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Cat. No. Product Name Field of Application Chemical Structure
DCC1047 BMS-182874 Hydrochloride
Quantity (mg or Unit) Unit Price ($/mg or $/Unit) Final Price 100 $13.95 Total: $1,395.00 50 $16.12 Total: $806.00 25 $18.91 Total: $472.75 10 $22.32 Total: $223.20 5 $26.35 Total: $131.75
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DCC1046 Bms-181184
Novel antifungal and fungicidal agent
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DCC1045 bms-180448
Novel K channel opener; Glyburide-Reversible Cardioprotective Agent with Minimal Vasodilator Activity
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DCC1044 Bms-180048 Fumarate
5HT1B/1D agonist
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DCC1043 Bms-124110
Novel potent, selective inhibitor of AAK1 (adaptor associated kinase 1), having the appropriate combination of solubility and charge required for microiontophoresis
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DCC1042 Bms1018
Novel PD-1/PD-L1 Inhibitor
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DCC1041 Bms-1016
Novel PD-L1 Inhibitor
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DCC1040 Bmppb-32
Novel Highly Selective LRRK2 Inhibitor
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DCC1039 Bmp Activator B75
Novel activator of BMP signaling, enhancing osteoblast differentiation, targeting HECT domain of ubiquitin ligase Smurf1, up-regulating the protein level of Smad1/5
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DCC1038 Bmp Activator B06
Novel activator of BMP signaling, enhancing osteoblast differentiation, targeting HECT domain of ubiquitin ligase Smurf1, up-regulating the protein level of Smad1/5
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DCC1037 Bml277 Acid
Metabolite of BML277 which is a selective checkpoint kinase 2 inhibitor
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DCC1036 bml-259
Potent and selective inhibitor of Cdk5/p25, protecting large population of cells against non-A
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DCC1035 Bmi-1026
Novel potent cyclin-dependent kinases (CDK) inhibitor, inducing a strong cell cycle alteration
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DCC1034 Bmh-22
Novel inhibitor of RNA polymerase I, causing nucleolar stress and showing potent anticancer activity across many tumor types
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DCC1033 Bmd4503-2
Novel LRP5/6-sclerostin interaction inhibitor, recovering the downregulated activity of the Wnt/β-catenin signaling pathway by competitive binding to the LRP5/6-sclerostin complex
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DCC1032 Bmc201725-9o
Novel potent EGFR inhibitor
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DCC1031 Bm-573
Dual thromboxane synthase inhibitor and thromboxane receptor antagonist
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DCC1030 Bm-520
Original TXA2 modulator, inhibiting the action of thromboxane A2 and 8-iso-prostaglandin F2alpha
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DCC1029 Azaguanine-8
Inhibitor of Marburg virus (MARV) growth at noncytotoxic concentrations
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DCC1028 Calpain Inhibitor Ii
Inhibitor of calpain, cathepsin L and cathepsin B
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DCC1027 Bl-ei001
Novel ERK inhibitor, inducing breast cancer cell apoptosis via mitochondrial pathway but independent on Ras/Raf/MEK pathway
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DCC1026 Blapsin B
Potent 14-3-3 inhibitor
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DCC1025 Blapsin A
Natural Potent 14-3-3 inhibitor
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DCC1024 Blancoxanthone
Natural anti-coronavirus agent
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DCC1023 Bkm-570
Bradykinin antagonist, causing impressive growth inhibition of lung and prostate tumors, displaying superior in vivo inhibitory effects than convential chemotherapeutic drugs
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DCC1022 Bkm1972
Novel inhibitor of the expression of anti-apoptotic protein survivin and membrane-bound efflux pump ATP binding cassette B 1 (ABCB1, p-glycoprotein), presumably via signal transducer and activator of transcription 3 (Stat3), inhibiting human prostate canc
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DCC1021 Bkm1740
Novel effective inhibitor of survivin expression at both the mRNA and protein levels in vitro, significantly reducing survivin in bone metastatic C4-2 tumors
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DCC1020 Bkm1644
Novel inhibitor of survivin transcription through a signal transducer and activator of transcription 3 (Stat3)-dependent mechanism, inhibiting tissue expression of survivin and inducing apoptosis in C4-2 skeletal tumor
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DCC1019 Bki-1814
Novel potent and selective bumped kinase inhibitor (BKI) CpCDPK1 IC 50 0.005 µM
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DCC1018 Bki-1812
Novel potent and selective bumped kinase inhibitor (BKI) CpCDPK1 IC 50 0.0025 µM
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