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T81156Sikokianin E；化合物 Sikokianin ESikokianin E
Sikokianin E, a biflavonone derivative, is isolable from Coreopsis tinctoria [1].
价 格：￥电议型 号：T81156产 地：中国大陆
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T81155Simridarlimab；化合物 SimridarlimabSimridarlimab
Simlukafusp alfa (Simridarlimab) is a humanized immunoglobulin antibody that targets the CD274/PD-L1 and CD47 pathways.[1]
价 格：￥电议型 号：T81155产 地：中国大陆
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T81154SIRT1 activator 1；化合物 SIRT1 activator 1SIRT1 activator 1
SIRT1 Activator 1 (Compound 3), a marine-derived xyloallenoide A derivative from the Xylaria sp. mangrove fungus, exhibits angiogenic effects in zebrafish and protects human endothelial progenitor cells (hEPCs) from AngII-induced senescence. It achieves this by elevating SIRT1 expression and modulating the AMPK/Akt signaling pathway [1].
价 格：￥电议型 号：T81154产 地：中国大陆
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T81153Sitakisogenin；化合物 SitakisogeninSitakisogenin
Sure, please provide the description of the chemical compound you´d like to be rewritten.
价 格：￥电议型 号：T81153产 地：中国大陆
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T81152SKF 81297；化合物 SKF 81297SKF 81297
SKF 81297 is a selective and potent agonist for the dopamine D1 receptor [1].
价 格：￥电议型 号：T81152产 地：中国大陆
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T81151SK-MLCK M13；化合物 SK-MLCK M13SK-MLCK M13
SK-MLCK M13 is a biologically active peptide representing the calmodulin (CaM)-binding domain of CaM target proteins, where CaM is a ubiquitous Ca2+ binding protein.
价 格：￥电议型 号：T81151产 地：中国大陆
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T81150SLSLSPG；化合物 SLSLSPGSLSLSPG
SLSLSPG, a common variant in immunoglobulin G (IgG) [1], is derived from the C-terminal end of the heavy chain of human Igγ-1.
价 格：￥电议型 号：T81150产 地：中国大陆
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T81149SMA4；化合物 SMA4SMA4
SMA4, a selective activator of PKG1α, exhibits a basal EC50 of 29 μM, enhances phosphorylation of the PKG1 substrate VASP, and inhibits proliferation of hPASMCs. It is utilized in cardiovascular disease research [1].
价 格：￥电议型 号：T81149产 地：中国大陆
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T81148Smac-based peptide；化合物 Smac-based peptideSmac-based peptide
Smac-based peptide, a biologically active peptide derived from SMAC that interacts with the BIR3 domain, exhibits specific biological functions.
价 格：￥电议型 号：T81148产 地：中国大陆
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T81147SMD-3040 TFA；化合物 SMD-3040 TFASMD-3040 TFA
SMD-3040 TFA is a selective SMARCA2 degrader comprising SMARCA2/4 ligands, a linker, and VHL ligands, utilized in PROTAC drug synthesis. It demonstrates robust tumor growth inhibition in tumor xenograft models [1].
价 格：￥电议型 号：T81147产 地：中国大陆
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T81146SMP-33693；化合物 SMP-33693SMP-33693
SMP-33693 is an Antibody-Drug Conjugate (ADC) known for its low payload shedding rate and demonstrated in vivo tumor inhibition in ovarian, gastric, and breast cancers [1].
价 格：￥电议型 号：T81146产 地：中国大陆
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T81145SMP-88480；化合物 SMP-88480SMP-88480
SMP-88480, an Antibody-Drug Conjugate (ADC), demonstrates stability in mouse, monkey, and human plasma, and exhibits in vivo tumor inhibitory effects on ovarian, gastric, and breast cancers [1].
价 格：￥电议型 号：T81145产 地：中国大陆
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T81144SMP-93566；化合物 SMP-93566SMP-93566
SMP-93566 is an antibody-drug conjugate (ADC) characterized by a low payload shedding rate, demonstrating in vivo tumor suppression in ovarian, gastric, and breast cancers [1].
价 格：￥电议型 号：T81144产 地：中国大陆
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T81143SN38-PAB-Lys(MMT)-oxydiacetamide-PEG8-N3；化合物 SN38-PAB-Lys(MMT)-oxydiacetamide-PEG8-N3SN38-PAB-Lys(MM
"SN38-PAB-Lys(MMT)-oxydiacetamide-PEG8-N3 is a drug-linker conjugate for antibody-drug conjugates (ADCs), consisting of the anti-cancer agent SN38 linked to Lys(MMT)-PAB-oxydiacetamide-PEG8-N3. It serves as a click chemistry reagent featuring an azide group that participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with alkyne-bearing molecules and can also engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with compounds containing DBCO or BCN groups, facilitating t
价 格：￥电议型 号：T81143产 地：中国大陆
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T81142SNIPER(TACC3)-1 hydrochloride；化合物 SNIPER(TACC3)-1 hydrochlorideSNIPER(TACC3)-1 hydrochloride
SNIPERTACC3-1 hydrochloride, an IAP ligand-based compound, selectively degrades the TACC3 protein through the ubiquitin-proteasome pathway, thereby inducing cancer cell apoptosis [1].
价 格：￥电议型 号：T81142产 地：中国大陆
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T81141SNIPER(TACC3)-2 hydrochloride；化合物 SNIPER(TACC3)-2 hydrochlorideSNIPER(TACC3)-2 hydrochloride
SNIPER(TACC3)-2 hydrochloride is a compound that induces degradation of the TACC3 protein through the ubiquitin-proteasome pathway by exploiting an IAP ligand, leading to the induction of cancer cell death [1].
价 格：￥电议型 号：T81141产 地：中国大陆
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T81140SNM1A-IN-1；化合物 SNM1A-IN-1SNM1A-IN-1
SNM1A-IN-1 (compound 11a) serves as an inhibitor of the DNA damage repair enzyme SNM1A, exhibiting cytotoxic properties [1].
价 格：￥电议型 号：T81140产 地：中国大陆
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T8114Quercetagetin；栎草亭6-Hydroxyquercetin；栎草亭|||6-Hydroxyquercetin
Quercetagetin (6-Hydroxyquercetin) (6-Hydroxyquercetin) is the major flavonoid isolated from Citrus unshiu. It is a moderately potent and selective, cell-permeable pim-1 kinase inhibitor (IC50: 0.34 μM).
价 格：￥电议型 号：T8114产 地：中国大陆
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T81139SNNF(N-Me)GA(N-Me)IL；化合物 SNNF(N-Me)GA(N-Me)ILSNNF(N-Me)GA(N-Me)IL
SNNF(N-Me)GA(N-Me)IL is a biologically active peptide comprising double N-methylated derivatives of a partial IAPP sequence known to be amyloidogenic and cytotoxic.
价 格：￥电议型 号：T81139产 地：中国大陆
