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产品数：86101
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T9698UC2288Attenuator,786-O,Inhibitor,UC-2288,MDM-2/p53,inhibit,UC2288,ovarian,RCC,HK2,UC 2288,p21,sorafe
UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.
价 格：￥电议型 号：T9698产 地：中国大陆
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T7700LersivirineHIV,non-nucleoside reverse transcription,Reverse Transcriptase,HIV virus,UK 453061,Inhibi
Lersivirine(UK 453061) is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) under development for HIV infection therapy.
价 格：￥电议型 号：T7700产 地：中国大陆
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T8554KCC-07KCC07,BAI1,p53,inhibit,ADGRB1,anticancer,Inhibitor,DNA Alkylator/Crosslinker,MBD2,KCC-07,anti-
KCC-07 is a selective, potent and brain-penetrant inhibitor of methyl-CpG-binding domain protein 2(MBD2) with anticancer activity. KCC-07 prevents binding of MBD2 to methylated DNA and activates brain specific angiogenesis inhibitor 1 (BAI1) inducing anti-proliferative BAI1/p53/p21 signaling.
价 格：￥电议型 号：T8554产 地：中国大陆
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T26704AZ13705339
AZ13705339 is an effective inhibitor of PAK1 with an IC50 of 0.33 nM and a Kd of 0.28 nM. AZ13705339 binds PAK2 with a Kd of 0.32 nM. AZ13705339 can be used in studies about cancers.
价 格：￥电议型 号：T26704产 地：中国大陆
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TN1353N-BenzyllinoleamideNBenzyllinoleamide,energy,antioxidant,pharmaceutical,metabolism,N Benzyllinoleami
N-Benzyllinoleamide is a natural product isolated from Lepidium meyenii Walp, has pharmaceutical property against exercise-induced fatigue.
价 格：￥电议型 号：TN1353产 地：中国大陆
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T7318Elimusertibresponse,damage,ATM/ATR,stress,Inhibitor,BAY1895344,tumors,DNA,instability,lymphomas,inhi
BAY 1895344 is a potent, highly selective and orally available ATR inhibitor with an IC50 of 7 nM.BAY 1895344 shows potent anti-tumor efficacy in monotherapy and strong combination potential with the targeted alpha therapy Radium-223 dichloride.
价 格：￥电议型 号：T7318产 地：中国大陆
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T63534PPTN hydrochloride
PPTN hydrochloride is a potent, high-affinity, competitive, highly selective P2Y14 receptor antagonist (KB: 434 pM), but no agonist or antagonist activity at P2Y1, P2Y2, P2Y4, P2Y6, P2Y11, P2Y12 or P2Y13 receptors, exhibiting anti-inflammatory and anti-immune effects.
价 格：￥电议型 号：T63534产 地：中国大陆
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T6933PeficitinibJAK,Janus kinase,lymphocytes,JNJ 54781532,Peficitinib,JNJ54781532,Inhibitor,rheumatoid ar
Peficitinib (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3.
价 格：￥电议型 号：T6933产 地：中国大陆
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T100535HT6-ligand-15HT6 ligand 1,5HT-6-ligand-1,5HT6ligand1
5HT6-ligand-1 is an orally active ligand of 5-HT6 receptor (Ki = 1.43 nM).
价 格：￥电议型 号：T10053产 地：中国大陆
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T5530Mithramycin A
Mithramycin A, a DNA-binding antitumor antibiotic, is a selective specificity protein 1 (Sp1) inhibitor, which inhibits the growth of various cancers by decreasing Sp1 protein. Specificity protein 1 (Sp1) is a zinc-finger transcription factor that regulates multiple cellular functions and promotes tumor progression.
价 格：￥电议型 号：T5530产 地：中国大陆
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T9253CPFX4158CPFX4158,CPFX-4158
CPFX4158 is a mannose deriviative and an antibacterial agent that is potentially useful in transgenic humanized- CEACAM6 mouse.
价 格：￥电议型 号：T9253产 地：中国大陆
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T6538Hydroxypropyl CelluloseHydroxypropyl Cellulose
Hydroxypropyl cellulose (HPC) is a derivative of cellulose with both water solubility and organic solubility, it is used as food additive and sieving matrix for DNA separations.
价 格：￥电议型 号：T6538产 地：中国大陆
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T8053N-Acetyl-L-arginineInhibitor,N Acetyl L arginine,NAcetylLarginine,inhibit,Endogenous Metabolite
N-a-Acetyl-L-arginine, also known as N-ac-L-arg-OH or N-alpha-acetylarginine, belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. N-a-Acetyl-L-arginine serum levels (and other guanidino compounds) were elevated of all the hyperargininemic patients are higher than the normal range. N-a-Acetyl-L-arginine is a very strong basic compound (based on its pKa). Untreated hyperargini
价 格：￥电议型 号：T8053产 地：中国大陆
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T8657KYP-2047eNOS,inhibit,POP,Neurotensin,Angiopoietins,MDM-2/p53,KYP 2047,prolyl oligopeptidase,Glioblas
KYP-2047 is a very potent, selective Prolyl oligopeptidase (POP) inhibitor.
价 格：￥电议型 号：T8657产 地：中国大陆
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T216531,4-DPCAHIF-PH,HIF/HIF Prolyl-Hydroxylase,HIF-1α,HIFs,FIH,P4HA1,P4HA2,1,4DPCA,healing,Inhibitor,Hypo
1,4-DPCA is an inhibitor of prolyl-hydroxylase with an IC50 of 2.4 ?M for collagen hydroxylation in human foreskin fibroblasts and 60 μM for factor inhibiting HIF (FIH).
价 格：￥电议型 号：T21653产 地：中国大陆
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T15372GB1107
GB1107 is an effective and selective Galectin-3 inhibitor with a Kd of 37 nM.
价 格：￥电议型 号：T15372产 地：中国大陆
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T7539O6-Benzylguaninepancreatic,DNA/RNA Synthesis,transcriptional,PARP1,p53,inhibit,cyclin,O-6-Benzylguan
O6-Benzylguanine is a guanine analog with antineoplastic activity,and is a potent O6-alkylguanine DNA alkyltransferase (AGT) inactivator.
价 格：￥电议型 号：T7539产 地：中国大陆
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T16535PicrotoxininPicrotoxinin
Picrotoxinin is a blocker of chloride channel and a noncompetitive antagonist of GABAA with an IC50 of 1.15 μM for α1β2γ2L GABAA. Picrotoxinin shows convulsant properties.
价 格：￥电议型 号：T16535产 地：中国大陆
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T12753RORγt Inverse agonist 6Inhibitor,ROR,RORγt Inverse agonist-6,inhibit,RAR-related orphan receptor,ROR
RORγt Inverse agonist 6 is an agonist of RORγt inverse. RORγt Inverse agonist 6 can be used in research on Th17-driven autoimmune diseases.
价 格：￥电议型 号：T12753产 地：中国大陆
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T8535GAK inhibitor 49NAK,selective,GAK inhibitor-49,GAK inhibitor49,GAK inhibitor 49,Inhibitor,inhibit,AT
GAK inhibitor 49 is a highly selective and ATP-competitive cyclin G associated kinase (GAK) inhibitor (IC50: 56 nM; Ki: 0.54 nM ).
价 格：￥电议型 号：T8535产 地：中国大陆
