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T20141L-6355；化合物 T20141L-6355|||L 6355|||L 6355|||Demonoiodoamiodarone|||Demonoiodoamiodarone|||L6355|||Am
L-6355 is an agent of bioactive chemicals.
价 格：￥电议型 号：T20141产 地：中国大陆
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T18817Thalidomide-O-amido-C8-NH2 hydrochloride；化合物 T18817Thalidomide-O-amido-C8-NH2 hydrochloride (1950635
Thalidomide-O-amido-C8-NH2 hydrochloride is a synthetic conjugate of an E3 ligase ligand-linker, which combines a cereblon ligand derived from Thalidomide and a linker. It can be utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T18817产 地：中国大陆
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T18635PROTAC RAR Degrader-1；化合物 T18635PROTAC RAR Degrader-1
PROTAC RAR Degrader-1, an RAR degrader, consists of a cIAP1 ligand binding group, a linker, and an RAR ligand binding group. It achieves maximal RAR degradation at a concentration of 30 μM in HT1080 cells. Degradation inducers that utilize cIAP1 are known as specific and non-genetic IAP-dependent protein erasers (SNIPERs)[1].
价 格：￥电议型 号：T18635产 地：中国大陆
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T17635Bis-Tos-PEG6；化合物 T17635Bis-Tos-PEG6
Bis-Tos-PEG6 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：T17635产 地：中国大陆
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T16700QC6352化合物 T16700QC 6352|||QC6352|||QC-6352
QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).
价 格：￥电议型 号：T16700产 地：中国大陆
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T16635Propargyl-PEG4-Tos；化合物 T16635Propargyl-PEG4-Tos
Propargyl-PEG4-Tos is a PEG-based PROTAC linker utilized for the synthesis of PROTACs and cleavable ADC linkers in antibody-drug conjugate (ADC) synthesis [1][2].
价 格：￥电议型 号：T16635产 地：中国大陆
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T16359NU6140；化合物NU6140NU6140
NU6140 is a selective inhibitor of CDK2-cyclin A (IC50, 0.41 μM). It shows 10- to 36-fold selectivity over other CDKs. NU6140 also effectively inhibits Aurora A and Aurora B (IC50s: 67 and 35 nM, respectively). It also enhances the apoptotic effect and has anti-cancer activity.
价 格：￥电议型 号：T16359产 地：中国大陆
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T16358NTRC-824；化合物 T16358NTRC-824
NTRC-824 is >150-fold selectivity for NTS2 over NTS1 (Ki >30 μM). NTRC-824 is an effective, selective, and neurotensin-like nonpeptide neurotensin receptor type 2 (NTS2) antagonist (IC50: 38 nM and a Ki : 202 nM).
价 格：￥电议型 号：T16358产 地：中国大陆
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T16357DA-3003-1化合物 DA-3003-1NSC 663284
DA-3003-1 (DA-3003-1) is a membrane-permeable, potent and selective Cdc25 dual specificity phosphatase inhibitor with antitumor activity that inhibits Cdc25B2, Cdc25A, Cdc25B2 and Cdc25C.
价 格：￥电议型 号：T16357产 地：中国大陆
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T16356Glyoxalic acid化合物 T16356Oxalaldehydic acid|||NSC 27785|||Formylformic acid
Glyoxalic acid is an organic compound. It is both an aldehyde and a carboxylic acid.
价 格：￥电议型 号：T16356产 地：中国大陆
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T16355NSC781406；化合物NSC781406NSC781406
NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).
价 格：￥电议型 号：T16355产 地：中国大陆
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T16354NSC745885；化合物 T16354NSC745885
NSC745885 is an effective down-regulator of EZH2 via proteasome-mediated degradation. NSC745885 is also an effective anti-tumor agent that displays selective toxicity against multiple cancer cell lines but not normal cells. NSC745885 offers possibilities for the study of advanced bladder and oral squamous cell carcinoma (OSCC) cancers.
价 格：￥电议型 号：T16354产 地：中国大陆
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T16353Meseclazone；美西拉宗W2395|||NSC297623；美西拉宗|||W2395|||NSC297623
Meseclazone has anti-inflammatory, analgesic, and antipyretic activity. Meseclazone shows inhibitory potency of secondary phase ADP aggregation.
价 格：￥电议型 号：T16353产 地：中国大陆
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T16352NSC23925；化合物 T16352NSC23925
NSC23925 is a selective and effective inhibitor of P-glycoprotein (Pgp).
价 格：￥电议型 号：T16352产 地：中国大陆
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T16351NSC16168；化合物 T16351NSC16168
NSC16168 inhibits DNA repair and potentiates CDDP efficacy in cancer. NSC16168 is a specific ERCC1-XPF inhibitor (IC50: 0.42 μM).
价 格：￥电议型 号：T16351产 地：中国大陆
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T16350NSC-87877；化合物NSC-87877NSC-87877
NSC-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatases (IC50=0.318 μM, 0.355 μM of shp2 and shp1, respectively).It also inhibits dual-specificity phosphatase 26 (DUSP26).
价 格：￥电议型 号：T16350产 地：中国大陆
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T1635Fenchlorphos；皮蝇磷Ronnel|||Dermafos；Ronnel|||Dermafos|||皮蝇磷
Fenchlorphos (Dermafos) is a cholinesterase inhibitor, used as an insecticide.
价 格：￥电议型 号：T1635产 地：中国大陆
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T15635JZP-430；化合物JZP-430JZP-430
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
价 格：￥电议型 号：T15635产 地：中国大陆
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T14923Cefpiramide sodium头孢匹胺钠头孢匹胺钠|||SM-1652|||Wy-44635
Cefpiramide sodium (SM-1652; Wy-44635) is a Pseudomonas-active cephalosporin. It has a broad spectrum of antibacterial activity.
价 格：￥电议型 号：T14923产 地：中国大陆
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T14635Bis-PEG3-NHS ester；化合物Bis-PEG3-NHS esterBis-PEG3-NHS ester
Bis-PEG3-NHS ester is a nonclaevable 3-unit PEG linker used in antibody-drug-conjugation (ADC).
价 格：￥电议型 号：T14635产 地：中国大陆
