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T81378PROTAC IRAK4 ligand-3;化合物 PROTAC IRAK4 ligand-3PROTAC IRAK4 ligand-3
PROTAC IRAK4 Ligand-3 serves as a ligand for PROTAC IRAK4 Degrader-7 and is utilized in cancer research [1].
价 格:¥电议型 号:T81378产 地:中国大陆
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T80928TSPO ligand-3;化合物 TSPO ligand-3TSPO ligand-3
TSPO ligand-3, functioning as an AUTAC2 ligand, incorporates both a p-fluorobenzylguanine (FBnG) and a synthetic ligand of FKBP (SLF) moiety, leading to the substantial inhibition of FKBP12 in HeLa cells [1].
价 格:¥电议型 号:T80928产 地:中国大陆
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T80584Anti-Mouse Fas Ligand Antibody (MFL3);化合物 Anti-Mouse Fas Ligand Antibody (MFL3)Anti-Mouse Fas Ligand
Anti-Mouse Fas Ligand Antibody is an Armenian hamster-derived IgG inhibitor that targets the mouse Fas Ligand.
价 格:¥电议型 号:T80584产 地:中国大陆
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T80512Thrombin receptor peptide ligand;化合物 Thrombin receptor peptide ligandThrombin receptor peptide ligan
Thrombin receptor peptide ligand, a thrombin receptor antagonist, serves as an antithrombotic agent [1].
价 格:¥电议型 号:T80512产 地:中国大陆
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T79577CB2 PET Radioligand 1;化合物 CB2 PET Radioligand 1CB2 PET Radioligand 1
CB2 PET Radioligand 1 (compound [18F]9) is a positron emission tomography (PET) radioligand with high affinity for the human cannabinoid receptor 2 (hCB2, Ki=7.7 nM). It is synthesized via Cu-mediated 18F-fluorination and demonstrates significant brain uptake in a mouse model of neuroinflammation [1].
价 格:¥电议型 号:T79577产 地:中国大陆
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T79184FKBP51F67V-selective antagonist Ligand2;化合物 FKBP51F67V-selective antagonist Ligand2FKBP51F67V-select
FKBP51F67V-selective antagonist Ligand2 (example 3-3), a potent ligand, selectively binds to the FKBP51 F67V variant, with no affinity for wild-type FKBP51 or FKBP52 [1]. It effectively reverses the anxiogenic phenotype resulting from FKBP51 F67V overexpression in the amygdala.
价 格:¥电议型 号:T79184产 地:中国大陆
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T79003HDAC ligand-1;化合物 HDAC ligand-1HDAC ligand-1
HDAC ligand-1 is a synthetic precursor utilized in the production of PROTAC-based HDAC degraders [1].
价 格:¥电议型 号:T79003产 地:中国大陆
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T78736D3R ligand 1;化合物 D3R ligand 1D3R ligand 1
D3R Ligand 1 (compound 23b) is a potent, selective antagonist of the dopamine D3 receptor (Ki=66 nM), incorporating a THPB template. It inhibits both G-protein- and β-arrestin-mediated signaling pathways [1].
价 格:¥电议型 号:T78736产 地:中国大陆
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T77928PROTAC PTK6 ligand-1;化合物 PROTAC PTK6 ligand-1PROTAC PTK6 ligand-1
PROTAC PTK6 ligand-1 serves as an intermediate in the synthesis of BTK kinase inhibitors [1] and is utilized in the preparation of ARD-61 [2].
价 格:¥电议型 号:T77928产 地:中国大陆
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T77921PROTAC BRD4 ligand-2 hydrochloride;化合物 PROTAC BRD4 ligand-2 hydrochloridePROTAC BRD4 ligand-2 hydroc
PROTAC BRD4 Ligand-2 Hydrochloride serves as a ligand targeting the BRD4 protein, specifically designed for use with PROTAC CFT-2718.
价 格:¥电议型 号:T77921产 地:中国大陆
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T7763Thalidomide-4-OH化合物Thalidomide-4-OHCereblon ligand 2|||E3 ligase Ligand 2
Thalidomide-4-OH (E3 ligase Ligand 2) (Cereblon ligand 2) is the Thalidomide-based Cereblon ligand used to recruit of CRBN protein. Thalidomide-4-OH (Cereblon ligand 2) is a linker to form PROTACs
价 格:¥电议型 号:T7763产 地:中国大陆
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T7760Thalidomide-O-amido-C3-NH2 TFA;化合物Thalidomide-O-amido-C3-NH2 TFACereblon Ligand-Linker Conjugates 16
Thalidomide-O-amido-C3-NH2 TFA (Cereblon Ligand-Linker Conjugates 16 TFA) is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-O-amido-C3-NH2 TFA incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
价 格:¥电议型 号:T7760产 地:中国大陆
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T7759Thalidomide-O-amido-C4-NH2 TFA;化合物T7759E3 ligase Ligand-Linker Conjugates 19 TFA|||Cereblon Ligand-L
Thalidomide-O-amido-C4-NH2 TFA (E3 ligase Ligand-Linker Conjugates 19 TFA) is a synthesized E3 ligase ligand-linker conjugate.
价 格:¥电议型 号:T7759产 地:中国大陆
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T7758Thalidomide-O-amido-PEG3-C2-NH2 TFA;化合物T7758E3 ligase Ligand-Linker Conjugates 14 TFA|||Cereblon Lig
Thalidomide-O-amido-PEG3-C2-NH2 TFA (Cereblon Ligand-Linker Conjugates 3 (TFA)) is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-O-amido-PEG3-C2-NH2 TFA incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
价 格:¥电议型 号:T7758产 地:中国大陆
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T7757Cereblon Ligand -Linker Conjugates 2 TFA化合物 T7757Cereblon Ligand -Linker Conjugates 2 TFA|||Cereblon
Cereblon Ligand -Linker Conjugates 2 TFA is an E3 ligase ligand-linker conjugate incorporating the Thalidomide-based cereblon ligand and a linker.
价 格:¥电议型 号:T7757产 地:中国大陆
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T7755Thalidomide 4-fluoride2-(2,6-二氧代-哌啶-3-基)-4-氟基-异吲哚-1,3-二酮E3 ligase Ligand 4|||2-(2,6-二氧代-哌啶-3-基)-4-氟基
Thalidomide 4-fluoride (E3 ligase Ligand 4) (Cereblon ligand 4) is the Thalidomide-based Cereblon ligand. Thalidomide 4-fluoride can be used in the recruitment of CRBN protein. Thalidomide 4-fluoride (Cereblon ligand 4) can be connected to the ligand for IRAK4 protein by a linker to form PROTAC IRAK4 degrader-1.
价 格:¥电议型 号:T7755产 地:中国大陆
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T7753Thalidomide-O-COOH;化合物Thalidomide-O-COOHinhibit|||Ligands for E3 Ligase|||TCE35031|||ThalidomideOCOO
Thalidomide-O-COOH (Cereblon ligand 3) is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a linker to form PROTACs.
价 格:¥电议型 号:T7753产 地:中国大陆
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T7752(S,R,S)-AHPC-Me;化合物(S,R,S)-AHPC-MeVHL ligand 2|||E3 ligase Ligand 1A;VHL ligand 2|||E3 ligase Ligand
(S,R,S)-AHPC-Me (E3 ligase Ligand 1A) (VHL ligand 2) is the (S,R,S)-AHPC-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein[1]. (S,R,S)-AHPC-Me can be used to synthesize ARV-771. ARV-771 is a von Hippel-Landau (VHL) E3 ligase-based BET PROTAC degrader. ARV-771 potently degrades BET protein in castration-resistant prostate cancer (CRPC) cells with a DC50 <1 nM.
价 格:¥电议型 号:T7752产 地:中国大陆
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T76568Aminopeptidase N Ligand (CD13) NGR peptide;化合物 Aminopeptidase N Ligand (CD13) NGR peptideAminopeptid
Aminopeptidase N Ligand (CD13) NGR peptide, a polypeptide that targets CD13, functions as a carrier for mediating intracellular transmission and is commonly utilized in cancer research [1] [2].
价 格:¥电议型 号:T76568产 地:中国大陆
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T74654Neuropeptide Y5 receptor ligand-1;化合物 Neuropeptide Y5 receptor ligand-1Neuropeptide Y5 receptor liga
Neuropeptide Y5 receptor ligand-1 (Compound 54), a carbazole derivative, acts as a powerful antagonist to the neuropeptide Y5 (NPY-5) receptor [1].
价 格:¥电议型 号:T74654产 地:中国大陆