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产品数:86101
参观次数:3519811
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T7013VorapaxarProtease Activated Receptor (PAR),Inhibitor,SCH-530348,Vorapaxar,SCH530348,Thrombin recepto
Vorapaxar (SCH 530348) is an effective and orally active thrombin receptor (PAR-1) antagonist (Ki: 8.1 nM).
价 格:¥电议型 号:T7013产 地:中国大陆
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TN1153Polyporenic acid Ccell,Apoptosis,inhibit,Inhibitor,lung,cancer,NSCLC,Polyporenic acid C
Polyporenic acid C shows inhibitory activity against human collagenase.
价 格:¥电议型 号:TN1153产 地:中国大陆
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T8985NSC45586pleckstrin homology domain and leucine-rich repeat protein phosphatase,NSC-45586,NSC45586,in
NSC45586 is a protein phosphatase PHLPP inhibitor, which is selective for PHLPP1 and PHLPP2.
价 格:¥电议型 号:T8985产 地:中国大陆
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T8760NNMTiNNMTi,inhibit,fusion,muSC,muscle stem cell,NNMT,Inhibitor,regenerative
NNMTi is a substrate site-targeting, selective nicotinamide N-methyltransferase (NNMT) inhibitor (IC50 = 1.2 μM; 50 μM SAM, 100 μM NCA) that reduces 3T3-L1 lipogenesis (EC50 = 30μM) and adipocytes 1-methylnicotinamide level (EC50 = 2.3 μM) without affecting related methyltransferases & enzymes in the NAD+ salvage pathway
价 格:¥电议型 号:T8760产 地:中国大陆
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T60554Schnurri-3 inhibitor-1
Schnurri-3 inhibitor-1 is a potent inhibitor of schnurri-3, an essential regulator of adult bone formation. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in Shn3FFL (osteoblast cell line, AC50= 2.09 μM). Schnurri-3 inhibitor-1 has research value in osteoporosis.
价 格:¥电议型 号:T60554产 地:中国大陆
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T7946AER-271Inhibitor,AER-271,AQP4,AER-270,stroke,inhibit,aquaporin-4,injury,AER 271,acute,AER271,CNS,isc
AER-271 is an inhibitor of aquaporin-4.
价 格:¥电议型 号:T7946产 地:中国大陆
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T60148MSC-4106MSC4106
MSC-4106 is an orally active and potent inhibitor of YAP/TAZ-TEAD. MSC-4106 inhibits TEAD1 or TEAD3 auto-palmitoylation and exhibits inhibitory effect on NCI-H226 tumor xenograft model [1].
价 格:¥电议型 号:T60148产 地:中国大陆
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T20692LSchistoflrfamide acetateSchistoflrfamide acetate
Schistoflrfamide acetate is isolated from the grasshopper, Schistocerca gregaria. Schistoflrfamide acetate elicited an immediate effect on the basal membrane potential of the opalescent tubule gland cells in insects.
价 格:¥电议型 号:T20692L产 地:中国大陆
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T81722-O-α-D-Glucopyranosyl-L-ascorbic AcidInhibitor,2 O α D Glucopyranosyl L ascorbic Acid,inhibit,2OαDG
ASCORBYL GLUCOSIDE is a glucoside derivative of ascorbic acid, shows anti-cancer activity after enzymatic hydrolysis to ascorbic acid
价 格:¥电议型 号:T8172产 地:中国大陆
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T9019JHU37152JHU37152,inhibit,hM3Dq,Clozapine,Inhibitor,DREADD,Muscarinic acetylcholine receptor,mAChR,hM
JHU 37152 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.8 nM and 8.7 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 5 nM and 0.5 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格:¥电议型 号:T9019产 地:中国大陆
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T7837SR8278Duchenne muscular dystrophy,inhibit,metabolism,biological rhythm,Alzheimer’s disease,SR-8278,S
SR8278 is an REV-ERBα antagonist(EC50 = 0.47 μM), blocking activation of the receptor by the synthetic agonist GSK 4112
价 格:¥电议型 号:T7837产 地:中国大陆
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T9230KM 91104V-ATPase human HSC,a3-b2 subunits,KM-91104,KM 91104,Inhibitor,KM91104,Proton Pump,cell-perme
KM 91104 is a cell permeable inhibitor of V-ATPase. KM91104 specifically targets the interaction between V-ATPase subunit A3 and subunit B2.
价 格:¥电议型 号:T9230产 地:中国大陆
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T9085JFD01307SCJFD-01307SC,Inhibitor,Bacterial,JFD01307SC,inhibit
JFD01307SC is a glutamine synthetase inhibitor. It is anti-tuberculosis agent and acts as a mimic of L-Glutamate and thus target enzymes involved in glutamine biosynthesis.
价 格:¥电议型 号:T9085产 地:中国大陆
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T7426ALSTERPAULLONECDK5,GSK-3,p35,NSC-705701,9-Nitropaullone,NSC705701,ALSTERPAULLONE,Glycogen synthase k
Alsterpaullone is a Cyclin-Dependent Kinase Inhibitor, Mediated Toxicity in HeLa Cells Through Apoptosis-Inducing Effec
价 格:¥电议型 号:T7426产 地:中国大陆
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T6S1918Schisantherin Binhibit,Schisantherin B,Abeta,β-amyloid peptide,Schisantherin-B,Amyloid-β,Inhibitor
1. Schisantherin B shows good effect in lowering the serum glutamic-pyruvic transaminase level of the patients suffering from chronic virus hepatitis.
价 格:¥电议型 号:T6S1918产 地:中国大陆
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T6561Laquinimodinhibit,multiple sclerosis,relapsing remitting,carboxamide,Nuclear factor-kappaB,Apoptosis
Laquinimod is an effective immunomodulator, which is currently under development in phase III trials for the treatment of multiple sclerosis as an oral therapy.
价 格:¥电议型 号:T6561产 地:中国大陆
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T4065Fluorescein SodiumFluorescein Sodium,Fluorescein,inhibit,fluorescent probes,Inhibitor,tumor,Uranine,
Fluorescein Sodium is a phthalic indicator dye. It is used therapeutically as a diagnostic aid in corneal injuries and corneal trauma.
价 格:¥电议型 号:T4065产 地:中国大陆
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T20490NSC-120011
NSC-120011 can be used in the assay to screen proteolytic activities in mite homogenates.
价 格:¥电议型 号:T20490产 地:中国大陆
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T6501Fludarabine PhosphateNSC 118218,Fludarabine Phosphate,Inhibitor,Fludarabine,inhibit,NSC118218,Nucleo
Fludarabine Phosphate is the phosphate salt of a fluorinated nucleotide antimetabolite analog of the antiviral agent vidarabine (ara-A) with antineoplastic activity. Fludarabine phosphate is rapidly dephosphorylated to 2-fluoro-ara-A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2-fluoro-ara-ATP. This metabolite may inhibit DNA polymerase alpha, ribonucleotide reductase, and DNA primase, thereby interrupting DNA synthesis and inhibiting tumor cell gr
价 格:¥电议型 号:T6501产 地:中国大陆
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T6479Dovitinib lactate hydrateVEGFR1,FGFR1,TKI258 lactate,SCFR,CD117,Dovitinib lactate hydrate,FGFR,Fms l
Dovitinib (TKI258) Lactate is the Lactate of Dovitinib, which is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit) with IC50 of 1 nM/2 nM, also potent to class IV (FGFR1/3) and class V (VEGFR1-4) RTKs with IC50 of 8-13 nM, less potent to InsR, EGFR, c-Met, EphA2, Tie2, IGFR1 and HER2. Phase 4.
价 格:¥电议型 号:T6479产 地:中国大陆