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T19590Trehalose 6-behenate；海藻糖 6-山嵛酸酯Trehalose 6-behenate
Trehalose 6-behenate is a Th1/Th17 skewing vaccine adjuvant.
价 格：￥电议型 号：T19590产 地：中国大陆
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T1951Asenapine Maleate；阿塞那平马来酸盐Org 5222 maleate|||Org 5222；Org 5222 maleate|||Org 5222|||马来酸阿塞那平|||阿塞那平马来
Asenapine Maleate (Org 5222 maleate) is a second generation (atypical) antipsychotic agent that is taken sublingually and used in the treatment of schizophrenia and manic or mixed episodes associated with bipolar 1 disorder. Asenapine is associated with a low rate of transient and mild serum aminotransferase elevations during therapy but has not been linked to instances of clinically apparent acute liver injury.
价 格：￥电议型 号：T1951产 地：中国大陆
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T19236Cholesteryl behenate；胆固醇山萮酸酯Cholesteryl docosanoate|||Cholesterol behenate；Cholesteryl docosanoate||
Cholesteryl behenate is a standard in electrospray ionization tandem mass spectrometry for the analysis of cholesteryl esters and cholesterol.
价 格：￥电议型 号：T19236产 地：中国大陆
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T191434-(6-Bromo-2-benzothiazolyl)benzenamine；化合物 T191434-(6-Bromo-2-benzothiazolyl)benzenamine
4-(6-Bromo-2-benzothiazolyl)benzenamine is a β-amyloid PET tracer and can be used in the diagnosis of neurological diseases.
价 格：￥电议型 号：T19143产 地：中国大陆
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T191424-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine；化合物 T191424-(6-Bromo-2-benzothiazolyl)-N-methylbenz
4-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine is a potent amyloid imaging agent that binds to Amyloid-β (1-40) (KD: 1.7 nM).
价 格：￥电议型 号：T19142产 地：中国大陆
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T19112LSacubitril Enantiomer；LCZ 696杂质A2R,4S-Sacubitril|||ahu377 isomer 2；2R,4S-Sacubitril|||LCZ 696杂质A|||a
Sacubitril Enantiomer (ahu377 isomer 2) is the enantiomer of Sacubitril which is a neprilysin inhibitor.
价 格：￥电议型 号：T19112L产 地：中国大陆
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T191122R,4S-Sacubitril；LCZ 696杂质ASacubitril Enantiomer|||ahu377 isomer 2；LCZ 696杂质A|||Sacubitril Enantiome
2R,4S-Sacubitril (Sacubitril Enantiomer) is the impurity of Sacubitril which is a neprilysin inhibitor.
价 格：￥电议型 号：T19112产 地：中国大陆
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T18919Bathophenanthroline；红菲咯啉Bathophenanthroline
Bathophenanthroline is a compound used for the measurement of iron concentrations in aqueous, urine, and serum samples by colorimetry.
价 格：￥电议型 号：T18919产 地：中国大陆
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T1867Otenaproxesul；化合物ATB 346ATB 346；ATB 346
Otenaproxesul (ATB 346) is a novel hydrogen sulphide-releasing derivative of naproxen with markedly reduced toxicity.
价 格：￥电议型 号：T1867产 地：中国大陆
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T18070Lenalidomide-propargyl-C2-NH2 hydrochloride；化合物 T18070Lenalidomide-propargyl-C2-NH2 hydrochloride
Lenalidomide-propargyl-C2-NH2 hydrochloride is a compound that features a cereblon (CRBN) ligand for the E3 ubiquitin ligase, as well as a linker. It is utilized in the development of the PROTAC MD-224[1] system.
价 格：￥电议型 号：T18070产 地：中国大陆
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T18069Lenalidomide-propargyl-C2-amido-Ph-NH2 hydrochloride；化合物 T18069Lenalidomide-propargyl-C2-amido-Ph-NH
Lenalidomide-propargyl-C2-amido-Ph-NH2 hydrochloride is a chemical compound that features a cereblon (CRBN) ligand, functioning as an E3 ubiquitin ligase, along with a linker. It can be utilized to create the PROTAC MD-224[1].
价 格：￥电议型 号：T18069产 地：中国大陆
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T18068Lenalidomide-PEG3-iodine；化合物 T18068Lenalidomide-PEG3-iodine
Lenalidomide-PEG3-iodine, an E3 ligase ligand-linker conjugate, consists of a cereblon-based Lenalidomide ligand and a 3-unit polyethylene glycol (PEG) linker. This compound is utilized in creating various proteolysis targeting chimeras (PROTACs), including the highly effective PROTAC BTK degrader SJF620, which has a degradation concentration 50 (DC50) of 7.9 nM[1].
价 格：￥电议型 号：T18068产 地：中国大陆
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T18067Lenalidomide-PEG1-azide；化合物 T18067Lenalidomide-PEG1-azide
Lenalidomide-PEG1-azide is an E3 ligase ligand-linker conjugate that incorporates the cereblon ligand based on Lenalidomide and a linker. It is designed for use in the development of PROTAC BRD4 Degrader-2[1].
价 格：￥电议型 号：T18067产 地：中国大陆
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T18066Lenalidomide-OH；化合物Lenalidomide-OHLenalidomide-OH
Lenalidomide-OH is a ligand of cereblon (CRBN), serving as an analog to Lenalidomide for E3 ubiquitin ligase. It is utilized in the recruitment of CRBN protein. Additionally, Lenalidomide-OH can be conjugated to a protein ligand through a linker, resulting in the formation of PROTACs. An example of a PROTAC BTK degrader incorporating Lenalidomide-OH is SJF620.
价 格：￥电议型 号：T18066产 地：中国大陆
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T18065Lenalidomide-C9-aldehyde；化合物 T18065Lenalidomide-C9-aldehyde
Lenalidomide-C9-aldehyde is a synthesized E3 ligase ligand-linker conjugate that incorporates the Lenalidomide based cereblon ligand and a linker. Lenalidomide-C9-aldehyde can be used in the synthesis of a series of PROTACs, such as INY-03-041. INY-03-041 is a potent, highly selective and PROTAC-based pan-Akt degrader. INY-03-041 inhibits Akt1, Akt2 and Akt3 with IC50s of 2.0 nM, 6.8 nM and 3.5 nM, respectively[1].
价 格：￥电议型 号：T18065产 地：中国大陆
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T18064Lenalidomide-Br；3-(4-溴-1-氧代异吲哚啉-2-基)哌啶-2,6-二酮Lenalidomide-Br
Lenalidomide-Br (Compound 41) is a derivative of Lenalidomide, which serves as a ligand for cereblon (CRBN) - an E3 ubiquitin ligase involved in protein recruitment. This compound, Lenalidomide-Br, can be conjugated to a protein ligand through a linker to create PROTACs. For instance, Lenalidomide-Br is utilized as a component in the PROTAC STAT3 degrader SD-36.
价 格：￥电议型 号：T18064产 地：中国大陆
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T18063Lenalidomide-acetylene-C5-COOH；化合物 T18063Cereblon ligand-linker Conjugate；Cereblon ligand-linker Con
Lenalidomide-acetylene-C5-COOH (compound 43; Cereblon ligand-linker Conjugate) serves as a Lenalidomide-based Cereblon ligand that facilitates the recruitment of the CRBN protein. This compound can be connected to the protein´s ligand through a linker, resulting in the formation of PROTAC[1].
价 格：￥电议型 号：T18063产 地：中国大陆
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T1796Otenabant hydrochloride；奥替那班Otenabant (CP-945598) HCl|||CP 945598 Hydrochloride|||Otenabant；奥替那班|||O
Otenabant hydrochloride (Otenabant) (CP-945598) is a competitive, high affinity, selective antagonist of the CB1 receptor (Ki: 0.7 nM).
价 格：￥电议型 号：T1796产 地：中国大陆
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T17928Lenalidomide-C5-NH2；化合物 T17928E3 ligase Ligand-Linker Conjugates 31|||Cereblon Ligand-Linker Conjuga
Lenalidomide-C5-NH2 is the Lenalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Lenalidomide-C5-NH2 can be connected to the ligand for protein by a linker to form PROTACs[1].
价 格：￥电议型 号：T17928产 地：中国大陆
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T17878Lenalidomide-C4-NH2 hydrochloride；化合物 T17878Cereblon ligand 1 hydrochloride|||E3 ligase Ligand-Linke
Lenalidomide-C4-NH2 hydrochloride is a Cereblon ligand derived from Lenalidomide. It serves as a recruiting agent for the CRBN protein. The compound, known as PROTAC (Compound 24), can be formed by linking Lenalidomide-C4-NH2 hydrochloride to the ligand for the protein. It exhibits inhibitory effects with IC50s of 0.98 nM and 13.7 nM against the growth of RS4;11 and MOLM-13 acute leukemia cell lines, respectively[1].
价 格：￥电议型 号：T17878产 地：中国大陆
