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  • Inhibitors & Agonists
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    TargetMol | Inhibitors_Agonists
tak-615
T96991664335-55-0
TAK-615 is commonly used to study pulmonary fibrosis and is a negative allosteric modulator of LPA1 receptors.
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SP 600125, negative control
JNK Inhibitor II, negative control
T3826054642-23-8
SP 600125, negative control is a methylated analog of SP 600125 and can be used as a negative control for SP 600125. SP 600125, negative control inhibits DTP3 and GADD45β MKK7 (growth arrest and DNA damage-inducible β mediator-activated protein kinase kinase kinase 7) and is capable of restoring activation.The IC50s of SP 600125, negative control against JNK2 and JNK3 were 18 and 24 μM, respectively.
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TargetMol | Inhibitor Sale
ELA-14 negative control
T393171885873-44-8
ELA-14 negative control is an inactive peptide that serves as a negative control for ELA-14.
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ARCC 4 negative control
T412272156588-26-8
ARCC 4 negative control is a negative control for ARCC 4. Binds androgen receptors (AR) without inducing degradation.
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ERK Inhibitor II (Negative control)
T713161177970-73-8
ERK Inhibitor II (Negative control) effectively blocks extracellular signal-regulated kinase (ERK) activity and interferes with insulin receptor activation, serving as a valuable tool in diabetes research.
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8-10 weeks
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Anti gram-positive/negative bacteria agent 1
T73997
Anti gram-positive negative bacteria agent 1 is an antibiotic conjugated with a synthetic MECAM-based siderophore, designed to combat both gram-positive and gram-negative bacteria.
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SiRNA Negative Control
T74869
SiRNA Negative Control is an siRNA sequence that does not target any gene product and is a negative control for siRNA.
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7-10 days
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Bax inhibitor peptide, negative control
TP22031315378-74-5
The compound is a negative control peptide for the Bax inhibitor peptides V5 and P5.
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Ampicillin
D-(-)-α-Aminobenzylpenicillin, Ampicillin acid, Aminobenzylpenicillin, Amcill
T0814L69-53-4
Ampicillin (Aminobenzylpenicillin) is a semi-synthetic penicillin belonging to the β-lactam group of antibiotics. Ampicillin has bactericidal activity against a wide range of Gram-positive and Gram-negative bacteria.
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TargetMol | Inhibitor Hot
Lipopolysaccharides
LPS
T11855
Lipopolysaccharides (LPS) derived from Escherichia coli 055:B5, are a unique component of the cell wall of Gram-negative bacteria. They are composed of three regions: lipid A, oligosaccharide core, and O-specific polysaccharide (O-antigen). Lipopolysaccharides help maintain the integrity of the cell outer membrane and protect bacteria from damage by bile salts and lipid antibiotics. Lipopolysaccharides are highly immunogenic antigens that can enhance immune responses and can be used to construct inflammatory models.
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TargetMol | Inhibitor Hot
Nitrocefin
T1970941906-86-9
Nitrocefin is an antibiotic. It being sensitive to hydrolysis by all lactamases produced by gram-positive and gram-negative bacteria.
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TargetMol | Inhibitor Hot
Datopotamab deruxtecan
S-1062a, DS-1062, DS1062, Dato-DXd
T397302238831-60-0
Datopotamab deruxtecan (DS-1062) is a trophoblast cell surface antigen 2 (TROP2)-targeted antibody-drug conjugate (ADC) with antitumor activity. Datopotamab deruxtecan induces significant antibody-dependent cellular cytotoxicity in the presence of peripheral blood lymphocytes and inhibits tumor growth in xenograft models.
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2-4 weeks
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TargetMol | Inhibitor Hot
Zavondemstat
TACH 101 free base, QC8222 free base
T701211851412-93-5In house
Zavondemstat (QC8222 free base) is a histone lysine demethylase 4 (KDM4) inhibitor with anticancer and antitumor activity for the study of triple-negative and breast cancers.
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7-10 days
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TargetMol | Inhibitor Hot
CDK4/6/1 Inhibitor
Crozbaciclib
T107352099128-41-1In house
CDK4 6 1 Inhibitor (Crozbaciclib) is a type of CDK4 6 inhibitor (IC50s: 3 and 1 nM). CDK4 6 inhibitor is a class of compounds used for the treatment of some types of hormone receptor positive, HER2-negative breast cancer, which can block the process of breast cancer cell division and reproduction.
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6-8weeks
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Dopamine D2 receptor antagonist-1
T110771055411-77-2In house
Dopamine D2 Receptor Antagonist-1 functions as a negative allosteric modulator (NAM) of the dopamine D2 receptor (D2R), demonstrating sub-millimolar affinity.
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6-8 weeks
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(E)-GABAB receptor antagonist 1
T111371611483-29-4In house
(E)-GABAB receptor antagonist 1 is a trans-GABAB receptor antagonist that decreases GABA-induced IP3 (inositol trisphosphate) production with an IC50 of 37.9 μM. It is a selective and negative allosteric modulator of GABAB (γ-Aminobutyric acid) receptors.
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6-8 weeks
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TargetMol | Inhibitor Sale
GNE-1858
T114382680616-96-8In house
GNE-1858 is an ATP-competitive hematopoietic progenitor kinase-1 (HPK1) inhibitor (IC50s of 1.9 nM, 1.9 nM, and 4.5 nM for wild-type and the active mimetic mutants HPK1-TSEE and HPK1-SA).
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6-8 weeks
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PNU288034
T12512383199-88-0In house
PNU288034, a potent oxazolidinone antibiotic, demonstrates antimicrobial activity for the prevention and treatment of Gram-negative infections.
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6-8 weeks
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Sapienic acid sodium
T12830217477-25-3In house
Sapienic acid sodium is a fatty acid with variable antimicrobial activities against Gram-positive and Gram-negative bacteria found on the skin and in the oral cavity.
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6-8 weeks
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VU6012962
T133232313526-86-0In house
VU6012962 is an orally bioavailable negative allosteric modulator of CNS-penetrant metabotropic glutamate receptor 7(mGlu7; IC50: 347 nM).
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6-8 weeks
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Tigemonam
T13926102507-71-1In house
Tigemonam is a monobactam, a novel orally administered monobactam that protects against gram-negative aerobic bacterial pathogens and is at least as active against clinical isolates of Enterobacteriaceae as amitraz or carmonan (MIC90: 0.06-16 mg l). [3]
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10-14 weeks
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TargetMol | Inhibitor Sale
0990CL
T13983511514-03-7In house
0990CL is an effective heterotrimer Gαi subunit specific inhibitor, which can interact with purified Go± in GDP-bound state, and can block α2AR mediated cAMP regulation. In the cell model, low concentration of 0990CL could partially restore cAMP level, and high concentration of 0990CL (10μM) began to have negative effects on cell viability.
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8-10 weeks
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AZ10606120 dihydrochloride
T14366607378-18-7In house
AZ10606120 dihydrochloride is a selectable, potent, high-affinity receptor antagonist with K D values of 1.4 and 19 nM at human and rat P2X 7 receptors, respectively. AZ10606120 dihydrochloride inhibits tumor growth and has anti-angiogenic activity. AZ 10606120 acts as a negative allosteric modulator when bound to a site coupled to the ATP binding site.
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6-8 weeks
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Centrinone-B
LCR-323, LCR 323, LCR323
T149261798871-31-4In house
Centrinone-B (LCR-323) is a potent and highly selective PLK4 inhibitor with a Ki of 0.59 nM.
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6-8 weeks
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