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T17486Azido-PEG12-NHS ester
Azido-PEG12-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T17486产 地:中国大陆
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T17484Azido-PEG12-acid
Azido-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T17484产 地:中国大陆
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T17465Azide-PEG12-Tos叠氮-十二聚乙二醇-对甲苯磺酰酯
Azide-PEG12-Tos is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T17465产 地:中国大陆
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T17464Azide-PEG12-alcohol
Azide-PEG12-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格:¥电议型 号:T17464产 地:中国大陆
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T17408Amino-PEG12-Boc
Amino-PEG12-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T17408产 地:中国大陆
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T17407Amino-PEG12-amineH2N-PEG12-CH2CH2NH2;PEODA13;氨基十三聚乙二醇氨基
Amino-PEG12-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格:¥电议型 号:T17407产 地:中国大陆
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T17406Amino-PEG12-alcohol
Amino-PEG12-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格:¥电议型 号:T17406产 地:中国大陆
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T17405Amino-PEG12-acid
Amino-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T17405产 地:中国大陆
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T14137AG 1295
AG 1295 is a selective platelet-derived growth factor receptor (PDGFR) tyrosine-kinase inhibitor. AG1295 abolishes autophosphorylation of the PDGFR. But it can not affects the autophosphorylation of the EGF receptor[1][2][3][4].
价 格:¥电议型 号:T14137产 地:中国大陆
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T11411GLPG1205GLPG1205
GLPG1205 is potent, selective and orally active GPR84 (a G-protein-coupled receptor) antagonist with a favorable PK/PD profile.?GLPG1205 has anti-inflammatory activity and is used for the treatment of pulmonary fibrosis.?
价 格:¥电议型 号:T11411产 地:美洲
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T11735K-Ras G12C-IN-1K-Ras G12C-IN-1
K-Ras G12C-IN-1 is a novel and irreversible inhibitor of mutant K-ras G12C.
价 格:¥电议型 号:T11735产 地:美洲
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T11736K-Ras G12C-IN-2K-Ras G12C-IN-2
K-Ras G12C-IN-2 is a covalent kras g12c inhibitor.
价 格:¥电议型 号:T11736产 地:美洲
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T11737K-Ras G12C-IN-3K-Ras G12C-IN-3
K-ras G12C inhibitor For more information, please see the following patent. Heterocyclic compounds as covalent inhibitors of G12C mutant K-Ras protein useful for treating cancers.K-Ras G12C-IN-3 is a novel and irreversible inhibitor of mutant K-ras G12C.
价 格:¥电议型 号:T11737产 地:美洲
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T79808KRAS G12C inhibitor 61;化合物 KRAS G12C inhibitor 61KRAS G12C inhibitor 61
KRAS G12C inhibitor 61 (Example 3) demonstrates potent activity by inhibiting phospho-ERK 1/2 in MIA PaCa-2 cells, reflected in an IC50 value of 9 nM. This inhibitor is applicable in the research of pancreatic, colorectal, and lung cancers [1].
价 格:¥电议型 号:T79808产 地:中国大陆
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T79166KRAS G12C inhibitor 60;化合物 KRAS G12C inhibitor 60KRAS G12C inhibitor 60
KRAS G12C Inhibitor 60 (compound 23), a selective inhibitor targeting the Kras-G12C mutation, is utilized in the investigation of lung, colorectal, and pancreatic cancers [1].
价 格:¥电议型 号:T79166产 地:中国大陆
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T79150KRAS G12C inhibitor 59;化合物 KRAS G12C inhibitor 59KRAS G12C inhibitor 59
KRAS G12C Inhibitor 59 is a compound with anticancer properties.
价 格:¥电议型 号:T79150产 地:中国大陆
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T79148PROTAC KRAS G12C degrader-3;化合物 PROTAC KRAS G12C degrader-3PROTAC KRAS G12C degrader-3
PROTAC KRAS G12C Degrader-3 (Comp 283) serves as a potent degrader of KRAS G12C, utilized in cancer research [1].
价 格:¥电议型 号:T79148产 地:中国大陆
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T79072KRAS G12D modulator-1;化合物 KRAS G12D modulator-1KRAS G12D modulator-1
KRAS G12D modulator-1 (compound 6), a potent modulator of KRAS G12D, exhibits IC50 values ranging from 1-10 μM against NEA-G12D, PPI-G12D, and p ERK-AGS, and is utilized in cancer research [1].
价 格:¥电议型 号:T79072产 地:中国大陆
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T79057KRAS G12C inhibitor 58;化合物 KRAS G12C inhibitor 58KRAS G12C inhibitor 58
KRAS G12C inhibitor 58 is utilized in cancer research as an inhibitor of the KRAS G12C mutation [1].
价 格:¥电议型 号:T79057产 地:中国大陆
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T78651Glecirasib;化合物 GlecirasibJAB-21822|||KRAS G12C inhibitor 36;JAB-21822|||KRAS G12C inhibitor 36
Glecirasib (KRAS G12C inhibitor 36) is a potent inhibitor targeting the oncogenic KRAS G12C mutation, a key signaling molecule within the Ras protein family that is crucial for cell growth and development. This compound shows promise for the investigation of cancers mediated by KRAS G12C mutations[1].
价 格:¥电议型 号:T78651产 地:中国大陆