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T21083TFIIH Modulator-19；化合物TFIIH Modulator-19TFIIH Modulator19|||TFIIH Modulator 19；TFIIH Modulator19|||T
TFIIH Modulator-19 induces the dimerization of trichothiodystrophy group A protein to modulate TFIIH transcriptional activity.
价 格：￥电议型 号：T21083产 地：中国大陆
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T210822,5-Dihydroxybiphenyl；2,5-二羟基联苯TFIIH Modulator 12|||TFIIH Modulator12；TFIIH Modulator 12|||2,5-二羟基联苯
2,5-Dihydroxybiphenyl (TFIIH Modulator12), a small molecule destabilization inducer, induces the dimerization of trichothiodystrophy group A protein to modulate TFIIH transcriptional activity.
价 格：￥电议型 号：T21082产 地：中国大陆
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T21081Chlortetracycline；氯四环素Biomycin|||Chlormax|||7-Chlorotetracycline|||Acronize|||Aureomycin|||Aureomyci
Chlortetracycline is a broad-spectrum antibiotic tetracycline with a 7-chloro substitution. It inhibits growth of both Gram-negative and Gram-positive bacteria by inhibiting protein synthesis.
价 格：￥电议型 号：T21081产 地：中国大陆
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T21080(3S,5S)-Atorvastatin(3S,5S)-阿托伐他汀ent-Atorvastatin|||3S,5S-Atorvastatin|||(3S,5S)-阿托伐他汀
ent-Atorvastatin is a selective and competitive inhibitor of HMGCR (HMG-CoA reductase).
价 格：￥电议型 号：T21080产 地：中国大陆
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T20788Empenthrin；化合物 T20788MA-108|||S2852|||S 2852|||MA108|||S-2852|||MA 108；MA-108|||S2852|||S 2852|||MA1
Empenthrin, a synthetic pyrethroid used in insecticides, is active against broad spectrum of flying insects including moths and other pests damaging textile.
价 格：￥电议型 号：T20788产 地：中国大陆
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T20785Terallethrin；化合物 T20785M-108|||M 108|||M108|||Knockthrin；M-108|||M 108|||M108|||Knockthrin
Terallethrin, a pesticide, controls flying insects including houseflies, mosquitoes, and wasps.
价 格：￥电议型 号：T20785产 地：中国大陆
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T20565Pseudoakuammigine；化合物 T20565NSC381082|||NSC 381082|||NSC-381082；NSC381082|||NSC 381082|||NSC-381082
Pseudoakuammigine is a biochemical substance.
价 格：￥电议型 号：T20565产 地：中国大陆
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T20535Carnidazole；卡硝唑ME 108|||NSC293873|||NSC 293873|||ME-108|||NSC-293873|||ME108；ME 108|||NSC293873|||NS
Carnidazole (ME-108) shows antiprotozoal activity and can be used in studies about the treatment of Trichomonas infection.
价 格：￥电议型 号：T20535产 地：中国大陆
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T2038RG108；化合物RG108N-Phthalyl-L-tryptophan；N-Phthalyl-L-tryptophan
RG108 (N-Phthalyl-L-tryptophan) is an DNA methyltransferase inhibitor(IC50=115 nM).
价 格：￥电议型 号：T2038产 地：中国大陆
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T19559Seocalcitol；化合物 T19559EB 1089；EB 1089
Seocalcitol is an analog of vitamin D, binds vitamin D receptor protein from human osteosarcoma MG-63 cells(Kd : 0.27 nM).
价 格：￥电议型 号：T19559产 地：中国大陆
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T19214Bredinin aglycone；5-羟基-1H-咪唑-4-甲酰胺5-Hydroxy-1H-imidazole-4-carboxamide|||SM-108；5-Hydroxy-1H-imidazo
Bredinin aglycone (SM-108) is a purine nucleotide analog. It can be used to examine the efficiency of catalysts for the preparation of purine nucleotide analogs.
价 格：￥电议型 号：T19214产 地：中国大陆
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T1910824, 25-Dihydroxy VD324,25-二羟基维生素 D324,25-二羟基维生素 D3
24, 25-Dihydroxy VD3 is closely related to 1,25-dihydroxy vitamin D3, the active form of vitamin D3.
价 格：￥电议型 号：T19108产 地：中国大陆
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T18108m-PEG-thiol (MW 10000)；化合物 T18108m-PEG-thiol (MW 10000)
m-PEG-thiol (MW 10000) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T18108产 地：中国大陆
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T1741AZD1080；化合物AZD1080AZD1080
AZD1080 is a selective, orally active, brain permeable GSK3 inhibitor.
价 格：￥电议型 号：T1741产 地：中国大陆
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T17108TMP920；化合物 T17108TMP920
TMP920 inhibits RORγt binding to the SRC1 peptide (IC50: 0.03 μM). TMP920 is a highly potent and selective RORγt antagonist.
价 格：￥电议型 号：T17108产 地：中国大陆
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T16521Phenglutarimid；化合物 T16521Phenglutarimide|||Ciba 10870；Phenglutarimide|||Ciba 10870
Phenglutarimid is an anticholinergic. It is used as an antiparkinsonian agent.
价 格：￥电议型 号：T16521产 地：中国大陆
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T16514PF 04531083；化合物PF 04531083PF 04531083
PF 04531083 is a selective blocker of the NaV1.8 channel. PF 04531083 can be used for neuropathic and inflammatory pain studies.
价 格：￥电议型 号：T16514产 地：中国大陆
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T15805LLY2510924 acetate(1088715-84-7 free base)；化合物LY2510924 acetateLY2510924 acetate(1088715-84-7 free ba
Ly2510924 acetate is an potent and selective CXCR4 antagonist. It prevents the binding of SDF-1 to CXCR4 with an IC50 of 0.079 nM.
价 格：￥电议型 号：T15805L产 地：中国大陆
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T15108DG-041；化合物DG-041DG-041
DG-041 is an antagonist of high affinity EP3 receptor (IC50s: 4.6 nM and 8.1 nM in the binding and FLIPR assay, respectively ). DG-041 inhibits PGE2 facilitation of platelet aggregation and it also crosses the blood-brain barrier.
价 格：￥电议型 号：T15108产 地：中国大陆
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T15079DBPR108；化合物DBPR108DBPR108
DBPR108 is an orally bioavailable dipeptide-derived DPP4 inhibitor (IC50: 15 nM) and it has no inhibition on DDP8 and DPP9.
价 格：￥电议型 号：T15079产 地：中国大陆
