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
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:3700494
已选条件
-
T7202ITEITE,Aryl Hydrocarbon Receptor,Inhibitor,inhibit,AhR
ITE is a potent endogenous agonist of aryl hydrocarbon receptor (AhR) (Ki : 3 nM), has immunosuppressive activity.
价 格:¥电议型 号:T7202产 地:中国大陆
-
T7549Talnetantschizophrenia,SB223412,NK receptor,Inhibitor,hNK-2,Talnetant,Neurokinin Receptor,Tachykinin
Talnetant is a selective, competitive, brain-penetrant NK3 receptor antagonist with the ability to modulate mesolimbic and mesocortical dopaminergic neurotransmission
价 格:¥电议型 号:T7549产 地:中国大陆
-
T7509PD 117519CI-947,PD-117519,Adenosine Receptor,Inhibitor,P1 receptor,PD117519,PD 117519,inhibit,CI 947
PD 117519 is an agonist of adenosine receptor
价 格:¥电议型 号:T7509产 地:中国大陆
-
T7626Budipinemonoamine oxidase type B (MAO-B),inhibit,CNS disorders,Parkinson disease,Budipine,Inhibitor,
Budipine is a low affinity, N-methyl-D-aspartate receptor antagonist,is an antiparkinsonian agent.
价 格:¥电议型 号:T7626产 地:中国大陆
-
T9140NAcM-OPT HCl(2089293-61-6 free base)NAcMOPT HCl(2089293616 free base),NAcM OPT HCl(2089293 61 6 free
NAcM-OPT HCL is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor that targets N-Acetyl-UBE2M (E2 conjugating enzyme, UBC12) interaction with DCN1 with IC50 of 79 nM.
价 格:¥电议型 号:T9140产 地:中国大陆
-
T6788Bitopertininhibit,Bitopertin,RG 1678,RO-4917838,RG-1678,GlyT,Inhibitor,RO 4917838,Glycine transporte
Bitopertin (RG1678, RO-4917838) is a potent inhibitor of glycine transporter 1 (GlyT1), with Ki of 8.1 nM for human hGlyT1b and IC50 of 22-25 nM in Chinese hamster ovary cells.
价 格:¥电议型 号:T6788产 地:中国大陆
-
T9908PembrolizumabPembrolizumab
Pembrolizumab is a humanized monoclonal antibody inhibiting the PD-1 receptor and the first in the class of agents called the HER2 dimerization inhibitors that impairs the ability of HER2 to bind to other members of the HER family.
价 格:¥电议型 号:T9908产 地:中国大陆
-
TJS1382TaraxeroneAldehyde Dehydrogenase (ALDH),Taraxerone,Inhibitor,alcohol,enhancer,ALDH,inhibit,ADH
Taraxerone has allelopathic and antifungal effects.Taraxerone prevents catalase, superoxide dismutase, and reduces glutathione concentrations from the decrease induced by ethanol administration with the concentration dependent manner.
价 格:¥电议型 号:TJS1382产 地:中国大陆
-
TP1918LLys-[Des-Arg9]Bradykinin,TFALys-[Des-Arg-9]Bradykinin,TFA,Lys [Des Arg9]Bradykinin,TFA,Lys[DesArg9]B
Lys-[Des-Arg9]Bradykinin,TFA is Endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9]-Bradykinin.
价 格:¥电议型 号:TP1918L产 地:中国大陆
-
TN1421Bacopaside IIApoptosis,Bacopaside II,Inhibitor,inhibit
Bacopaside II is a potential anti-angiogenic agent, it can reduce endothelial cell migration and tubulogenesis and induce apoptosis.
价 格:¥电议型 号:TN1421产 地:中国大陆
-
TJS0328Nordalberginpromyelocytic,Inhibitor,coumarin,HL-60,cells,leukemia,differentiation,Nordalbergin,inhib
价 格:¥电议型 号:TJS0328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
-
TN1787Isomucronulatol 7-O-glucosideinhibit,Inhibitor,IL-12p40,Isomucronulatol 7Oglucoside,Isomucronulatol
Isomucronulatol 7-O-beta-glucoside is a natural product
价 格:¥电议型 号:TN1787产 地:中国大陆
-
T9095Necrostatin-34Necrostatin 34,RIP kinase,FADD,Necrostatin-34,RIPK,inhibit,RIPK1,Receptor-interacting
Necrostatin-34 is a RIPK1 kinase inhibitor, stabilizing RIPK1 kinase in an inactive conformation by occupying a distinct binding pocket in the kinase domain.
价 格:¥电议型 号:T9095产 地:中国大陆
-
T86112,3-dihydro-1H-indene-5-sulfonamide2,3 dihydro 1H indene 5 sulfonamide,2,3dihydro1Hindene5sulfonamid
2,3-dihydro-1H-indene-5-sulfonamide is Carbonic anhydrase 12 (human) inhibitor.
价 格:¥电议型 号:T8611产 地:中国大陆
-
T8659K-Ras-PDEδ-IN-1KRasPDEδIN1,PDEδ,cancer,pyrazolopyridazinone-based,inhibit,K Ras PDEδ IN 1,Inhibitor,
K-Ras-PDEδ-IN-1 is a potent inhibitor of competitive K-Ras-PDEδ.It binds to the farnesyl binding pocket of PDEδ(Kd of 8 nM).
价 格:¥电议型 号:T8659产 地:中国大陆
-
T7025Rehmannioside DInhibitor,inhibit,Rehmannioside D
Rehmannioside D is a carotenoid glycoside that existed in the roots of Rehmannia glutinosa.
价 格:¥电议型 号:T7025产 地:中国大陆
-
T8217Enzalutamide carboxylic acidprostate,Enzalutamide carboxylic acid,metastatic,MDV3100 carboxylic acid
Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .
价 格:¥电议型 号:T8217产 地:中国大陆
-
T8557N-terminally acetylated Leu-enkephalinN terminally acetylated Leu enkephalin,Nterminally acetylated
Leu-enkephalin is a five amino acid endogenous peptide that acts as an agonist at opioid receptors.N-terminally acetylated Leu-enkephalin is the N-terminally acetylated form of Leu-enkephalin.
价 格:¥电议型 号:T8557产 地:中国大陆
-
TMO268510-Hydroxydecanoic Acid10Hydroxydecanoic Acid,NSC15139,NSC-15139,10-Hydroxydecanoic acid,inhibit,Inh
It has antibacterial, anti - cancer and anti - radiation activity.
价 格:¥电议型 号:TMO2685产 地:中国大陆