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Cat. No. Product Name Field of Application Chemical Structure
DCC4001 Parogrelil
Novel potent phosphodiesterase 3 inhibitor, suppressing the asthmatic response and showing both bronchodilating and anti-inflammatory effects
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DCC4000 Paraquat Diiodide
Non-selective contact herbicide, killing green plant tissue on contact, being highly toxic and linked to Parkinson's disease, generating reactive oxygen species (ROS), which causes cell death and potentially leading to acute respiratory distress syndrome
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DCC3999 Paraoxon
Acetylcholinesterase inhibitor, the active metabolite of the insecticide parathion
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DCC3998 Para-nitroblebbistatin
Selective cell-permeable inhibitor of non-muscle myosin II ATPases, being more stable and less phototoxic than Blebbistatin
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DCC3997 Para-cid-5951923
Isomer of CID-5951923
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DCC3996 Para-aminoblebbistatin
Blebbistatin derivative, increasing water solubility, decreases the inherent fluorescence, stabilizing the molecule to circumvent its degradation by prolonged blue light exposure, and decreasing its phototoxicity while retaining the in vitro and in vivo a
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DCC3994 Pape-1
Pathway Preferential Estrogen, activating the extranuclear signaling pathway without activity on the nuclear signaling pathway
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DCC3993 Pao-pdt
Potent and highly selective small molecule inhibitor of thioredoxin reductase (TrxR)
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DCC3992 Pan-raf/rtk Inhibitor I-16
Novel potent pan-Raf and receptor tyrosine kinase inhibitor, potently inhibits all subtypes of Rafs with IC50 values of 3.49 (BRafV600E), 8.86 (ARaf), 5.78 (BRafWT), and 1.65 nM (CRaf), respectively
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DCC3991 panomifene
Tamoxifen analogue; antiestrogenic
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DCC3990 Panduratin A
Biological Active Reagents
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DCC3989 Pancratistatin
Inhibitor of the Cell_cycle>cell cycle from G0/G1 to S phase with powerful antiparasite activity
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DCC3988 Pam2cys
Novel TLR2 agonist as potential adjuvant for cancer vaccines
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DCC3987 Palonosetron
Potent serotonin-3 (5-HT3) receptor antagonist
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DCC3986 Palmostatin M
Novel Ras-Signaling Modulator, targeting acyl protein thioesterase 1 (APT1) and 2 (APT2) in cells
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DCC3984 Pal-545 Hydrochloride
Potent dual dopamine-serotonin (DA/5-HT) releaser
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DCC3983 pal-287
Full DAT/5-HT transporter substrate; Non-neurotoxic releasing agent of serotonin, norepinephrine, and dopamine; Full agonist at 5-HT2B and partial agonist at 5-HT2C
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DCC3982 Pal-12
Novel selective LYPLAL1 activator, increasing LYPLAL1’s catalytic activity likely by enhancing the efficiency of the catalytic triad charge-relay system, confering beneficial effects in a mouse model of diet-induced obesity
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DCC3981 pal-1046
Full DAT/5-HT transporter substrate
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DCC3980 pal-1045
Partial DAT/5-HT transporter substrate
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DCC3979 Pad3-in-14b
Novel potent and selective inhibitor of protein arginine deiminase 3 (PAD3), having 15600 kinact/KI values and ≥10-fold selectivity for PAD3 over PADs 1, 2, and 4.
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DCC3978 Paba/no
Novel glutathione-S-transferase-p-activated nitric oxide donor, inhibiting proliferation and inducing apoptosis by targeting PI3K/AKT/mTOR and MEK/ERK pathways in hepatocellular carcinoma cells
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DCC3977 Pa1 Dihydrochloride
Photoswitchable epithelial sodium channel (ENaC) blocker
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DCC3976 Pa-082
Novel partial agonist of peroxisome proliferator-activated receptor-γ (PPARγ), recruiting PPARγ-coactivator-1α, preventing triglyceride accumulation, and potentiating insulin signaling in vitro
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DCC3975 Pa Autoinducer
Pseudomonas aeruginosa autoinducer
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DCC3974 P97-in-23
Novel potent inhibitor of the AAA+ ATPase p97
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DCC3973 P97-in-17
Novel potent inhibitor of the AAA+ ATPase p97
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DCC3972 P7c3a20
Neuroprotective agent, protecting ventral horn spinal cord motor neurons from cell death
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DCC3971 P7 Peptide
Novel bFGF antagonist peptide, inhibiting breast cancer cell growth
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DCC3970 P5-peptide
Novel inhibitor of atherogenesis and diabetes, significantly and specifically inhibiting αD-CEP binding
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