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T5516diABZI STING agonist-1 trihydrochloridediABZI STING agonist-1 trihydrochloride
diABZI STING agonist-1 (trihydrochloride) is stimulator of interferon genes (STING) receptor agonist.
价 格：￥电议型 号：T5516产 地：美洲
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T8649TMBIM6 antagonist-1；1-（2-氨基苯基）-3-（3-硝基苯基）-2-丙烯-1-酮BAX-inhibitor-1|||BIA；BAX-inhibitor-1|||1-（2-氨基苯基）
TMBIM6 antagonist-1 (BAX-inhibitor-1) is a bax inhibitor
价 格：￥电议型 号：T8649产 地：中国大陆
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T8328STING agonist-1；化合物STING agonist-1G10；G10
STING agonist-1 (G10) is a human-specific STING agonist,elicits antiviral activity against emerging Alphaviruses.
价 格：￥电议型 号：T8328产 地：中国大陆
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T82303Glucocorticoid receptor agonist-1 phosphate Gly-Glu TFA；化合物 Glucocorticoid receptor agonist-1 phosph
Glucocorticoid Receptor Agonist-1 Phosphate Gly-Glu (TFA) serves as a cleavable linker for the synthesis of Antibody-Drug Conjugates (ADCs).
价 格：￥电议型 号：T82303产 地：中国大陆
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T81803MFN2 agonist-1；化合物 MFN2 agonist-1MFN2 agonist-1
MFN2 agonist-1 (B-A/l) effectively induces mitochondrial fusion in cells deficient in mitofusin 2 (MFN2). It counteracts mitochondrial "clumping" (formation of static mitochondrial aggregates) and reinstates mitochondrial movement in cultured mouse neurons harboring the CMT2A-associated MFN2 T105M mutation.
价 格：￥电议型 号：T81803产 地：中国大陆
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T81801mGluR5 antagonist-1；化合物 mGluR5 antagonist-1mGluR5 antagonist-1
mGluR5 antagonist-1 (compound 10) is a potent mGluR5 inhibitor exhibiting an IC50 of 11.5 nM and demonstrates antidepressant effects [1].
价 格：￥电议型 号：T81801产 地：中国大陆
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T81246RXFP1 receptor agonist-1；化合物 RXFP1 receptor agonist-1RXFP1 receptor agonist-1
RXFP1 receptor agonist-1 (Example 2), an agonist of the RXFP1 receptor, suppresses cAMP production in HEK293 cells that constitutively express the human RXFP1, exhibiting an EC50 of 300 nM [1].
价 格：￥电议型 号：T81246产 地：中国大陆
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T81084STING agonist-18；化合物 STING agonist-18STING agonist-18
STING Agonist-18 (Compound 1a) is a precursor for the synthesis of antibody-drug conjugates (ADCs), including Trastuzumab conjugates [1].
价 格：￥电议型 号：T81084产 地：中国大陆
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T81083STING agonist-19；化合物 STING agonist-19STING agonist-19
STING agonist-19 serves as a precursor for the synthesis of immune-stimulating antibody conjugates (ISACs).
价 格：￥电议型 号：T81083产 地：中国大陆
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T81040TAS2R14 agonist-1；化合物 TAS2R14 agonist-1TAS2R14 agonist-1
TAS2R14 agonist is a potent partial agonist of TAS2R14, displaying an EC50 value of 116.6 ± 23.6 nM [1].
价 格：￥电议型 号：T81040产 地：中国大陆
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T80978TLR4 agonist-1；化合物 TLR4 agonist-1TLR4 agonist-1
TLR4 agonist-1 (compound 17a) serves as a potent activator of Toll-like Receptor 4 (TLR4) and stimulates the production of MIP-1β in RAW 264.7 and MM6 cells [1].
价 格：￥电议型 号：T80978产 地：中国大陆
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T80977TLR4 agonist-1 TEA；化合物 TLR4 agonist-1 TEATLR4 agonist-1 TEA
TLR4 agonist-1 (TEA, compound 17a) is a potent activator of Toll-like Receptor 4 (TLR4) and prompts the production of MIP-1β in RAW 264.7 and MM6 cells [1].
价 格：￥电议型 号：T80977产 地：中国大陆
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T80758Y4R agonist-1；化合物 Y4R agonist-1Y4R agonist-1
Y4R Agonist-1 is a potent agonist of the Y4 receptor, exhibiting a K_i (inhibition constant) value of 0.048 nM.
价 格：￥电议型 号：T80758产 地：中国大陆
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T798065-HT2A&5-HT2C agonist-1；化合物 5-HT2A&5-HT2C agonist-15-HT2A&5-HT2C agonist-1
5-HT2A&5-HT2C agonist-1 (Example 2) is a dual-acting agent targeting the 5-HT2A and 5-HT2C receptors with respective IC50 values of 196 nM and 0.9 nM. It is applicable in the study of various central nervous system disorders including depression, alcoholism, tobacco and cocaine addiction, inflammation, cluster headaches, post-traumatic stress disorder (PTSD), and seizure disorders [1].
价 格：￥电议型 号：T79806产 地：中国大陆
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T798055-HT2 agonist-1 free base；化合物 5-HT2 agonist-1 free base5-HT2 agonist-1 free base
Compound 24 (5-HT2 agonist-1 free base) is a potent agonist for 5-HT2A, 5-HT2B, and 5-HT2C receptors, exhibiting IC50 values of 10 nM, 8.3 nM, and 1.6 nM, respectively. It is utilized in research pertaining to depression, alcoholism, tobacco and cocaine addiction, inflammation, cluster headache, PTSD, seizure disorders, and other central nervous system disorders. [1]
价 格：￥电议型 号：T79805产 地：中国大陆
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T798045-HT2 agonist-1；化合物 5-HT2 agonist-15-HT2 agonist-1
Compound 24, a 5-HT2 agonist-1, selectively activates 5-HT2A, 5-HT2B, and 5-HT2C receptors with IC50 values of 10 nM, 8.3 nM, and 1.6 nM, respectively. The free base form of this compound is utilized in research pertaining to depression, alcoholism, tobacco and cocaine addiction, inflammation, cluster headaches, PTSD, seizure disorders, and additional CNS disorders [1].
价 格：￥电议型 号：T79804产 地：中国大陆
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T79793CRF1 receptor antagonist-1；化合物 CRF1 receptor antagonist-1CRF1 receptor antagonist-1
CRF1 Receptor Antagonist-1 (Compound 2), a CRF1 receptor antagonist, is utilized in research pertaining to congenital adrenal hyperplasia (CAH) [1].
价 格：￥电议型 号：T79793产 地：中国大陆
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T79418BLT2 antagonist-1；化合物 BLT2 antagonist-1BLT2 antagonist-1
BLT2 antagonist-1 (compound 15b) is a selective inhibitor of the BLT2 receptor, impeding the chemotaxis of CHO-BLT2 cells at an IC50 of 224 nM, while not affecting CHO-BLT1 cell chemotaxis. It blocks the interaction between LTB4 and the BLT2 receptor with a K_i of 132 nM and may serve as a research tool for inflammatory airway diseases, including asthma and chronic obstructive pulmonary disease [1].
价 格：￥电议型 号：T79418产 地：中国大陆
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T79071HPK1 antagonist-1；化合物 HPK1 antagonist-1HPK1 antagonist-1
HPK1 antagonist-1 (I-792) is an inhibitor targeting HPK1, with potential applications in cancer and immune disease research [1].
价 格：￥电议型 号：T79071产 地：中国大陆
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T79066THRβ receptor agonist-1；化合物 THRβ receptor agonist-1THRβ receptor agonist-1
THRβ receptor agonist-1 is an agonist for the THRβ receptor [1].
价 格：￥电议型 号：T79066产 地：中国大陆
