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产品数：86101
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T9374AA38-3serine,ABHD6,Fatty acid amide hydrolase,AA38 3,Monoacylglycerol lipase,AA383,ABHD11,FAAH,MAGL,
AA38-3 inhibites three SHs (ABHD6, ABHD11, and FAAH)
价 格：￥电议型 号：T9374产 地：中国大陆
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T10269AHR antagonist 2AHR antagonist 2
AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.
价 格：￥电议型 号：T10269产 地：中国大陆
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T6703Tetrahydrozoline hydrochloridecongestion,conjunctival,Beta Receptor,Tetryzoline,Tetrahydrozoline hyd
Tetrahydrozoline HCl is an imidazoline derivative with alpha receptor agonist activity.
价 格：￥电议型 号：T6703产 地：中国大陆
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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
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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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T60193CB-53391HIndole4carboxamide,2methyl1[5,6,7,8tetrahydro4[(phenylmethyl)amino]pyrido[2,3d]pyrimidin2yl
p97-IN-1 is a potent inhibitor of p97 with an IC 50 <30 nM [1].
价 格：￥电议型 号：T60193产 地：中国大陆
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T8900SeralutinibPK 10571,Seralutinib,inhibit,arterial,PDGFR,PK10571,PK-10571,PAH,Pulmonary,hypertension,G
Seralutinib is an inhibitor of inhaled PDGFRα and PDGFRβ. It is used in the study for pulmonary arterial hypertension.
价 格：￥电议型 号：T8900产 地：中国大陆
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T6652Salbutamol hemisulfateAdrenergic Receptor,Beta Receptor,Inhibitor,Salbutamol hemisulfate,AH-3365 hem
Salbutamol Sulfate is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 μM.
价 格：￥电议型 号：T6652产 地：中国大陆
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T67836AT-533Benzamide,2[(trans4hydroxycyclohexyl)amino]4(4,5,6,7tetrahydro3,6,6trimethyl4oxo1Hindazol1yl)
AT-533 is a potent inhibitor of Hsp90 and HSV. AT-533 blocks the HIF-1α/VEGF/VEGFR-2 signaling pathway, leading to suppress tumor growth and angiogenesis. AT-533 also inhibits the activation of the downstream pathways, including Erk1/2, FAK, Akt/mTOR/p70S6K,. AT-533 inhibits the cell migration, invasion, and the tube formation of human umbilical vein endothelial cells (HUVECs).
价 格：￥电议型 号：T67836产 地：中国大陆
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T9943(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid(E)6(4methylbenzyli
(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid is a 2-?benzylidene tetrahydronaphthone derivative and can be used as a firefly luciferase inhibitor in kit.
价 格：￥电议型 号：T9943产 地：中国大陆
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T12262L1NPS ALX Compound 4a hydrochloride(1:1)NPSALXCompound4ahydrochloride(299433106Freebase)
NPS ALX Compound 4a hydrochloride(1:1) is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM.
价 格：￥电议型 号：T12262L1产 地：中国大陆
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T80502-Methyltetrahydrofuran-3-oneInhibitor,2Methyltetrahydrofuran3one,2 Methyltetrahydrofuran 3 one,inhi
2-Methyltetrahydrofuran-3-one, also known as fema 3373 or tetrahydro-2-methyl-3-furanone, belongs to the class of organic compounds known as furanones.
价 格：￥电议型 号：T8050产 地：中国大陆
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T643631-Pentalenol, 5-hexyl-1,2,3,3a,6,6a-hexahydro-4-phenyl-3a-(1-phenylethenyl)-, (1R,3aS,6aS)-rel-1Pent
1-Pentalenol, 5-hexyl-1,2,3,3a,6,6a-hexahydro-4-phenyl-3a-(1-phenylethenyl)-, (1R,3aS,6aS)-rel- is a potent liver receptor homolog 1 (LRH-1, NR5A2) and steroidogenic factor-1 (SF-1, NR5A1) agonist with pEC 50 s of 6.4 and 7.2, respectively.
价 格：￥电议型 号：T64363产 地：中国大陆
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TN1451Brevifolincarboxylic acidGlucosidase,AhR,Brevifolincarboxylic acid,Inhibitor,Aryl Hydrocarbon Recept
Brevifolincarboxylic acid is a natural product isolated from Polygonum capitatum, it has inhibitory effect on the aryl hydrocarbon receptor (AhR). Brevifolincarboxylic acid is an α-glucosidase inhibitor with an IC50 of 323.46 μM.
价 格：￥电议型 号：TN1451产 地：中国大陆
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T7730AminopterinAminopterin,tetrahydrofolic,inhibit,anticancer,immunosuppressive,acid,Antifolate,leukocyt
Aminopterin is a synthetic folic acid derivative whose metabolite is a competitive inhibitor of dihydrofolate reductase
价 格：￥电议型 号：T7730产 地：中国大陆
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T9800Cyclopenta[c][1]benzopyran-8-ol, 1,2,3,3a,4,9b-hexahydro-4-(4-hydroxyphenyl)-, (3aR,4S,9bS)-rel-Cycl
Cyclopenta[c][1]benzopyran-8-ol, 1,2,3,3a,4,9b-hexahydro-4-(4-hydroxyphenyl)-, (3aR,4S,9bS)-rel- is an estrogen receptor beta (ERβ) agonist.
价 格：￥电议型 号：T9800产 地：中国大陆
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TN10841,3,5,8-TetrahydroxyxanthoneInhibitor,colitis,anti-inflammatory,muscle,inhibit,1,3,5,8-Tetrahydroxyx
Desmethylbellidifolin is a natural xanthone extracted from Gentianella acuta. 1,3,5,8-Tetrahydroxyxanthone has antispasmodic effect and anti-inflammatory activity. Dimethylbellidifolin shows mutagenicity in Salmonella typhimurium TA100, TA98, TA97, and TA2637 by the preincubation method; it also exhibits at the dose of 200 ug/disk a significant inhibition of the growth of Staphylococcus aureus.
价 格：￥电议型 号：TN1084产 地：中国大陆
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T7752(S,R,S)-AHPC-MeVHL ligand-2,VHL ligand2,Inhibitor,inhibit,Ligands for E3 Ligase,(S,R,S) AHPC Me,(S,R
(S,R,S)-AHPC-Me (VHL ligand 2) is the (S,R,S)-AHPC-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein[1]. (S,R,S)-AHPC-Me can be used to synthesize ARV-771. ARV-771 is a von Hippel-Landau (VHL) E3 ligase-based BET PROTAC degrader. ARV-771 potently degrades BET protein in castration-resistant prostate cancer (CRPC) cells with a DC50 <1 nM.
价 格：￥电议型 号：T7752产 地：中国大陆
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TP1426His-[D-2-ME-Trp]-AlaHis[D2METrp]Ala,His [D 2 ME Trp] Ala
His-[D-2-ME-Trp]-Ala is a peptide fragment of the growth hormone hexarelin.
价 格：￥电议型 号：TP1426产 地：中国大陆
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T8187TetrahydroepiberberineFungal,Influenza Virus,inhibit,Inhibitor,antifungal,PI-3,impatiens,alkaloid,Te
Tetrahydroepiberberine, an isoquinoline alkaloid, has antifungal and selective inhibition against the PI-3 virus activities.
价 格：￥电议型 号：T8187产 地：中国大陆
