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Results for "

lactam

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    172
    TargetMol | Inhibitors_Agonists
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    2
    TargetMol | Compound_Libraries
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    5
    TargetMol | Peptide_Products
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D-Lysine lactam
T3605328957-33-7
D-Lysine lactam is a chiral building block.1,2It has been used in the synthesis of a chiral antibiotic synthetic intermediate, as well as in the stereoselective synthesis of neurokinin (NK) receptor antagonists. 1.Kumar, A., Bhashkar, B., Bhavsar, J., et al.Catalytic reduction: Efficient synthesis of chiral key intermediate of besifloxacin hydrochlorideDer Pharma Chemica7(9)297-3000(2015) 2.Gerspacher, M., Lewis, C., Ball, H.A., et al.Stereoselective preparation of N-[(R,R)-(E)-1-(3,4-dichlorobenzyl)-3- (2-oxoazepan-3-yl)carbamoyl]allyl-N-methyl-3,5-bis(trifluoromethyl)benzamide, a potent and orally active dual neurokinin NK(1)/NK(2) receptor antagonistJ. Med. Chem.46(16)3508-3513(2003)
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L-Lysine lactam (hydrochloride)
T3642226081-07-2
L-lysine lactam is a building block.1,2It has been used in the synthesis of lysine sulfonamide HIV protease inhibitors, as well as bengamide derivatives within vitroanticancer activity.
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Olanzapine Lactam Impurity
T377041017241-34-7
Olanzapine lactam impurity is a potential impurity found in commercial preparations of olanzapine.1It is a degradation product formed by exposure to thermal or oxidative stress. 1.Baertschi, S.W., Brunner, H., Bunnell, C.A., et al.Isolation, identification, and synthesis of two oxidative degradation products of olanzapine (LY170053) in solid oral formulationsJ. Pharm. Sci.97(2)883-892(2008)
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D-Ornithine lactam
T6846288763-76-2
D-Ornithine lactam is a building block. It has been used in the synthesis of hepatitis C virus non-structural protein 5B inhibitors, as well as αVβ3 integrin receptor antagonists.
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6-8 weeks
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L-Ornithine lactam hydrochloride
T7183142538-31-8
L-Ornithine lactam is a synthetic intermediate. It has been used in the synthesis of dipeptidyl peptidase 4 (DPP-4) inhibitors, as well as signaling peptides.
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6-8 weeks
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N-Methyl lactam
T87025116212-46-5
N-Methyl lactam (Compound 3b), an analogue of peramiue, exhibits feeding-deterrent activity in adult weevils [1].
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10-14 weeks
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Caprolactam
T20386105-60-2
Caprolactam is a natural product used in the manufacture of synthetic fibers of the polyamide type.
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4-6 weeks
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β-Lactamase-IN-2
T354272114651-20-4
β-Lactamase-IN-2 is an inhibitor of β-Lactamase with anti-microbial and anti-bacterial effects.
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6-8 weeks
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TargetMol | Inhibitor Sale
Metallo β-lactamase ligand 1
T384761087784-71-1
Metallo β-lactamase ligand 1 is an inhibitor of class B β-lactamase exhibiting antibacterial activities.
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TargetMol | Inhibitor Sale
Metallo-β-lactamase-IN-3
T60282128294-71-3
Metallo-β-lactamase-IN-3 (compound 35) is a potent metallo-β-lactamases (MBL) inhibitor that can potentially restore the activity of current β-lactam antibiotics and provide an orthogonal strategy for discovering new antibiotics. It exhibits high activity against VIM-1 and NDM-1, with IC50 values of 0.6 and 1.0 μM, respectively, but does not inhibit IMP-7 [1].
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6-8 weeks
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Aristololactam II
T124662
Aristololactam II is a useful organic compound for research related to life sciences and the catalog number is T124662.
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Stigmalactam
T125112
Stigmalactam is a useful organic compound for research related to life sciences and the catalog number is T125112.
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Spirodihydrobenzofuranlactam IV
T125587173220-03-6
Spirodihydrobenzofuranlactam IV is a useful organic compound for research related to life sciences. The catalog number is T125587 and the CAS number is 173220-03-6.
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Aburatubolactam A
T125605
Aburatubolactam A is a useful organic compound for research related to life sciences and the catalog number is T125605.
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Piperolactam D
T126315116084-93-6
Piperolactam D is a useful organic compound for research related to life sciences. The catalog number is T126315 and the CAS number is 116084-93-6.
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Sauristolactam
Saurolactam
T16846128533-02-8
Sauristolactam inhibits the receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclastogenesis and has the potential to inhibit osteoclast differentiation. Sauristolactam, a natural aristolactam isolated from aerial portions of Saururus Chi
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(-)-Indolactam V
Indolactam V
T1729990365-57-4
(-)-Indolactam V, a potent PKC activator, exhibits binding affinities (Kis) of 3.36 nM and 1.03 μM for η-CRD2 and γ-CRD2, respectively, and dissociation constants (Kds) of 5.5 nM (η-C1B), 7.7 nM (ε-C1B), 8.3 nM (δ-C1B), 18.9 nM (β-C1A-long), 20.8 nM (α-C1A-long), 137 nM (β-C1B), 138 nM (γ-C1A), and 213 nM (γ-C1B), also demonstrating antitumor activity.
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8-10 weeks
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β-Lactamase-IN-1
beta-lactamase-IN-1, 4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one
T192061075237-97-6
β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) is a β-Lactamase inhibitor and targets the infection of Neisseria gonorrhoeae.
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6-8 weeks
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Metallo-β-lactamase-IN-16
T2010212058069-25-1
Metallo-β-lactamase-IN-16 (compound 18), a sulfone-containing metallo-β-lactamase inhibitor, exhibits antimicrobial activity. It effectively inhibits various metallo-β-lactamases, including NDM-1 (New Delhi metallo-β-lactamase-1), IMP-1 (imipenemase-1), VIM-1 (Verona Integron-encoded Metallo-β-lactamase), and VIM-2. The IC50 values for these enzymes are 0.16 nM, 0.23 nM, 0.31 nM, and 1.0 nM respectively.
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3-6 months
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Atrolactamide
T251172019-68-3
Atrolactamide is an anticonvulsant.
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6-8 weeks
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β-Lactamase-IN-4
T389551463520-91-3
β-Lactamase-IN-4 (WO2013149121A1, compound 708) is a potent β-lactamase inhibitor. It serves as a valuable tool in the investigation of bacterial infections.
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β-Lactamase-IN-5
T389561463521-39-2
β-Lactamase-IN-5, a β-lactamase inhibitor isolated from compound 720, holds significant potential for studying bacterial infections.
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β-Lactamase-IN-6
T398652326468-84-0
β-Lactamase-IN-6 is a β-lactamase inhibitor with high antibacterial activity.
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Aristolactam I
Aristolactam, Aristololactum, Aristololactam I
T3S122713395-02-3
1.Aristolactam I (Aristololactum) has cytotoxic potency, mediated through the induction of apoptosis in a caspase 3-dependent pathway. 2. The effects of Aristololactam I may be mediated by different mechanisms except TGF-beta1 pathway. 3. Aristololactam I may be one of toxic metabolites in Chinese herbs containing AA which participate in renal damage and fibrosis.
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