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Cat. No. Product Name Field of Application Chemical Structure
DC42578 (-)-ML206
Less active enantiomer of ML206 (AOB1395), acting as a modulator of lipid storage
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DC42575 HyT36(-Cl) (Deschloro-HyT36)
Control molecule for HyT36 (AOB4848) which is a hydrophobic inducer of the degradation of stabilized proteins
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DC42569 HJ-PI01
Novel Pim-2 inhibitor, inducing apoptosis and autophagic cell death in triple-negative human breast cancer
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DC42567 SC-10
PKC activator, stimulating PKC mediated myosin light chain phosphorylation without activating MLC kinase
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DC42566 Fluzinamide
Antiepileptic anticonvulsant, significantly attenuating after discharge durations and the severity of the accompanying convulsive responses
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DC42564 Pemafibrate sodium
Novel selective PPARalpha modulator (SPPARMalpha), improving dyslipidemia, enhancing reverse cholesterol transport and decreasing inflammation and atherosclerosis
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DC42563 Varespladib Sodium
Selective Phospholipase A2 Inhibitor
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DC42562 Autogramin-2
Novel autophagy inhibitor, selectively targeting cholesterol transfer protein GRAM domain-containing protein 1A (GRAMD1A), and directly competing with cholesterol binding to the GRAMD1A StART domain
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DC42565 PF-562271 HCl
Novel focal adhesion kinase (FAK) inhibitor
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DC43047 Thunberginol C
DC42547 [Tyr11]-Somatostatin
[Tyr11]-Somatostatin is a neuroavtive peptide for proteomics research. Somatostatin is one of many neuroactive substances that influence retinal physiology.
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DC42546 THK5351
THK5351 can be radiolabeled and used as a radiotracer for in vivo imaging of tau pathology in the brain.
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DC42545 Cytidine 5'-diphosphate trisodium salt
Cytidine 5'-diphosphate trisodium salt (CDP) is produced by the transfer of phosphoryl group from ATP to cytidine monophosphate (CMP) catalyzed by uridine monophosphate kinase (UMPK). Cytidine 5′-diphosphate can be used to produce Cytidine triphosphate (CTP) for synthesis of DNA and RNA.
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DC42544 FD-1080
FD-1080 is a fluorophore with both excitation and emission in the NIR-II region (Ex=1064 nm, Em=1080 nm). FD-1080 can be uesd in vivo imaging.
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DC42543 4-Hydroxy-1H-indole-3-carbaldehyde
4-Hydroxy-1H-indole-3-carbaldehyde is a plant metabolite that found in Capparis spinosa L.. 4-Hydroxy-1H-indole-3-carbaldehyde can be used in the synthesis of fluorescent probe.
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DC42542 PINT-87aa
PINT-87aa is an 87-amino acid (aa) peptide that directly interacts with polymerase associated factor complex (PAF1c) and inhibits the transcriptional elongation of multiple oncogenes. PINT-87aa suppresses glioblastoma cell proliferation in vitro and in vivo.
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DC42541 PINT-87aa TFA
PINT-87aa TFA is an 87-amino acid (aa) peptide that directly interacts with polymerase associated factor complex (PAF1c) and inhibits the transcriptional elongation of multiple oncogenes. PINT-87aa TFA suppresses glioblastoma cell proliferation in vitro and in vivo.
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DC42540 Sodium phenylpyruvate
Sodium phenylpyruvate (Phenylpyruvic acid sodium salt) inhibits amino acid formation and depresses oxygen consumption.
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DC42539 3,4,5-Trihydroxycinnamic acid decyl ester
3,4,5-Trihydroxycinnamic acid decyl ester is an excellent inhibitor of lipid absorption and accumulation, anti-obesity properties. 3,4,5-Trihydroxycinnamic acid decyl ester is a pancreatic lipase inhibitor, with an EC50 of approximately 0.9 μM.
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DC42538 2-Iodoacetamide
2-Iodoacetamide (Iodoacetamide), an alkylating agent, is a commonly used agent for alkylation of cysteine during sample preparation for proteomics.
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DC42536 653-47 hydrochloride
653-47 hydrochloride, a potentiator, significantly potentiates the cAMP-response element binding protein (CREB) inhibitory activity of 666-15. 653-47 hydrochloride is also a very weak CREB inhibitor with IC50 of 26.3 μM.
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DC42535 653-47
653-47, a potentiator, significantly potentiates the cAMP-response element binding protein (CREB) inhibitory activity of 666-15. 653-47 is also a very weak CREB inhibitor with IC50 of 26.3 μM.
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DC42534 KS15
KS15 is an inhibitor of the interactions between cryptochromes (CRYs: CRY1 and CRY2) and the CLOCK:BMAL1 heterodimer. KS15 impairs the feedback actions of CRYs on E-box-dependent transcription (EC50=4.9 μM) by CLOCK:BMAL1 heterodimer, an indispensable transcriptional regulator of the mammalian circadian clock. Anti-proliferative activity.
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DC42533 8-Hydroxycoumarin
8-Hydroxycoumarin is an intermediate in the microbial transformation of quinolone.
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DC42532 Fullerene-C60
Fullerene-C60, a representative of carbon nanocompounds, is suggested to be promising agent for application in photodynamic therapy due to its unique physicochemical properties. Fullerene-C60 probes the intramolecular dynamics of its electron and energy transfer.
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DC42529 4-Hydroxyindole
4-Hydroxyindole is a member of the class of hydroxyindoles that is 1H-indole substituted by a hydroxy group at position 4. 4-Hydroxyindole is an important raw material or intermediate in the synthesis of pharmaceutical products and industrial polymers.
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DC42528 Fmoc-D-Trp(Boc)-OH
Fmoc-D-Trp(Boc)-OH is a cleavable ADC linker that used in the synthesis of antibody-drug conjugates (ADCs).
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DC42527 Sucrose-epichlorohydrin copolymer
Sucrose-epichlorohydrin copolymer acts as a macromolecular crowder and promotes protein liquid-liquid phase separation (LLPS) .
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DC21610 Tafenoquine succinate Featured
Tafenoquine succinate (SB-252263, Tafenoquine, WR 238605) is a long-acting, orally active anti-malarial agent to prevent malaria that is holoendemic for Plasmodium falciparum..
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DC10064 GSK-F1 Featured
GSK-F1 is a potent inhibitor of PI4KA.
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