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Cat. No. Product Name Field of Application Chemical Structure
DC47444 Carboxylesterase-IN-1
Carboxylesterase-IN-1, a novel pesticide, exhibits inhibitory action on carboxylesterase at 50 μg/mL similar to the known inhibitor triphenyl phosphate.
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DC47442 FTO-IN-3
FTO-IN-3 is a FTO inhibitor that impair self-renewal in glioblastoma stem cells.
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DC47441 FTO-IN-2
FTO-IN-2 is a FTO inhibitor that impairs self-renewal in glioblastoma stem cells.
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DC47440 BTNPO
BTNPO is a unimolecular two-photon fluorescent probe.
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DC47439 Cavα2δ-IN-1
Cavα2δ-IN-1 shows high selectivity for voltage-gated calcium channels Cavα2δ-1 (Ki 6 nM) versus Cavα2δ-2 (Ki > 10000 nM).
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DC47437 Br-DAPI
Br-DAPI is a water-soluble, cell-permeable, DNA-binding photosensitizer.
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DC47436 ARN19689
ARN19689 is found to inhibit human NAAA in the low nanomolar range (IC50 = 0.042 μM) with a non-covalent mechanism of action.
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DC47435 c-ABL-IN-1
c-ABL-IN-1 is a novel selective c-Abl inhibitor that prevents neurodegeneration in parkinson’s disease.
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DC47432 CXCL12 ligand 1
CXCL12 ligand 1 is the first ligand of the sY12-binding pocket on chemokine CXCL12.
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DC47430 HOPan
HoPan inhibits phosphopantotenoylcysteine synthetase activity.
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DC47429 HAV 3C proteinase-IN-1
HAV 3C proteinase-IN-1 is a inhibitor of Hepatitis A virus 3C proteinase.
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DC47426 GT-1
GT-1 (LCB10-0200), a siderophore-linked cephalosporin, is effective against clinical isolates of P. aeruginosa, Klebsiella oxytoca, Proteus spp., Serratia marcescens, and Enterobacter aerogenes.
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DC47424 CR-1-30-B
CR-1-30-B is an inactive enantiomer of CR-1-31-B. CR-1-30-B, as a control, is inactive against eIF4A and has no apparent effect on the induction of MUC1-C translation.
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DC47416 CYPMPO
CYPMPO is a spin-trapping reagent. CYPMPO, a cyclic DEPMPO-type nitrone, is evaluated for spin-trapping capabilities toward hydroxyl and superoxide radicals. anti-oxidant and anti-tumor activity.
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DC47330 BRD4 ligand-Linker Conjugate 1
BRD4 ligand-Linker Conjugate 1 is a target protein ligand-linker conjugate that can be used in the synthesis of PROTACs.
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DC47329 Ficusonolide
Ficusonolide has significant antidiabetic activity with a possible mechanism of interaction with dipeptidyl peptidase-IV (DPP-IV), protein tyrosine phosphatase 1B (PTP-1B), α-glucosidase, and α-amylase.
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DC47855 Anti-inflammatory agent 5
Anti-inflammatory agent 5 displays potent inhibition of NO generation in lipopolysaccharide-induced BV-2 microglial cells.
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DC47854 (3ξ,4ξ,5ξ,6ξ,7ξ,11ξ)-3,6-Dihydroxy-8-oxo-9-eremophilene-12-oic acid
(3ξ,4ξ,5ξ,6ξ,7ξ,11ξ)-3,6-Dihydroxy-8-oxo-9-eremophilene-12-oic acid is a new phytotoxin of Alternaria alternata ssp. tenuissima isolates associated with fruit spots on apple.
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DC47853 (9S)-Macrocidin B
(9S)-Macrocidin B shows a weaker herbicidal effect than macrocidin A.
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DC47852 Amakusamine
Amakusamine inhibits the receptor activator of nuclear factor-κB ligand (RANKL)-induced formation of multinuclear osteoclasts with an IC50 value of 10.5 μM in RAW264 cells.
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DC47846 14-Benzoylneoline
14-Benzoylneoline is found in Aconitum subcuneatum.
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DC47836 3,5-O-Dicaffeoylquinic acid
3,5-O-Dicaffeoylquinic acid reverses Trimethyltin-induced learning and memory deficits.
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DC47826 3β-Methoxy-2,3-dihydrowithaferin A
3β-Methoxy-2,3-dihydrowithaferin A is one of withanolides found in Withania somnifera.
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DC47824 2-Hydroxyanthraquinone
2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity.
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DC47817 (±)-Phrymarolin II
(±)-Phrymarolin II is a promising new class of plant virus (tobacco mosaic virus) inhibitors.
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DC47808 2,3-Didehydrosomnifericin
2,3-Didehydrosomnifericin is one of withanolides found in Withania somnifera.
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DC47803 7,22,25-Stigmastatrienol
7,22,25-Stigmastatrienol is one of sterols of Berrettina pumpkin seed oil.
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DC47796 2,3-Bis(3-indolylmethyl)indole
2,3-Bis(3-indolylmethyl)indole significantly suppresses RANKL-induced osteoclast formation, actin ring formation, and bone resorption in a concentration-dependent manner.
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DC47794 3'-Geranyl-3-prenyl-2',4',5,7-tetrahydroxyflavone
3'-Geranyl-3-prenyl-2',4',5,7-tetrahydroxyflavone displays cytotoxicity of 1.32, 3.92 and 5.22 μm against the human cervical carcinoma HeLa, human breast carcinoma MCF-7, and human hepatocarcinoma Hep3B cells.
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DC47792 25(S)-Ruscogenin-1-O-α-L-rhamnopyranosyl (1→2)-β-D-xylopyranoside
25(S)-Ruscogenin-1-O-α-L-rhamnopyranosyl (1→2)-β-D-xylopyranoside shows inhibitory activity of neutrophil respiratory burst stimulated by PMA(phorbol myristate acetate).
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