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T14862Caprylic/Capric Triglyceride;辛癸酸甘油酯Caprylic/Capric Triglyceride
Caprylic/Capric Triglyceride, a compound consisting of triglycerides and esters derived from fractionated vegetable oil, and fatty acids from coconut and palm kernel oils, serves as a food additive and is utilized in cosmetics. This substance demonstrates outstanding oxidation stability.
价 格:¥电议型 号:T14862产 地:中国大陆
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T1483Citalopram hydrobromide;氢溴酸西酞普兰Lu 10-171|||Nitalapram HBr|||Bonitrile HBr|||XU-62-320|||Lu 10-171 HB
Citalopram hydrobromide (XU-62-320) , a selective serotonin reuptake inhibitor (SSRI), selectively inhibits the CNS neuronal reuptake of serotonin, thereby potentiating serotonergic activity in the central nervous system (CNS). Citalopram hydrobromide is the orally bioavailable hydrobromide salt of the racemic bicyclic phthalene derivative citalopram with antidepressant activity. This agent has minimal effects on the CNS neuronal reuptake of norepinephrine (NE) and dopamine (DA).
价 格:¥电议型 号:T1483产 地:中国大陆
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T14762Boc-PEG4-sulfonic acid;化合物 T14762Boc-PEG4-sulfonic acid
Boc-PEG4-sulfonic acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14762产 地:中国大陆
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T14682BMS-962212;化合物 T14682BMS-962212
BMS-962212, a direct, reversible, and selective factor XIa (FXIa) inhibitor, demonstrates fast pharmacodynamic (PD) response onset and rapid elimination with a well-tolerated profile. It dependently increases activated partial thromboplastin time and decreases FXI clotting activity exposure [1].
价 格:¥电议型 号:T14682产 地:中国大陆
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T14662Bis-propargyl-PEG9;化合物 T14662Bis-propargyl-PEG9
Bis-propargyl-PEG9 is a PEG-based PROTAC linker employed in the synthesis of PROTACs. It is specifically utilized to synthesize the bivalent ligands of estrogen receptor[1].
价 格:¥电议型 号:T14662产 地:中国大陆
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T14629Bis-PEG10-acid;化合物 T14629Bis-PEG10-acid
Bis-PEG10-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14629产 地:中国大陆
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T14628Bis-PEG1-PFP ester;化合物 T14628Bis-PEG1-PFP ester
Bis-PEG1-PFP ester is a non-cleavable ADC linker incorporating a 1-unit PEG moiety, specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格:¥电议型 号:T14628产 地:中国大陆
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T14627Bis-PEG1-NHS ester;化合物 T14627Bis-PEG1-NHS ester
Bis-PEG1-NHS ester is a non-cleavable 1-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs.
价 格:¥电议型 号:T14627产 地:中国大陆
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T14626Bis-PEG1-acid;化合物 T14626Bis-PEG1-acid
Bis-PEG1-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14626产 地:中国大陆
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T14625Bis-Mal-PEG3;化合物 T14625Bis-Mal-PEG3
Bis-Mal-PEG3 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14625产 地:中国大陆
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T14624Bis-Mal-Lysine-PEG4-TFP ester;化合物 T14624Bis-Mal-Lysine-PEG4-TFP ester
Bis-Mal-Lysine-PEG4-TFP ester, a PEG-based PROTAC linker, facilitates PROTAC synthesis[1].
价 格:¥电议型 号:T14624产 地:中国大陆
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T14623Bis-Mal-Lysine-PEG4-acid;化合物 T14623Bis-Mal-Lysine-PEG4-acid
Bis-Mal-Lysine-PEG4-acid is a PEG-based PROTAC linker utilized for PROTAC synthesis[1].
价 格:¥电议型 号:T14623产 地:中国大陆
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T14622Bis-Biotin-PEG23;化合物 T14622Bis-Biotin-PEG23
Bis-Biotin-PEG23 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14622产 地:中国大陆
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T14621Bis-aminooxy-PEG7;化合物 T14621Bis-aminooxy-PEG7
Bis-aminooxy-PEG7 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14621产 地:中国大陆
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T14620Bis-aminooxy-PEG4;化合物 T14620Bis-aminooxy-PEG4
Bis-aminooxy-PEG4 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T14620产 地:中国大陆
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T1462Captopril;卡托普利SQ 14225|||SQ-14534|||SA333;SQ 14225|||甲巯丙脯酸|||卡托普利|||SQ-14534|||SA333
Captopril (SA333) is a potent and specific inhibitor of peptidyl-dipeptidase A. It blocks the conversion of angiotensin I to angiotensin II, a vasoconstrictor and important regulator of arterial blood pressure.
价 格:¥电议型 号:T1462产 地:中国大陆
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T14569BI8626;化合物 BI8626BI8626
BI8626 is a ubiquitin ligase HUWE1 inhibitor with protective effects against spontaneous desiccation syndrome in NOD/ShiLtj mice.BI8626 inhibits intracellular cholesterol and decreases the expression of phosphorylated ZAP-70, CD25, and other activation markers, and inhibits the proliferation of CD4 T-cells.
价 格:¥电议型 号:T14569产 地:中国大陆
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T14568BI8622;化合物 T14568BI8622
BI8622 is an ubiquitin ligase HUWE1 inhibitor (IC50: 3.1 μM).
价 格:¥电议型 号:T14568产 地:中国大陆
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T14566BI-9627;化合物 T14566BI-9627
BI-9627 is an inhibitor of sodium-hydrogen exchanger isoform 1 (NHE1) (EC50: 31 nM).
价 格:¥电议型 号:T14566产 地:中国大陆
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T14493Balapiravir化合物 T14493R1626|||Ro 4588161
Balapiravir (R1626, Ro 4588161) is the prodrug of a nucleoside analogue inhibitor of the hepatitis C virus (HCV) RNA-dependent RNA polymerase (R1479, RG1479). IC50 Value: Target: HCV Balapiravir was discontinued for safety reasons in 28-36% of patients (most often for lymphopenia) and the percentage of patients with serious adverse events (especially hematological, infection, ocular events) was dose related. Balapiravir (R1626) is the tri-isobutyrate ester prodrug of R1479 under clinical develop
价 格:¥电议型 号:T14493产 地:中国大陆