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T79817S1P1 agonist 6 hemicalcium；化合物 S1P1 agonist 6 hemicalciumS1P1 agonist 6 hemicalcium
Compound I (S1P1 agonist 6 hemicalcium) is an S1P1 agonist that diminishes autoimmune activity by inhibiting lymphocyte trafficking, and serves as an immunosuppressive agent in researching a range of autoimmune diseases [1].
价 格：￥电议型 号：T79817产 地：中国大陆
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T79816S1P1 agonist 6；化合物 S1P1 agonist 6S1P1 agonist 6
Compound I (S1P1 agonist 6) is an S1P1 agonist that mitigates autoimmune activity by inhibiting lymphocyte trafficking and has potential as an immunosuppressive agent in autoimmune disease research [1].
价 格：￥电议型 号：T79816产 地：中国大陆
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T79815c-Fms-IN-14；化合物 c-Fms-IN-14c-Fms-IN-14
c-Fms-IN-14 (Example 76) is a potent inhibitor of the c-Fms kinase with an IC50 of 4 nM, utilized in cancer and autoimmune disease research [1].
价 格：￥电议型 号：T79815产 地：中国大陆
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T79814pan-KRAS-IN-3；化合物 pan-KRAS-IN-3pan-KRAS-IN-3
Pan-KRAS-IN-3 (Example 84) is a pan-KRAS inhibitor suitable for cancer research [1].
价 格：￥电议型 号：T79814产 地：中国大陆
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T79813Raf inhibitor 3；化合物 Raf inhibitor 3Raf inhibitor 3
Raf inhibitor 3 (Example 30), a potent inhibitor of both B-Raf and C-Raf, exhibits IC50 values below 15 nM. It is applicable in cancer research studies [1].
价 格：￥电议型 号：T79813产 地：中国大陆
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T79812BTK-IN-27；化合物 BTK-IN-27BTK-IN-27
BTK-IN-27 (example 8), a potent BTK inhibitor with an IC50 of 0.2 nM, demonstrates anti-proliferative effects in TMD8 cells with an IC50 of less than 5 nM. It is suitable for the research of various conditions including cancer, lymphoma, leukemia, and immunological diseases [1].
价 格：￥电议型 号：T79812产 地：中国大陆
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T79811DDR1/2 inhibitor-2；化合物 DDR1/2 inhibitor-2DDR1/2 inhibitor-2
DDR1/2 Inhibitor-2 (Example 31) serves as an inhibitor of DDR1/DDR2, exhibiting IC50 values below 100 nM. It is applicable in cancer and fibrotic disease research [1].
价 格：￥电议型 号：T79811产 地：中国大陆
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T79810Porcn-IN-2；化合物 Porcn-IN-2Porcn-IN-2
Porcn-IN-2 (Example 107) is a potent Wnt pathway inhibitor, exhibiting an IC50 of 0.05 nM. It has applications in cancer research, including sarcoma, melanoma, skin cancer, hematological tumors, lymphoma, carcinoma, and leukemia [1].
价 格：￥电议型 号：T79810产 地：中国大陆
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T79812-Fluoroadenosine；2-氟腺苷2-Fluoroadenosine
2-Fluoroadenosine is a potent inhibitor of lymphocyte-mediated cytolysis.
价 格：￥电议型 号：T7981产 地：中国大陆
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T78981Xeniafaraunol A；化合物 Xeniafaraunol AXeniafaraunol A
Xeniafaraunol A (compound 31) is a potent inhibitor of the transient receptor potential melastatin 7 (TRPM7) channel [1].
价 格：￥电议型 号：T78981产 地：中国大陆
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T77981Pomalidomide-5-C11-NH2 hydrochloride；化合物 Pomalidomide-5-C11-NH2 hydrochloridePomalidomide-5-C11-NH2
Pomalidomide-5-C11-NH2 hydrochloride is a Pomalidomide-derived cereblon (CRBN) ligand that facilitates the recruitment of the CRBN protein. This compound can be conjugated to a protein ligand via a linker to create a PROTAC [1].
价 格：￥电议型 号：T77981产 地：中国大陆
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T76981Tibulizumab；化合物 TibulizumabTibulizumab
Tibulizumab (LY 3090106), a tetravalent bispecific monoclonal antibody, selectively binds to B-cell activating factor (BAFF) and IL-17A with dissociation constants (Kd) of 60 pM and 14 pM, respectively. This specificity renders it a valuable tool for autoimmune disease research.
价 格：￥电议型 号：T76981产 地：中国大陆
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T76006Tirzepatide TFA；化合物 Tirzepatide TFATirzepatide TFA(2023788-19-2 free base)|||LY3298176 TFA；Tirzepati
Tirzepatide TFA (LY3298176 TFA), a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist, is under development for type 2 diabetes treatment [1].
价 格：￥电议型 号：T76006产 地：中国大陆
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T74981Transketolase-IN-3；化合物 Transketolase-IN-3Transketolase-IN-3
Transketolase-IN-3, a potent inhibitor of transketolase (TK), exhibits herbicidal activity by effectively suppressing Digitaria sanguinalis (DS) and Amaranthus retroflexus (AR). This compound holds potential for herbicide research applications [1].
价 格：￥电议型 号：T74981产 地：中国大陆
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T73981Deschloro Cetirizine dihydrochloride；化合物 Deschloro Cetirizine dihydrochlorideDeschloro Cetirizine di
Deschloro Cetirizine Dihydrochloride is an impurity of Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine. It functions as a specific, orally active, and long-acting histamine H1-receptor antagonist.
价 格：￥电议型 号：T73981产 地：中国大陆
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T71981Gliclazide-d4；化合物 Gliclazide-d4Gliclazide-d4
Gliclazide-d4 is intended for use as an internal standard for the quantification of gliclazide by GC- or LC-MS. Gliclazide is a sulfonylurea and an inhibitor of pancreatic β-cell ATP-sensitive potassium (KATP) channels. It is selective for pancreatic β-cell over cardiac and arterial smooth muscle cell KATP channels. Gliclazide (5 μM) increases insulin-induced glucose uptake and glucose transporter 4 (GLUT4) translocation to the plasma membrane in a differentiated 3T3L1 adipocyte model of insulin
价 格：￥电议型 号：T71981产 地：中国大陆
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T7189AMG9810化合物AMG9810(2E)-N-(2,3-二氢-1,4-苯并二噁英-6-基)-3-[4-(1,1-二甲基乙基)苯基]-2-丙酰胺
AMG 9810 is a competitive antagonist of capsaicin activation of the vanilloid receptor 1 (TRPV1) (IC50s = 24.5 and 85.6 nM for human and rat TRPV1, respectively).
价 格：￥电议型 号：T7189产 地：中国大陆
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T70981CGS 22745；化合物 CGS 22745CGS 22745
CGS 22745 is a selective orally active inhibitor of 5-lipoxygenase
价 格：￥电议型 号：T70981产 地：中国大陆
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T70747ICI-198157；化合物 ICI-198157ICI-198157
ICI-198157 is a selective beta3-adrenergic agonist of brown adipose tissue and thermogenesis in rat.
价 格：￥电议型 号：T70747产 地：中国大陆
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T69981CRM-51005；化合物 CRM-51005CRM-51005
CRM-51005 is a new phospholipase C inhibitor produced by unidentified fungal strain MT51005
价 格：￥电议型 号：T69981产 地：中国大陆
