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T9389Thalidomide-PEG4-PropargylE3 Ligase Ligand-Linker Conjugates,Thalidomide-PEG-4-Propargyl,inhibit,Inh
Thalidomide-PEG4-Propargyl is a synthetic E3 ligase ligand-linker conjugate containing a Thalidomide-based cereblon ligand and a linker which can be used in PROTAC technology[1].
价 格:¥电议型 号:T9389产 地:中国大陆
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T6120Pralatrexate10-炔丙基-10-去氮杂氨基蝶呤;普拉曲沙;10-Propargyl-10-deazaaminopterin;Folotyn
Pralatrexate is a folate analogue inhibitor of dihydrofolate reductase (DHFR) exhibiting high affinity for reduced folate carrier-1 (RFC-1) with antineoplastic and immunosuppressive activities.
价 格:¥电议型 号:T6120产 地:中国大陆
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T38173Propargylcholine (bromide)
价 格:¥电议型 号:T38173产 地:中国大陆
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T20129L-PropargylglycineL-炔丙基甘氨酸;(S)-Propargylglycine;(S)-alpha.Propargylglycine;Propargylglycine
L-Propargylglycine is an inhibitor of the enzyme.
价 格:¥电议型 号:T20129产 地:中国大陆
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T19455N-ε-propargyloxycarbonyl-L-lysine hydrochlorideH-?L-?Lys(Poc)?-?OH (hydrochloride);N6-((Prop-2-yn-1-
N-ε-propargyloxycarbonyl-L-lysine hydrochloride is a modified amino acid for cancer therapy development.
价 格:¥电议型 号:T19455产 地:中国大陆
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T18831Thalidomide-propargyl
Thalidomide-propargyl is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Thalidomide-propargyl can be connected to the ligand for protein by a linker to form the IMiD containing PROTACs[1].
价 格:¥电议型 号:T18831产 地:中国大陆
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T18588Propargyl-PEG5-MsPropargyl-PEG6-Ms
Propargyl-PEG5-Ms is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T18588产 地:中国大陆
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T18574Propargyl-PEG17-methaneMPEG16-Propyne
Propargyl-PEG17-methane is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T18574产 地:中国大陆
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T18568Propargyl-PEG11-methane
Propargyl-PEG11-methane is a PEG-based PROTAC linker that can be used to synthesize PROTACs[1].
价 格:¥电议型 号:T18568产 地:中国大陆
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T18566Propargyl-PEG12-bromide
Propargyl-PEG12-bromide is a PEG-based PROTAC linker used to synthesize PROTACs.
价 格:¥电议型 号:T18566产 地:中国大陆
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T18560Propargyl-C1-NHS ester4-戊炔酸琥珀亚胺酯;4-Pentynoic Acid Succinimidyl Ester
Propargyl-C1-NHS ester is a nonclaevable linker for antibody-drug-conjugation (ADC).
价 格:¥电议型 号:T18560产 地:中国大陆
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T16605Propargyl-PEG3-acid丙炔基-二聚乙二醇-羧酸
Propargyl-PEG3-acid is a non-cleavable (3 unit PEG) ADC linker and also a PEG-based PROTAC linker that can be used to synthesis 6-OHDA-PEG3-yne. 6-OHDA-PEG3-yne contains 6-OHDA and Propargyl-PEG3-acid[1].
价 格:¥电议型 号:T16605产 地:中国大陆
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T05804-Pentynoic acidPropargylacetic acid;戊炔酸
4-Pentynoic acid has been used in reactions with 1-bromo-1-alkynes in the presence of a Pd catalyst yields biologically active ynenol lactones. It also is used in a synthesis of a cytotoxic macrolide by ring-closing metathesis of a bis acetylene.
价 格:¥电议型 号:T0580产 地:中国大陆
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T05804-Pentynoic acid4-Pentynoic acid,Propargylacetic acid,
4-Pentynoic acid has been used in reactions with 1-bromo-1-alkynes in the presence of a Pd catalyst yields biologically active ynenol lactones. It also is used in a synthesis of a cytotoxic macrolide by ring-closing metathesis of a bis acetylene.
价 格:¥电议型 号:T0580产 地:美洲
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T12284O-Propargyl-PuromycinO-Propargyl-Puromycin,O-Propargylpuromycin,
O-Propargyl-Puromycin is a potent inhibitor of protein synthesis.
价 格:¥电议型 号:T12284产 地:美洲
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T13876(S,R,S)-AHPC-propargyl(S,R,S)-AHPC-propargyl,VH032-propargyl,VHL ligand 7
(S,R,S)-AHPC-propargyl is a VHL ligand which is used in “click reaction” for PROTACs.
价 格:¥电议型 号:T13876产 地:美洲
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T6120PralatrexatePralatrexate,Folotyn,10-Propargyl-10-deazaaminopterin
Pralatrexate is a folate analogue inhibitor of dihydrofolate reductase (DHFR) exhibiting high affinity for reduced folate carrier-1 (RFC-1) with antineoplastic and immunosuppressive activities.
价 格:¥电议型 号:T6120产 地:美洲
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T837996-alkyne NAD+ sodium;化合物 6-alkyne NAD+ sodiumβ-Nicotinamide-N6-propargyladenine dinucleotide|||6-Par
6-alkyne NAD+, a clickable variant of the signaling molecule and enzyme cofactor NAD+, facilitates the fluorescent tagging for the detection of poly(ADP-ribose) polymerase (PARP) protein substrates.
价 格:¥电议型 号:T83799产 地:中国大陆
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T77891Propargyl-PEG4-GGFG-DXd;化合物 Propargyl-PEG4-GGFG-DXdPropargyl-PEG4-GGFG-DXd
Propargyl-PEG4-GGFG-DXd is a drug-linker conjugate for antibody-drug conjugates (ADCs), comprising an ADC linker and the DNA topoisomerase I inhibitor known as DXd [1].
价 格:¥电议型 号:T77891产 地:中国大陆
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T750397,8-Dihydro-8-oxo-7-propargyl guanosine;化合物 7,8-Dihydro-8-oxo-7-propargyl guanosine7,8-Dihydro-8-oxo
7,8-Dihydro-8-oxo-7-propargyl guanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis , etc [1] .
价 格:¥电议型 号:T75039产 地:中国大陆