
Inhibidores
Subcategorías de "Inhibidores"
- Angiogénesis(2.797 productos)
- Apoptosis(6.257 productos)
- Ciclo celular / Checkpoint(4.836 productos)
- Cromatina / Epigenética(2.592 productos)
- Señalización citoesquelética(1.534 productos)
- Daño al ADN / Reparación del ADN(2.880 productos)
- Endocrinología / Hormonas(3.748 productos)
- Enzima(3.670 productos)
- GPCR / proteína G(8.985 productos)
- Inmunología e inflamación(3.794 productos)
- Virus de la gripe(299 productos)
- Señalización JAK / STAT(415 productos)
- Señalización MAPK(1.250 productos)
- Transportador de membrana / canal de iones(3.148 productos)
- Metabolismo(10.144 productos)
- Microbiología / Virología(7.591 productos)
- Neurociencia(10.345 productos)
- Otros inhibidores(35.829 productos)
- Reducción de oxidación(40 productos)
- Señalización PI3K / Akt / mTOR(1.421 productos)
- Proteasas / Proteasoma(1.680 productos)
- Células madre y Derivados(748 productos)
- Tirosina quinasa / adaptadores(1.960 productos)
- Ubiquitinación(1.721 productos)
Se han encontrado 66564 productos de "Inhibidores"
BPH-675
CAS:BPH-675 is a bioactive chemical.Fórmula:C24H23NO9P2SForma y color:SolidPeso molecular:563.45Questiomycin A derivatives 20
Questiomycin A derivatives 20 is a Questiomycin A derivative.
Fórmula:C15H12N2O4Pureza:99.94%Forma y color:SoildPeso molecular:284.27AS-604850
AS-604850: PI3Kγ inhibitor, ATP-competitive, IC50=2.5μM, 30x> PI3Kδ/β, 18x> PI3Kα.
Fórmula:C11H5F2NO4SPureza:98%Forma y color:SolidPeso molecular:285.22N2S2-CBMBC
CAS:N2S2-CBMBC, a bromo-benzyl ether, binds to 99mTc for PD-L1 tumor imaging, offering a real-time alternative to immunohistochemistry.
Fórmula:C34H33BrClN3O3S2Forma y color:SolidPeso molecular:711.13DAUDA
CAS:DAUDA (11-(dansylamino)undecanoic acid), an environment-sensitive fluorescent fatty acid analogue, exhibits changes in fluorescent emission spectra andFórmula:C23H34N2O4SForma y color:SolidPeso molecular:434.59α-Conotoxin GI
CAS:α-conotoxin GI, a conopeptide isolated from the venom of the cone snail Conus geographus, is a competitive antagonist of the muscle-type nicotinic acetylcholine
Fórmula:C55H80N20O18S4Pureza:98%Forma y color:SolidPeso molecular:1437.61Thalidomide-NH-PEG4-Ms
CAS:Thalidomide-NH-PEG4-Ms: cereblon ligand + linker, for PROTAC BCL-XL degrader XZ739.
Fórmula:C22H29N3O10SForma y color:SolidPeso molecular:527.551,6,8-Trihydroxy-2,7-dimethoxy-3-methylanthraquinone
1,6,8-Trihydroxy-2,7-dimethoxy-3-methylanthraquinone is a useful organic compound for research related to life sciences and the catalog number is T125250.
Fórmula:C34H26O14Forma y color:SolidPeso molecular:658.568MCAAD-3
CAS:MCAAD-3, a near-infrared Aβ imaging probe, exhibits blood-brain barrier permeability and strong affinity for Aβ polymers (Ki >106 nM).
Fórmula:C17H18N2O2Forma y color:SolidPeso molecular:282.34Antibiotic K 4
CAS:Antibiotic K 4 is an inhibitor of angiotensin I converting enzyme produced by Actinomadura spiculosospora.Fórmula:C23H32N3O6PPureza:98%Forma y color:SolidPeso molecular:477.498LCMV gp33-41 (TFA) (151705-84-9 free base)
LCMV gp33-41 (TFA) is an 11-aa peptide, MHC class I H-2Db-bound, presented to CTLs.Fórmula:C50H74N11F3015SPureza:98%Forma y color:SolidPeso molecular:1158.24PROTAC MDM2 Degrader-2
CAS:PROTAC MDM2 Degrader-2: A potent MDM2-targeting compound with PROTAC tech for E3 ligase-mediated degradation.
Fórmula:C70H76Cl4N10O12Pureza:98%Forma y color:SolidPeso molecular:1391.22SIAIS117
CAS:SIAIS117: A Brigatinib-VHL-1 ALK PROTAC; degrades ALK G1202R, inhibits SR/H2228 cells, may fight small cell lung cancer.
Fórmula:C57H76ClN10O7PSForma y color:SolidPeso molecular:1111.77(D)-PPA 1
CAS:PD-1/PD-L1 binder, Kd 0.51 μM; blocks interaction in flow cytometry at 1 mg/mL; inhibits tumors, extends mouse survival.
Fórmula:C70H98N20O21Pureza:98%Forma y color:SolidPeso molecular:1555.67KHS 101 hydrochloride (1262770-73-9 free base)
KHS 101 hydrochloride is a neuronal differentiation inducer
Fórmula:C18H21N5S·HClPureza:98%Forma y color:SolidPeso molecular:375.92MRS2802
CAS:MRS2802 is a P2Y14 receptor agonist, its EC50 value for P2Y14 receptor is 63 nM.Fórmula:C10H14F2N2O11P2Pureza:98%Forma y color:SolidPeso molecular:438.169CAY10735
CAS:CAY10735: Anticancer agent; inhibits growth/migration in various cancer cells; reduces tumor in mouse models. IC50=0.674-11.56μM.
Fórmula:C44H60FN3O4Forma y color:SolidPeso molecular:713.979PROTAC BRD4 Degrader-16
CAS:PROTAC BRD4 Degrader-16 is a potent degrader of BRD4, exhibiting IC50 values of 34.58 nM for BRD4 (BD1) and 40.23 nM for BRD4 (BD2).
Fórmula:C46H41N7O8Pureza:98%Forma y color:SolidPeso molecular:819.86PROTAC MDM2 Degrader-4
CAS:PROTAC MDM2 Degrader-4 targets MDM2 for degradation with E3 ligase via a linked inhibitor.
Fórmula:C70H74Cl4N8O14Pureza:98%Forma y color:SolidPeso molecular:1393.19

