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T60033SBI993SBI993
SBI993 is an analog of SBI-477 and can be used as a biomarker to confirm the expected action of MondoA target gene expression in vivo. SBI993 reduces muscle TAG levels and hepatic steatosis.
价 格：￥电议型 号：T60033产 地：中国大陆
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T22286Cyanosafracin Binhibit,Inhibitor,Cyanosafracin B
Cyanosafracin B is a compound which can be used in the synthesis of ecteinascidin ET-743 (an antitumor chemotherapy drug).
价 格：￥电议型 号：T22286产 地：中国大陆
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T60060ACSS2-IN-2
ACSS2-IN-2 is an inhibitor of acyl-CoA synthetase short-chain family member 2 (ACSS2). ACSS2-IN-2 can inhibit ACSS2 activity with an IC50 value of 3.8 nM. ACSS2-IN-2 can be used for the research of several diseases, such as viral infection, metabolic disorders, neuropsychiatric diseases, inflammatory/autoimmune conditions and cancer.
价 格：￥电议型 号：T60060产 地：中国大陆
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T6S0781PhellodendrineNuclear factor-kappaB,inhibit,Akt,Nuclear factor-κB,Inhibitor,PKB,Protein kinase B,NF-
1. Phellodendrine has anti-nephritic activity, may be due to its ability to inhibit the proliferation or the migration of macrophages and cytotoxic T lymphocytes in the glomeruli.
价 格：￥电议型 号：T6S0781产 地：中国大陆
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TN1563Dehydropachymic acidAutophagy,inhibit,Inhibitor,Dehydropachymic acid
Dehydropachymic acid shows antiinflammatory activity.
价 格：￥电议型 号：TN1563产 地：中国大陆
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T6370AEBSF hydrochlorideThrombin,Influenza Virus,AEBSF hydrochloride,AEBSF,Ser/Thr Protease,Threonine pro
AEBSF hydrochloride is an irreversible inhibitor of serine proteases, such as chymotrypsin, kallikrein, thrombin, plasmin, and trypsin.
价 格：￥电议型 号：T6370产 地：中国大陆
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TP1238LACTH 1-14 acetate(25696-21-3 free base)ACTH 1 14 acetate(25696 21 3 free base),ACTH 114 acetate(2569
ACTH (1-14) is a fragment of adrenocorticotrophin, which regulates cortisol and androgen production.Adrenocorticotropic hormone (ACTH), also known as corticotropin, is produced and secreted by the anterior pituitary gland. ACTH is an important component of the hypothalamic-pituitary-adrenal axis as a response to biological stress.
价 格：￥电议型 号：TP1238L产 地：中国大陆
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TQ0158AzaserineAntibiotic,Inhibitor,Bacterial,P165,CI 337,CI337,P 165,Azaserine,inhibit
Azaserine is a tumor-inhibiting antibiotic isolated from a species of Streptomyces and functions as an inhibitor of glutamine amidotransferase.
价 格：￥电议型 号：TQ0158产 地：中国大陆
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T12360para-Nitroblebbistatin
para-Nitroblebbistatin is a non-cytotoxic, fluorescent, photostable and specific Myosin II inhibitor. para-Nitroblebbistatin can be used in the study of the special role of myosin II in developmental, physiological,, and cell biological studies.
价 格：￥电议型 号：T12360产 地：中国大陆
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T60094SU 4981
SU 4981 is an inhibitor of VEGFR and a modulator of tyrosine kinase activity.
价 格：￥电议型 号：T60094产 地：中国大陆
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T6716ValsartanAngiotensin Receptor,Inhibitor,failure,blood,proinflammatory,aorta,CGP-48933,endothelial,cy
Valsartan is a tetrazole derivative and angiotensin II type 1 receptor blocker that is used to treat hypertension.
价 格：￥电议型 号：T6716产 地：中国大陆
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T61813AMPA receptor antagonist-3
AMPA receptor antagonist-3 is an AMPA receptor antagonist (patent US20070027143A1).
价 格：￥电议型 号：T61813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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T6S0923HypericinHypericin,Dopamine β-monooxygenase,antitumor activity,Antibiotic,antiviral activity,telomer
1. Hypericin has antineoplastic activity. 2. Hypericin has antibiotic and antiviral activities. 3. Hypericin has antidepressive activity through inhibiting monoamine oxidase enzyme. 4. Hypericin inhibits RANKL-mediated osteoclastogenesis via affecting ERK signalling in vitro and suppresses wear particle-induced osteolysis in vivo.
价 格：￥电议型 号：T6S0923产 地：中国大陆
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T9616PD-1/PD-L1-IN-10Lewis,T-lymphocyte,tumor,IFN-γ,Inhibitor,lung,LLC,inhibit,Apoptosis,PD1/PDL1IN10,PD
PD-1/PD-L1-IN-10 is an orally active?PD-1/PD-L1?inhibitor (IC50?of 2.7 nM) with potent anticancer efficacy.
价 格：￥电议型 号：T9616产 地：中国大陆
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T8767PfDHODH-IN-2malaria,Dihydroorotate Dehydrogenase,inhibit,PfDHODH,3D7,Inhibitor,Plasmodium falciparum
PfDHODH-IN-2 is a dihydrothiophenone derivative, is a potent Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH, IC50 : 1.11 μM) inhibitor . It is used an antimalarial agent and can be used for the research of malaria
价 格：￥电议型 号：T8767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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T16528PI-828
PI-828 is a phosphatidylinositol 3-kinase (PI3K) inhibitor, which is widely used to study the physiological function of PI3K and also promotes stem cell differentiation into mesoderm.
价 格：￥电议型 号：T16528产 地：中国大陆
