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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC48769 | Sterpurol D |
Sterpurol D is a compound of the sterpurane sesquiterpenoid. Sterpurol D significantly inhibits nitric oxide (NO) production.
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| DC48767 | Britannilactone diacetate |
Britannilactone diacetate shows potential antiinflammatory, antibacterial, antihepatitic, antidiabetes, and antitumor activities.
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| DC48764 | Tetrahydroauroglaucin |
Tetrahydroauroglaucin is a member of hydroquinones, with antioxidative effects.
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| DC48759 | TLR4/NF-κB/MAPK-IN-1 |
TLR4/NF-κB/MAPK-IN-1 is a new type of antineuroinflammatory agent by suppressing TLR4/NF-kB/MAPK pathways.
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| DC48754 | Clomipramine |
Clomipramine (Chlorimipramine) is a potent 5-HT reuptake blocker with the IC50 value of 1.5 nM. Clomipramine is a tricyclic antidepressant that can be used for the research of depression and obsessive compulsive disorder (OCD).
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| DC48752 | KF38789 |
KF38789 is a selective inhibitor of P-selectin-PSGL-1 binding. KF38789 inhibits the binding of U937 cells to immobilized P-selectin immunoglobulin G chimeric protein (P-selectin-Ig) with an IC50 value of 1.97 μM.
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| DC48739 | 5-Ph-IAA-AM |
5-Ph-IAA-AM is an eggshell-permeable 5-Ph-IAA analog. 5-Ph-IAA-AM affords an enhanced protein degradation in laid embryos. 5-Ph-IAA-AM can be used to disclosure the roles of proteins in C. elegans, in particular those that are involved in embryogenesis and development, through temporally controlled protein degradation.
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| DC48734 | Difenpiramide |
Difenpiramide (Z-876) is a bisphenylalcanoic derivative with marked anti-inflammatory, analgesic, antipyretic and uricosuric properties. Difenpiramide has platelet anti-aggregation activity.
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| DC48731 | Phenol Red |
Phenol red (Phenolsulfonephthalein) is a pH indicator dye, relying on a distinct color change from pink to yellow in case of a positive reaction .
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| DC48726 | GEM–IB |
GEM–IB is the conjugate of gemcitabine (GEM)-5'-phosphate with ibandronate (IB). GEM–IB as a single agent or in combination with Docetaxel (DTX) demonstrates reduced tumor burden, preservation of the bone architecture, and improved the survival in a murine model of osteosarcoma (OS).
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| DC48725 | PptT-IN-1 |
PptT-IN-1 (compound 5j) is a potent inhibitor of with phosphopantetheinyl phosphoryl transferase (PptT) an IC50 of 2.8 μM. Phosphopantetheinyl transferase, an essential enzyme that plays a critical role in the biosynthesis of cellular lipids and virulence factors in Mycobacterium tuberculosis. PptT-IN-1 has the potential for the research of tuberculosis.
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| DC48720 | Integerrimine N-oxide |
Integerrimine N-oxide, the main pyrrolizidine alkaloid found in the butanolic residue (BR) of Senecio brasiliensis. Prenatal exposure to integerrimine N-oxide induces maternal toxicity, impairment of maternal care and delays in physical and behavioral development of the offspring.
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| DC48713 | Myt1-IN-3 |
Myt1-IN-3 is a potent Myt1 inhibitor with an IC50s of <10 nM (WO2021195782 A1, compound 95).
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| DC48711 | RXFP3 agonist 1 |
RXFP3 agonist 1 is a nonpeptide RXFP3 agonist (EC50=6937 nM).
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| DC48707 | Myt1-IN-2 |
Myt1-IN-2 is a potent Myt1 inhibitor with an IC50 of <10 nM. Myt1-IN-2 has anticancer effects (WO2021195782A1; compound 28).
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| DC48705 | TTBK1-IN-2 |
TTBK1-IN-2 (compound 29) is a potent Tau-Tubulin kinase (TTBK1) inhibitor with IC50s of 0.24 and 4.22 µM, respectively. TTBK1-IN-2 reveals good brain penetration in vivo and is able to reduce TDP-43 phosphorylation not only in cell cultures but also in the spinal cord of transgenic TDP-43 mice.
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| DC48704 | Antitumor agent-31 |
Antitumor agent-31 is a nanosized chelates of anchoring bisazo dye. Antitumor agent-31 can be used for an antioxidant and antitumor agent.
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| DC48702 | RBM10-8 |
RBM10-8 irreversibly inhibits human sphingosine-1- phosphate lyase (hS1PL) while behaving also as an enzyme substrate.
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| DC48697 | Lascivol |
Lascivol is a bitter compound isolated from Tricholoma species.
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| DC48695 | α-Obscurine |
α-Obscurine is a lycodine-type alkaloid.
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| DC48687 | 9-Demethyl FR-901235 |
9-Demethyl FR-901235 is the 9-demethyl derivative of immunomodulator FR-901235.
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| DC48686 | photoCORM-2 |
photoCORM-2 (compound 3) is a single carbon monoxide releasing molecule (CORM). photoCORM-2 exhibits good cellular uptake and real-time monitoring ability of CO uncaging by a color change approach. photoCORM-2 has anti-tumor activity.
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| DC48685 | Lonazolac |
Lonazolac is a non-steroidal antirheumatic agent. Anti-inflammatory effects .
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| DC48676 | 2-Hexyldecanoic acid |
2-hexyldecanoic acid can be used as an amidating agent .
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| DC48674 | Thymotrinan |
Thymotrinan (RGH-0205) is a biologically active fragment of the naturally occurring thymus hormone thymopoietin and a immunomodulating peptide. Thymotrinan exerts similar immunomodulatory activities to TP5 and to affect humoral as well as cellular responses.
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| DC48672 | BIOTIN-PEG11-SH |
BIOTIN-PEG11-SH enables biotin labeling of protein.
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| DC48669 | PptT-IN-3 |
PptT-IN-3 (compound 5p) is a potent inhibitor of with phosphopantetheinyl phosphoryl transferase (PptT) an IC50 of 3.5 μM. Phosphopantetheinyl transferase, an essential enzyme that plays a critical role in the biosynthesis of cellular lipids and virulence factors in Mycobacterium tuberculosis. PptT-IN-3 has the potential for the research of tuberculosis.
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| DC48668 | 6-(3,4,5-Trimethoxybenzamido)hexanoic acid |
6-(3,4,5-Trimethoxybenzamido)hexanoic acid is an antiarrythmic agent.
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| DC48666 | Biotin-4-aminophenol |
Biotin-4-aminophenol is a biotin-phenol analog. Biotin-4-aminophenol generates free radicals and conjugates to tyrosine residues in proteins more efficiently and selectively than the previously reported BP1.
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| DC48663 | Talaroenamine F |
Talaroenamine F is active against Bacillus cereus with an MIC value of 0.85 μg/mL.
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