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产品数:86101
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TN2069PicrocrocinInhibitor,Picrocrocin,antiproliferative,SKMEL-2,Apoptosis,malignant,melanoma,cells,human,
Picrocrocin is a natural product
价 格:¥电议型 号:TN2069产 地:中国大陆
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T7015Vps34-IN-1inhibit,Autophagy,Vps34IN1,PI3K,Vps-34-IN-1,Inhibitor,Phosphoinositide 3-kinase,Vps34 IN 1
Vps34-IN1 is a potent and highly selective Vps34 inhibitor with IC50 of 25 nM invitro, which does not significantly inhibit the isoforms of class I as well as class II PI3Ks.
价 格:¥电议型 号:T7015产 地:中国大陆
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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
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T6815HS-1371HS-1371,Inhibitor,Receptor-interacting protein kinases,RIPK,inhibit,HS 1371,RIP kinase,HS1371
HS-1371 is a novel kinase inhibitor of receptor-interacting protein kinase 3 (RIP3) with an IC50 of 20.8 nM.
价 格:¥电议型 号:T6815产 地:中国大陆
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T8722iKIX1antifungal,Inhibitor,drug-resistant,Fungal,CgGal11A,CgPdr1,infection,C. glabrata,iKIX1,inhibit,
iKIX1 is an Pdr1-dependent gene activation. It re-sensitizes drug-resistant C. glabrata to azole antifungals in vitro and in animal models for disseminated and urinary tract C. glabrata infection.
价 格:¥电议型 号:T8722产 地:中国大陆
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T9100BP 897inhibit,BP-897,BP897,cocaine drug-seeking,BP 897,Dopamine Receptor,Inhibitor,addiction,behavio
2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]- is a potent and selective dopamine D3 receptor agonist, and a weak dopamine D2 receptor antagonist, with Kis of 0.92 nM and 61 nM for D3 and D2 receptors, and shows low affinities at D1 and D4 receptors (Kis, 3 and 0.3 μM, respectively).
价 格:¥电议型 号:T9100产 地:中国大陆
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T20688LLeucokinin I acetateLeucokinin I acetate
Leucokinin I acetate is an antiserum raised against an insect myotropic peptide.
价 格:¥电议型 号:T20688L产 地:中国大陆
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T9228Propionylpromazine hydrochloridePropiopromazine,Propionylpromazine,DRD2,Dopamine Receptor,Parkinson,
Propionylpromazine hydrochloride is a dopamine receptor D2 (DRD2) antagonist.
价 格:¥电议型 号:T9228产 地:中国大陆
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T8003Methotrexate disodiumDNA/RNA Synthesis,WR19039 disodium,DNA,leukemia,immunosuppressant,reductase,ADC
Methotrexate disodium is an tetrahydrofolate dehydrogenase inhibitor
价 格:¥电议型 号:T8003产 地:中国大陆
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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
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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
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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
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TJS0328Nordalberginpromyelocytic,Inhibitor,coumarin,HL-60,cells,leukemia,differentiation,Nordalbergin,inhib
价 格:¥电议型 号:TJS0328产 地:中国大陆
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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
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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
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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
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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
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T6883SamotolisibInhibitor,mTOR,LY-3023414,Phosphoinositide 3-kinase,DNA-dependent protein kinase,inhibit,
LY3023414 is an oral ATP competitive inhibitor of the class I PI3K isoforms, DNA-PK, and mTOR. LY3023414 has been used in trials studying the treatment of Neoplasm, Solid Tumor, COLON CANCER, BREAST CANCER, and Advanced Cancer, among others.
价 格:¥电议型 号:T6883产 地:中国大陆
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T6644RolipramHuman immunodeficiency virus,SB95952,Rolipram,ZK62711,Inhibitor,SB-95952,Bacterial,Phosphodi
Rolipram is a phosphodiesterase 4 inhibitor with antidepressant properties.
价 格:¥电议型 号:T6644产 地:中国大陆
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T6068MK-5108MK 5108,VX689,Aurora Kinase,VX 689,inhibit,Autophagy,MK-5108,Inhibitor
MK-5108 is a highly potent and specific Aurora-A kinase inhibitor with an IC50 value of 0.064 nM.
价 格:¥电议型 号:T6068产 地:中国大陆