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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
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T6420BMS-707035BMS 707035,HIV-1 integrase strand transfer,HIV,Human immunodeficiency virus,antiviral,BMS7
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：中国大陆
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T7652AM211inhibit,AM211,Inhibitor,Prostaglandin Receptor,AM 211,AM-211
AM211 is a potent and orally bioavailable antagonist of prostaglandin D2 (PGD2) receptor type 2 (DP2)
价 格：￥电议型 号：T7652产 地：中国大陆
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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
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T21012DiflufenicanDiflufenican
Diflufenican increases the production of phytoene in carrot cell cultures by inducing the inhibition of phytoene desaturase gene expression.
价 格：￥电议型 号：T21012产 地：中国大陆
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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
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TQ01353,4-Dihydroxymandelic acid3,4-Dihydroxymandelic acid,inhibit,Endogenous Metabolite,3,4Dihydroxymande
3,4-Dihydroxymandelic acid exists in all living organisms, ranging from bacteria to humans. Within humans, 3,4-dihydroxymandelic acid participates in a number of enzymatic reactions. 3,4-Dihydroxymandelic acid is a metabolite of norepinephrine.
价 格：￥电议型 号：TQ0135产 地：中国大陆
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T6S1917Schisandrol BTJN 101,antioxidant,Hepato-protective,BCL-2,TJN101,inhibit,P-glycoprotein,Inhibitor,CYP
1. Gomisin A may exert neuroprotective effects by attenuating the microglia-mediated neuroinflammatory response via inhibiting the TLR4-mediated NF-κB and MAPKs signaling pathways. 2. Gomisin A has anti-inflammatory property, potentially result from the inhibition of COX-2, iNOS, IL-6, TNF-α and NO through the down-regulation of RIP2 and NF-κB activation. 3. Gomisin A induces marked protective effects against hepatic and renal injury induced by CCl(4) exposure through differential regulation of
价 格：￥电议型 号：T6S1917产 地：中国大陆
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T9625SandaloreInhibitor,Apoptosis,Sandalore,IGF-1,spontaneous,olfactory receptor,hair growth,inhibit,foll
Sandalore prolongs human hair growth by decreasing apoptosis and increasing the production of the anagen-prolonging growth factor IGF-1 in the outer root sheath. Sandalore is a selective agonist of olfactory receptor OR2AT4.
价 格：￥电议型 号：T9625产 地：中国大陆
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T6665Sertaconazole nitrateCOX-2,Inhibitor,inhibit,Sertaconazole nitrate,MCF-7,HaCaT,Candida,HeLa,p38 MAPK
Sertaconazole nitrate, a topical broad-spectrum antifungal, is developed to supply an additional agent for the treatment of superficial cutaneous and mucosal infections.
价 格：￥电议型 号：T6665产 地：中国大陆
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T7755Thalidomide 4-fluorideCereblon ligand-4,inhibit,Cereblon ligand4,Thalidomide 4-fluoride,Thalidomide
Thalidomide 4-fluoride (Cereblon ligand 4) is the Thalidomide-based Cereblon ligand. Thalidomide 4-fluoride can be used in the recruitment of CRBN protein. Thalidomide 4-fluoride (Cereblon ligand 4) can be connected to the ligand for IRAK4 protein by a linker to form PROTAC IRAK4 degrader-1.
价 格：￥电议型 号：T7755产 地：中国大陆
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T6S2384PoliumosidePoliumoside,RLAR,AGE,Aldose Reductase,Inhibitor,aldose,advanced,glycation,product,Brandis
Poliumoside is a natural compound which exhibits significant inhibition of advanced glycation end product formation with IC50 value of 4.6-25.7 μM, it also exhibits great inhibitory effects on rat lens aldose reductase with IC50 values of 0.85 μM.Poliumoside has oxidant scavenging, antibacterial and hemostasis capacities, it can inhibit Biofilm-forming Staphylococcus aureus in mice.
价 格：￥电议型 号：T6S2384产 地：中国大陆
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T9168NSC 617145NSC 617145,breaks,NHEJ,helicase,DSB,abnormalities,WRN,DNA/RNA Synthesis,strand,Rad51,chrom
NSC617145 is an inhibitor of WRN helicase that inhibits the ATPase, but not exonuclease, activity of WRN helicase in a concentration-dependent manner.
价 格：￥电议型 号：T9168产 地：中国大陆
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T18640(S,R,S)-AHPC-C4-NH2 hydrochlorideinhibit,E3 Ligase Ligand-Linker Conjugates,(S,R,S)AHPCC4NH2 hydroch
(S,R,S)-AHPC-C4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate incorporating the (S,R,S)-AHPC based VHL ligand and a linker.
价 格：￥电议型 号：T18640产 地：中国大陆
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T8208androsinInhibitor,inhibit,androsin
Androsin, isolated from Picrorhiza Kurroa Royle ex Benth, has anti-asthmatic effects.
价 格：￥电议型 号：T8208产 地：中国大陆
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T12551PROTAC BRD4 ligand-1PROTAC BRD4 ligand 1,PROTAC BRD4 ligand1,PROTAC BRD-4 ligand-1
PROTAC BRD4 ligand-1 is a ligand for BRD4 for Protac GNE-987 and an inhibitor of BET.
价 格：￥电议型 号：T12551产 地：中国大陆
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T6859I-BRD9cancer,inhibit,Epigenetic Reader Domain,bromodomain-containing protein 7(BRD7),bromodomain and
I-BRD9 is the first selective cellular inhibitor for BRD9 with pIC50 of 7.3.
价 格：￥电议型 号：T6859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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T8412(S,R,S)-AHPCInhibitor,inhibit,(S,R,S)AHPC,E3 ligase-recruiting Moiety,Ligands for E3 Ligase,(S,R,S)-
MDK7526 is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC is potential useful for the targeted degradation of the androgen receptor.
价 格：￥电议型 号：T8412产 地：中国大陆
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T60015TSPO ligand-2?TSPO ligand-2,Inhibitor,TSPO ligand 2,Autophagy-targeting chimeras,AUTACs,inhibit,TSPO
TSPO ligand-2 is a ligand of AUTAC1 which contains a p-fluorobenzylguanine and a Fumagillol moiety.
价 格：￥电议型 号：T60015产 地：中国大陆
