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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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