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Caspase

Caspase

Caspase related products

Structure Cat No. Product Name CAS No. Product Description
Ac-DMLD-CMK V128076 Ac-DMLD-CMK 2588354-33-8 Ac-DMLD-CMK is a caspase 3 inhibitor and a GSDME inhibitor.
Ac-VDVAD-CHO TFA V128272 Ac-VDVAD-CHO TFA Ac-VDVAD-CHO TFA is a caspase-2/3 inhibitor (IC50: 46 and 15 nM).
ATWLPPRAANLLMAAS V106281 ATWLPPRAANLLMAAS 1228447-26-4 ATWLPPRAANLLMAAS is a chimeric peptide with anti-angiogenic and potent anti-tumor effects.
Boc-AEVD-CHO TFA V112049 Boc-AEVD-CHO TFA Boc-AEVD-CHO TFA is a caspase 8 inhibitor.
Caspase-3-IN-3 V131116 Caspase-3-IN-3 1984421-81-9 Caspase-3-IN-3 is a caspase 3 inhibitor.
CDK6-IN-2 V131291 CDK6-IN-2 CDK6-IN-2 is a CDK6 covalent inhibitor with an IC50 value of 0.013 μM.
Estrogen receptor modulator 10 V67696 Estrogen receptor modulator 10 2991504-90-4 Estrogen receptor modulator 10 (compound G-5b) is an estrogen receptor (ER) antagonist (IC50=6.7 nM) and degrader (DC50=0.4 nM).
HDAC-IN-82 V104867 HDAC-IN-82 HDAC-IN-82 (compound 18b) is a histone deacetylase (HDAC) inhibitor with selective anti-plasmodial and anti-cancer activities.
HDAC1/6-IN-3 V137173 HDAC1/6-IN-3 3038691-85-6 HDAC1/6-IN-3 is a potent HDAC inhibitor.
IGN523 V120042 IGN523 IGN523 is an anti-CD98 antibody (hCD98, KD = 0.55 nM).
KEA1-97 V23175 KEA1-97 2138882-71-8 KEA1-97 is a selective Thioredoxin-caspase 3 interaction interferer (IC50=10 μM).
MO-2097 V140098 MO-2097 2744300-63-6 MO-2097 is a RAF-1/HIF-1α inhibitor.
N-(2-喹啉基)缬氨酰-天门冬氨酰-(2,6-二氟苯氧基)甲基酮 V0031 Q-VD-OPh 1135695-98-5 Q-VD-OPh (also known asQVD-OPH; Quinoline-Val-Asp-Difluorophenoxymethylketone) is a novel, potent and irreversiblepan-caspase inhibitor with potential anticancer activities.
RN-0001 V144231 RN-0001 252731-57-0 RN-0001 is a cycloavidin (Cyp) inhibitor with Ki values of 4.1 nM and 12.0 nM for CypA and CypD, respectively, and an EC50 value of 916 nM for CypD.
RP-182 acetate V144377 RP-182 acetate RP-182 acetate is a synthetic immunomodulatory peptide that exerts its antitumor effect by targeting the mannose receptor CD206 (Kd = 8 μM) on the surface of tumor-associated macrophages (TAMs).
SBP-5147 V144661 SBP-5147 1884222-37-0 SBP-5147 is an orally effective ULK1/ULK2 inhibitor with an IC50 of 2 nM for ULK1 and 53 nM for ULK2.
SL-176 V145021 SL-176 1809556-48-6 SL-176 is a PPM1D (Wip1) inhibitor.
SMO-IN-6 V145067 SMO-IN-6 SMO-IN-6 is a smoothed (SMO) inhibitor with an IC50 value of 0.12 μM in humans. It has enhanced water solubility, good plasma and metabolic stability, moderate therapeutic index, preliminary safety profile, and moderate oral bioavailability in rats.
SRSF1-IN-1 V145259 SRSF1-IN-1 SRSF1-IN-1 is an SRSF1 inhibitor.
STAT3-IN-44 V145296 STAT3-IN-44 STAT3-IN-44 is a potent STAT3 inhibitor with IC50 values of 1.84 μM (C6 cells) and 4.81 μM (A549 cells).
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