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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC65053 | 1,2-Hydrazinedicarboxylic acid, 1-(4-fluoro-3,5-dimethylphenyl)-, 1,2-bis(1,1-dimethylethyl) ester Featured |
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| DC65051 | 2-Phenyl-1H-pyrrolo[2,3-b]pyridin-5-amine Featured |
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| DC65049 | 5-Bromo-4-fluoro-1-methylindazole Featured |
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| DC65048 | Temanogrel Featured |
Temanogrel is a highly selective 5-HT2A receptor antagonist with a Ki of 4.9 nM.
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| DC65042 | Methyl 3-(methoxymethyl)-1H-pyrazole-4-carboxylate Featured |
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| DC65041 | Ethyl 5-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-1H-indole-2-carboxylate Featured |
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| DC65040 | CAL-130 Racemate Featured |
CAL-130 Racemate is the racemate of CAL-130. CAL-130 Racemate is a PI3Kδ inhibitor.
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| DC65039 | Benzo[b][1,6]naphthyridine-4-carbonitrile, 3-chloro- Featured |
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| DC65038 | 5-Pyrimidinecarbonitrile,6-[2-(dimethylamino)ethenyl]-1,4-dihydro-4-oxo-1-phenyl- Featured |
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| DC65037 | 2-AMINO-6-METHYL-N-O-TOLYLBENZAMIDE Featured |
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| DC65015 | m-PEG10-CH2COOH Featured |
m-PEG10-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
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| DC65014 | m-PEG8-CH2COOH Featured |
m-PEG8-CH2COOH is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.
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| DC65013 | m-PEG6-CH2COOH Featured |
m-PEG6-O-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
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| DC65012 | m-PEG4-CH2COOH Featured |
m-PEG4-CH2COOH is a PEG-based based PROTAC linker can be used in the synthesis of PROTACs.
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| DC65011 | m-PEG3-CH2COOH Featured |
m-PEG3-CH2COOH is a PEG-based based PROTAC linker can be used in the synthesis of PROTACs.
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| DC65010 | m-PEG11-alcohol Featured |
m-PEG11-alcohol is a PEG derivative containing a hydroxyl group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The hydrophilic PEG spacer increases solubility in aqueous media.
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| DC65022 | 1,2,5-Oxadithiolane, 2,2,5,5-tetraoxide Featured |
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| DC65024 | CPI-455 HCl Featured |
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| DC65027 | 9H-Purin-6-amine, 2-chloro-N-[(4,6-dimethyl-3-pyridinyl)methyl]-9-(1-methylethyl)- Featured |
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| DC65026 | 1H-Phenalene Featured |
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| DC65029 | Vactosertib HCl Featured |
Vactosertib Hydrochloride (EW-7197 Hydrochloride) is a small-molecule ATP-competitive inhibitor of TGFβRI (ALK5) with an IC50 of 12.9 nM.
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| DC65030 | Benzoic acid, 2-(2,2,2-trifluoro-1-methylethyl)hydrazide Featured |
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| DC65031 | 1-(1,1,1-trifluoropropan-2-yl)hydrazine Featured |
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| DC70866 | UHRF1 PHD inhibitor MLD5 |
UHRF1 PHD inhibitor MLD5 is a specific compound that selectively inhibits the UHRF1-histone interaction (IC50=7.4 uM), targets the PHD finger of UHRF1, specifically disrupting histone H3 arginine 2 interactions with the PHD finger.UHRF1 PHD inhibitor MLD5 inhibited binding between H3K9me3(FAM) and UHRF1 with IC50 of 24-26 uM, displace UHRF1-histone H3 binding in cells.
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| DC70865 | UHRF1 PHD inhibitor MLD4 Featured |
UHRF1 PHD inhibitor MLD4 is a specific compound that selectively inhibits the UHRF1-histone interaction (IC50=12.4 uM), targets the PHD finger of UHRF1, specifically disrupting histone H3 arginine 2 interactions with the PHD finger.UHRF1 PHD inhibitor MLD4 inhibited binding between H3K9me3(FAM) and UHRF1 with IC50 of 24-26 uM, displace UHRF1-histone H3 binding in cells.
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| DC70653 | NJH-2-075 Featured |
NJH-2-075 is an alkyne-functionalized probe of EN523, retains binding to OTUB1 in vitro.
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| DC12578 | IMTPPE Featured |
IMTPPE (SID3712502) is a novel small molecule capable of inhibiting androgen receptor (AR) transcriptional activity (IC50=1 uM) and protein level in C4-2 prostate cancer cells.
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| DC28412 | m-PEG5-CH2COOH Featured |
m-PEG5-CH2COOH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
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| DC65006 | Metasilicic acid Featured |
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| DC65005 | Diuron Featured |
Diuron is a phenylurea herbicide that inhibits photosynthesis by preventing the formation of ATP and NADH. Diuron (2,500 ppm, dietary) increases the incidence of urinary bladder urothelial carcinomas in male and female mice by 73 and 27%, respectively.
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