cell cancer. | |||
T21314 | Amsilarotene | TAC-101,TAC 101,TAC101 | CDK |
Amsilarotene (TAC101) inhibits the phosphorylation of retinoblastoma gene product (RB) and increases the presence of 2 cyclin-dependent kinases (CDK) inhibitors resulting in cell cycle arrest. This agent also causes a cy... | |||
T69669 | Camsirubicin HCl | ||
Camsirubicin, also known as GPX-150, MNPR-201, and CNDO1011, is a synthetic non-cardiotoxic analogue of the anthracycline antibiotic doxorubicin with potential antineoplastic activity. Anthracycline analogue GPX-150 inte... | |||
T125382 | Extensumside F | ||
Extensumside F is a useful organic compound for research related to life sciences. The catalog number is T125382 and the CAS number is 2079912-12-0. | |||
T68811 | Trimetaphan camsilate | ||
Trimetaphan camsilate is a drug that counteracts cholinergic transmission at the ganglion type of nicotinic receptors of the autonomic ganglia and therefore blocks both the sympathetic nervous system and the parasympathe... | |||
T125381 | Extensumside H | ||
Extensumside H is a useful organic compound for research related to life sciences. The catalog number is T125381 and the CAS number is 2079912-14-2. | |||
T125383 | Extensumside E | ||
Extensumside E is a useful organic compound for research related to life sciences. The catalog number is T125383 and the CAS number is 2079912-11-9. | |||
T77032 | Imsidolimab | ||
Imsidolimab (ANB 019), a high-affinity, humanized monoclonal antibody targeting IL-36R, antagonizes IL-36 cytokine signal transduction, showing potential in treating generalized pustular psoriasis (GPP) and other inflamm... | |||
T77025 | Gimsilumab | ||
Gimsilumab (MORAb-022), a humanized anti-GM-CSF monoclonal antibody, shows promise in the research of COVID-19 and rheumatoid arthritis (RA) [1] [2]. | |||
T125384 | Extensumside C | ||
Extensumside C is a useful organic compound for research related to life sciences. The catalog number is T125384 and the CAS number is 2079912-09-5. | |||
T80548 | mSIRK | ERK | |
mSIRK (G-Protein βγ Binding Peptide) is a cell-permeable activator of ERK 1/2 with an EC50 of 2.5-5 μM. It disrupts the interaction between the α and βγ subunits, facilitating α subunit dissociation without inducing nucl... | |||
T25201 | Camsirubicin | ||
Camsirubicin is a drug candidate of antineoplastic. | |||
T73653 | Pexiganan | ||
Pexiganan (MSI 78 free base), a synthetic analog of magainin 2, is a potent, broad-spectrum antimicrobial peptide with oral activity. It is utilized in researching infections, including diabetic foot ulcer infections [1]... | |||
T72216 | DPM-1001 trihydrochloride | ||
DPM-1001 trihydrochloride, an analog of the specific protein-tyrosine phosphatase (PTP1B) inhibitor MSI-1436, is a potent, specific, non-competitive, orally active inhibitor of PTP1B with an IC50 of 100 nM, exhibiting an... |