当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3293425
自主品牌
已选条件
-
T9820GPI-1485neurofunctional,regeneration,Inhibitor,ligand,stroke,GPI-1485,GPI 1485,inhibit,immunophilin,
GPI-1485 (GM1485) is a nonimmunosuppressive immunophilin ligand, promoting neurofunctional improvement and neural regeneration following stroke.
价 格：￥电议型 号：T9820产 地：中国大陆
-
T17875Pomalidomide-C2-NH2Inhibitor,E3 Ligase Ligand-Linker Conjugates,PomalidomideC2NH2,Pomalidomide-C-2-N
Pomalidomide-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a linker.
价 格：￥电议型 号：T17875产 地：中国大陆
-
T7758Thalidomide-O-amido-PEG3-C2-NH2 TFAE3 Ligase Ligand-Linker Conjugates,Cereblon Ligand-Linker Conjuga
Thalidomide-O-amido-PEG3-C2-NH2 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
-
T17881(S,R,S)-AHPC-C10-NH2PROTAC,(S,R,S) AHPC C10 NH2,Inhibitor,(S,R,S)AHPCC10NH2,E3 Ligase Ligand-Linker
(S,R,S)-AHPC-C10-NH2 is a synthesized E3 ligase ligand-linker conjugate incorporating the (S,R,S)-AHPC based VHL ligand and a linker used for BET-Targeted PROTAC.
价 格：￥电议型 号：T17881产 地：中国大陆
-
T9402Thalidomide-O-C4-NH2 hydrochlorideThalidomide O C4 NH2 hydrochloride,E3 Ligase Ligand-Linker Conjuga
Thalidomide-linker 9 is a synthesized?E3 ligase ligand-linker conjugate?that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
价 格：￥电议型 号：T9402产 地：中国大陆
-
T7833TLX agonist 1TLX agonist-1,transcriptional,TLX agonist 1,repressive,Inhibitor,ligand,inhibit,TLX ago
TLX agonist 1 is an orphan nuclear receptor tailless (TLX, NR2E1) modulator
价 格：￥电议型 号：T7833产 地：中国大陆
-
T13890SMARCA-BD ligand 1 for Protac dihydrochlorideSMARCABD ligand 1 for Protac dihydrochloride,SMARCA BD
SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunits SMARCA2, and used for degrading SMARCA2, based on PROTAC.
价 格：￥电议型 号：T13890产 地：中国大陆
-
T8824CRBN modulator-1CRBN modulator1,CRBN modulator-1,inhibit,CRBN modulator 1,Ligands for E3 Ligase,E3 l
WUN29654 is a Thalidomide analog and CRBN modulator,has an IC50 of 3.5 μM and a Ki of 0.98 μM.
价 格：￥电议型 号：T8824产 地：中国大陆
-
T9382Thalidomide-NH-C2-PEG3-OHinhibit,Inhibitor,Thalidomide-NH-C-2-PEG3-OH,E3 Ligase Ligand-Linker Conjug
Thalidomide-NH-C2-PEG3-OH is an E3 ligase ligand-linker conjugate.
价 格：￥电议型 号：T9382产 地：中国大陆
-
T7752(S,R,S)-AHPC-MeVHL ligand-2,VHL ligand2,Inhibitor,inhibit,Ligands for E3 Ligase,(S,R,S) AHPC Me,(S,R
(S,R,S)-AHPC-Me (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
-
T7904SR 19881SR-19881,estrogen-related receptor,nuclear receptor,amide,SR19881,phenol,ligand binding doma
SR 19881 is a full agonist of ERRγ(EC50 value of 0.39 μM in a binding assay and an EC50 value of 4.7 μM in a cell-based assay).
价 格：￥电议型 号：T7904产 地：中国大陆
-
T13510Sigma-LIGAND-1SigmaLIGAND1,Sigma LIGAND 1
Sigma-LIGAND-1 is a selective Sigma Receptor ligand with an IC50s of 16 nM, 19 nM at the DTG site and the PPP site, respectively. Sigma-LIGAND-1 has a Ki of 4000 nM at the dopamine D2 receptor.
价 格：￥电议型 号：T13510产 地：中国大陆
-
T7760Thalidomide-O-amido-C3-NH2 TFAInhibitor,E3 Ligase Ligand-Linker Conjugates 52,E3 Ligase Ligand-Linke
Thalidomide-O-amido-C3-NH2 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
-
T9291Thalidomide-5-OHLigands for E3 Ligase,PROTAC,Inhibitor,Thalidomide5OH,inhibit,CRBN,E3 ligase-recruit
Thalidomide-5-OH is the Thalidomide-based cereblon ligand that used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a linker to form PROTAC.
价 格：￥电议型 号：T9291产 地：中国大陆
-
T9809E3 ligase Ligand 23inhibit,Inhibitor,Cereblon,Aiolos,ubiquitin proteasome,Ligands for E3 Ligase,Ikar
E3 ligase Ligand 23 is a cereblon binder and degrades Ikaros or Aiolos through ubiquitin proteasome.
价 格：￥电议型 号：T9809产 地：中国大陆
-
TP1484Lα2β1 Integrin Ligand Peptide acetateα2β1 Integrin Ligand Peptide acetate
α2β1 Integrin Ligand Peptide acetate is a potential antagonist of α2β1 integrin receptor. α2β1 Integrin Ligand Peptide interacts with the α2β1 integrin receptor on the cell membrane and mediates extracellular signals into cells.
价 格：￥电议型 号：TP1484L产 地：中国大陆
-
T9061EN4EN4,ligand,Myc,tumorigenesis,transcriptional,inhibit,Inhibitor,EN 4,covalent,C171,c-Myc,EN-4
EN4 MYC inhibitor is a covalent ligand that targets cysteine 171 (C171) of MYC. It is selective for c-MYC over N-MYC and L-MYC, and inhibits MYC transcriptional activity, downregulates MYC targets, and impairs tumorigenesis.
价 格：￥电议型 号：T9061产 地：中国大陆
-
T7753Thalidomide-O-COOHinhibit,Ligands for E3 Ligase,ThalidomideOCOOH,Inhibitor,Thalidomide O COOH,Cerebl
Thalidomide-O-COOH 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
-
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
-
T6812LCyclo(-RGDfK) TFAligand,αvβ3 integrin,Cyclo( RGDfK) TFA,inhibit,Integrin,Microvasculature,cancer,Cyc
Cyclo(-RGDfK) is a selective αvβ3 integrin inhibitor(IC50 : 0.94 nM).
价 格：￥电议型 号：T6812L产 地：中国大陆
