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T39214LLXE408 fumarate
LXE408 fumarate is an orally active, non-competitive and kinetoplastid-selective?proteasome?inhibitor. LXE408 fumarate has an?IC50?of 0.04 μM for?L. donovani?proteasome and an?EC50?of 0.04 μM for?L. donovani. LXE408 fumarate has a low propensity to cross the blood brain barrier. LXE408 fumarate has the potential for visceral leishmaniasis (VL) research.
价 格：￥电议型 号：T39214L产 地：中国大陆
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T8480Tenovin-6 Hydrochlorideacetylation,Dihydroorotate Dehydrogenase,protein-deacetylating,Tenovin 6 Hydr
Tenovin-6 Hydrochloride is an SIRT1, SIRT2 and HDAC8 inhibitor(IC50s of 21 μM, 10 μM, and 67 μM for SirT1, SirT2, and SirT3, respectively), and is also a potent p53 activator .
价 格：￥电议型 号：T8480产 地：中国大陆
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TP2106LUrantide acetate(669089-53-6 free base)Urantide acetate(669089536 free base),Urantide acetate(669089
Urantide acetate is a selective and competitive urotensin-II (UT) receptor antagonist (pKB = 8.3). Blocks hU-II induced contractions in thoracic aorta ex vivo. Exhibits no effect on noradrenaline or endothelin 1-induced contraction or on acetylcholine-induced relaxation. Behaves as a partial agonist in a calcium mobilization assay (in CHO cells expressing hUT receptors).
价 格：￥电议型 号：TP2106L产 地：中国大陆
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T9703LGSK778 hydrochlorideGSK778 hydrochloride
GSK778 hydrochloride hydrochloride is a potent and selective BD1 bromodomain inhibitor of the BET proteins, with IC50s of 75 nM (BRD2 BD1), 41 nM (BRD3 BD1), 41 nM (BRD4 BD1), and 143 nM (BRDT BD1), respectively. GSK778 hydrochloride hydrochloride phenocopies the effects of pan-BET inhibitors in cancer models[1].
价 格：￥电议型 号：T9703L产 地：中国大陆
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TN1259Complanatoside BAnti-Inflammatory,inhibit,Inhibitor,Complanatoside B,flavonoid
Complanatoside B is a natural product
价 格：￥电议型 号：TN1259产 地：中国大陆
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T20797NE-100 hydrochloride?NE100 hydrochloride?,NE100,inhibit,Inhibitor,NE 100 hydrochloride?,Sigma Recept
NE100 HCl is a potent and selective antagonist of σ1 (IC50 = 4.16 nM) with antipsychotic activity. NE100 HCl also suppresses ER stress-induced hippocampal cell death.
价 格：￥电议型 号：T20797产 地：中国大陆
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T63049CHD1Li 6.11
CHD1Li 6.11 is a potent oncogenic CHD1L inhibitor. CHD1Li 6.11 exhibits IC50 of 3.3 ?M for cat-CHD1L recombinant protein. CHD1Li 6.11 is an orally bioavailable antitumor agent. CHD1Li 6.11 significantly reduces the tumor volume of CRC xenografts, which is generated from isolated quasi mesenchymal cells (M-phenotype).
价 格：￥电议型 号：T63049产 地：中国大陆
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T60095CCF0058981CCF0058981
CCF0058981 (CCF981) is a 3-chlorophenyl analogue which is a noncovalent SARS-CoV-2 3CL pro (SC2) inhibitor with an IC 50 of 68 nM. CCF0058981 inhibits SC1 (SARS-CoV-1 3CL pro ) with an IC 50 of 19 nM. CCF0058981 has antiviral efficacy and has the potential for COVID-19 research [1].
价 格：￥电议型 号：T60095产 地：中国大陆
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T15457LH-Lys-Trp-Lys-OH acetateH Lys Trp Lys OH acetate,HLysTrpLysOH acetate
H-Lys-Trp-Lys-OH acetate is a peptide with antibacterial and antiviral activities.
价 格：￥电议型 号：T15457L产 地：中国大陆
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T13303Virginiamycin M1
Virginiamycin M1 is a macrocyclic lactone peptide antibiotic and is a member of the streptogramin A group of antibiotics.
价 格：￥电议型 号：T13303产 地：中国大陆
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T9787suvn-911nicotinic,antidepressant,nAChR,acetylcholine,neuronal,Inhibitor,SUVN-911,suvn911,suvn 911,de
suvn-911 is a potent and selective antagonist of neuronal nicotinic acetylcholine α4β2 receptor (Ki = 1.5 nM) with antidepressant activity.
价 格：￥电议型 号：T9787产 地：中国大陆
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T6445CilomilastCilomilast,asthma,immunomodulatory,obstructive,Inhibitor,Phosphodiesterase (PDE),inhibit,P
Cilomilast is a potent PDE4 inhibitor with IC50 of about 110 nM, has anti-inflammatory activity and low central nervous system activity. Phase 3.
价 格：￥电议型 号：T6445产 地：中国大陆
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TN6088tricoumaroyl spermidinetricoumaroyl spermidine
Tricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.
价 格：￥电议型 号：TN6088产 地：中国大陆
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TP2482LCKLSL acetateLCKLSL acetate
LCKLSL acetate is a competitive annexin A2 (AnxA2) inhibitor. LCKLSL acetate potently inhibits the binding of tissue plasminogen activator (tPA) to AnxA2 and the generation of plasmin. LCKLSL acetate has anti-angiogenic roles.
价 格：￥电议型 号：TP2482产 地：中国大陆
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T10003α1 adrenoceptor-MO-1α1 adrenoceptor MO 1,α1 adrenoceptorMO1
α1 adrenoceptor-MO-1 (S enantiomer) has affinity at alpha 1 adrenergic receptor with alphalytic activity and analgesic action. It has more active than R enantiomer.
价 格：￥电议型 号：T10003产 地：中国大陆
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TN7118Methylhippuric acid
Methylhippuric acid is a xylene exposure biomarker in human urine.
价 格：￥电议型 号：TN7118产 地：中国大陆
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T7761Pomalidomide-C2-NH2 hydrochloridePomalidomideC2NH2 hydrochloride,inhibit,Inhibitor,Pomalidomide-C-2-
Pomalidomide-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate. Pomalidomide-C2-NH2 hydrochloride incorporates the Pomalidomide based cereblon ligand and a linker used in PROTAC technology.
价 格：￥电议型 号：T7761产 地：中国大陆
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T6461Dapoxetine hydrochlorideBenign,BPH,serotonin reuptake,SERT,sexual disorder,LY210448,SLC6A4,Dapoxetin
Dapoxetine HCl is a selectivity short-acting serotonin reuptake inhibitor, used for the therapy of premature ejaculation.
价 格：￥电议型 号：T6461产 地：中国大陆
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TP1057LPhe-Met-Arg-Phe Like Peptide acetatePheMetArgPhe Like Peptide acetate,Phe Met Arg Phe Like Peptide a
Phe-Met-Arg-Phe Like Peptide acetate is a FMRF-like peptide from visceral and somatic muscles of the snail Helix aspersa. FMRF (Phe-Met-Arg-Phe) is a neuropeptide peptide consisting of 4 amino acid residues.
价 格：￥电议型 号：TP1057L产 地：中国大陆
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T0030LBupivacaine
Bupivacaine is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.
价 格：￥电议型 号：T0030L产 地：中国大陆
