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T38343Quercetin pentaacetatePentaacetylquercetin
Quercetin pentaacetate has diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties. Quercetin pentaacetate interacts with RSV and inhibit the viral adhesion on cell surface.
价 格：￥电议型 号：T38343产 地：中国大陆
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T37434-hydroxyphenylacetic acidp-Hydroxyphenylacetic acid；parahydroxy phenylacetate；4-羟基苯乙酸；对羟基苯乙酸
4-hydroxyphenylacetic acid, a major microbiota-derived metabolite of polyphenols, is involved in the antioxidative action. 4-hydroxyphenylacetic acid induces expression of Nrf2.
价 格：￥电议型 号：T3743产 地：中国大陆
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T3715AcebilustatCTX-4430；阿西鲁司特
Acebilustat (ZK322) is an effective and specific leukotriene B4 hydrolase inhibitor.
价 格：￥电议型 号：T3715产 地：中国大陆
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T3643HMN-176HMN 176；HMN176
HMN-176 is a stilbene derivative which inhibits mitosis, interfering with polo-like kinase-1 (plk1).
价 格：￥电议型 号：T3643产 地：中国大陆
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T3632DoravirineMK-1439；多拉维林；多拉韦林
Doravirine is a non-nucleoside reverse transcriptase inhibitor, used in the treatment of HIV/AIDS.
价 格：￥电议型 号：T3632产 地：中国大陆
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T3582BTZ043
BTZ043 is a DprE1 inhibitor with nanomolar bactericidal activity against Mycobacterium tuberculosis in vitro.
价 格：￥电议型 号：T3582产 地：中国大陆
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T3570SU4312NSC 86429；SU 4312
SU-4312, also known as DMBI, is a potent and selective inhibitor of VEGFR and PDGFR tyrosine kinases (IC50 values are 0.8 and 19.4 μM respectively). SU4312 unexpectedly protects against MPP(+) -induced neurotoxicity via selective and direct inhibition of
价 格：￥电议型 号：T3570产 地：中国大陆
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T3548Epacadostat艾卡哚司他；INCB 024360；IDO Inhibitor 1
Epacadostat is an oral-available inhibitor of indoleamine 2, 3-dioxygenase (IDO1), increasing the proliferation and activation of various immune cells and reducing tumor-associated regulatory T cells.
价 格：￥电议型 号：T3548产 地：中国大陆
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T35343MTI-31MTI-31；LXI-15029
MTI-31 is a potent, orally active and highly selective inhibitor of mTORC1 and mTORC2. MTI-31 is selective for mTOR (Kd: 0.20 nM) versus PIK3CA, PIK3CB and PIK3G with >5,000 fold selectivity in mTOR binding assays. MTI-31 shows an IC50 of 39 nM for mTOR i
价 格：￥电议型 号：T35343产 地：中国大陆
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T3528Senicapoc塞尼卡泊；ICA-17043
Senicapoc is a potent inhibitor of the Gardos channel and ameliorates RBC dehydration in the SAD mouse. Senicapoc blocked Ca2+-induced rubidium flux from human RBCs with an IC50 value of 11 ± 2 nM (CLT IC50 = 100 ± 12 nM) and inhibited RBC dehydration wit
价 格：￥电议型 号：T3528产 地：中国大陆
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T3474RO 46-8443
RO 46-8443 is the first non-peptide endothelin ETB receptor selective antagonist. RO 46-8443 displays up to 2000-fold selectivity for ETB receptors both in terms of binding inhibitory potency and functional inhibition.
价 格：￥电议型 号：T3474产 地：中国大陆
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T3443ArgiprestocinArginine vasotocin；精氨缩宫素
Vasopressin, also called antidiuretic hormone that plays a key role in maintaining osmolality. It is a neurohypophysial hormone found in most mammals. Drugs used to cause constriction of the blood vessels.
价 格：￥电议型 号：T3443产 地：中国大陆
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T3439ML348GNF-Pf-1127
ML348 is a selective and reversible lysophospholipase 1 (LYPLA1) inhibitor (IC50 = 210 nM).
价 格：￥电议型 号：T3439产 地：中国大陆
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T3438S107
S107 is a RyR-selective 1, 4-benzothiazepine derivative that stabilizes RyR2 channels by enhancing the binding affinity of calstabin2 to mutant and/or PKA-phosphorylated channels.
价 格：￥电议型 号：T3438产 地：中国大陆
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T3437Lys05Lys01 trihydrochloride
Lys05, or Lys01 trihydrochloride, is a potent, water soluble lysosomal autophagy inhibitor. Lys05 is a previously undescribed dimeric chloroquine which more potently accumulates in the lysosome and blocks autophagy compared with HCQ. Lys05 produced more p
价 格：￥电议型 号：T3437产 地：中国大陆
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T3436LYS01lys05 (free base)
LYS01 free base is a new lysosomal autophagy inhibitor.
价 格：￥电议型 号：T3436产 地：中国大陆
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T3435Vicriviroc maleateSCH-D (maleate)；SCH-417690 (maleate)；维立韦罗马来酸盐
Vicriviroc maleate(Sch-417690) is a piperazine-based CCR5 receptor antagonist with activity against human immunodeficiency virus. The IC50 value is 0.91 nM in clinical development for the treatment of HIV-1.
价 格：￥电议型 号：T3435产 地：中国大陆
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T3433TUG-891TUG 891；TUG891
TUG-891 is a G protein-coupled receptor (GPCR) expressed in intestine, adipocytes, and pro-inflammatory macrophages that is activated by long chain free fatty acids.
价 格：￥电议型 号：T3433产 地：中国大陆
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T3432Cinobufagin华蟾蜍精；华蟾酥毒基；Cinobufagine
Cinobufagin is a selective Na+/K+-ATPase inhibitor. The activity of Cinobufagin is same as ouabain.
价 格：￥电议型 号：T3432产 地：中国大陆
