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phenol, 3methyl, sodium salt (1:1)

" in TargetMol Product Catalog
  • Inhibitor Products
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Durlobactam sodium salt
T111251467157-21-6
Durlobactam sodium salt (ETX2514 sodium salt) is an inhibitor of β-lactamase with IC50 values of 4 nM, 14 nM, and 190 nM for Class A KPC-2, Class C AmpC, and Class D OXA-24, respectively. Durlobactam sodium salt can be used in studies about drug-resistant Gram-negative bacteria including Acinetobacter baumannii.
  • $390
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Aldose reductase-IN-1
T141751355612-71-3
Aldose reductase-IN-1 (AT-001) is a aldose reductase inhibitor (IC50: 28.9 pM).
  • $70
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Nigericin sodium salt
T309228643-80-3
Nigericin sodium salt is an antibiotic, an NLRP3 activator, and a cationic ion carrier. Nigericin sodium triggers the activation of the NALP3 inflammasome, which inhibits Golgi function and suppresses the growth of Gram-positive bacteria.
  • $31
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TargetMol | Citations Cited
PD-1/PD-L1-IN-10
T96162487550-41-2
PD-1/PD-L1-IN-10 is an orally active PD-1/PD-L1 inhibitor (IC50 of 2.7 nM) with potent anticancer efficacy.
  • $44
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(+)-JQ-1
T21101268524-70-4
(+)-JQ-1 (JQ1) is a BET bromine domain inhibitor that inhibits BRD4 (1/2) (IC50=77/33 nM) with specificity and reversibility. (+)-JQ-1 induces cell autophagy and inhibits cell proliferation.
  • $30
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1-Palmitoyl-sn-glycero-3-phosphocholine
T871217364-16-8
1-Palmitoyl-sn-glycero-3-phosphocholine (1-Hexadecanoyl-sn-glycero-3-phosphocholine) is a phosphocholine for fluorescent probe design
  • $39
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Mdivi-1
T1907338967-87-6
Mdivi-1 (Mitochondrial division inhibitor 1) is a mitochondrial division inhibitor that inhibits DRP1 and Dynamin I (IC50=1-10 μM). Mdivi-1 inhibits mitochondrial autophagy.
  • $39
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TLR7/8-IN-1
T380782205095-75-4
TLR7/8-IN-1, a crystalline TLR7/TLR8 inhibitor, is a valuable compound for autoimmune disease research[1].
  • $189
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T3Inh-1
T972050440-30-7
T3Inh-1 is an effective and selective inhibitor of ppGalNAc-T3 with an IC50 of 7 µM. T3Inh-1 prevents breast cancer cells. T3Inh-1 reduces FGF23 hormone levels in both tissue cells and mice, without causing any toxic side effects.
  • $115
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SETDB1-TTD-IN-1
T97422755823-12-0In house
SETDB1-TTD-IN-1 is a potent, selective and endogenous binder competitive inhibitor of SETDB1-TTD with a Kd of 88 nM.
  • $269
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TargetMol | Citations Cited
CD38 inhibitor 1
T149131700637-55-3
CD38 inhibitor 1 is an inhibitor of CD38. For hCD38 and mouse CD38, the IC50s are 7.3 nM and 1.9 nM.
  • $51
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OSMI-1
T164091681056-61-0In house
OSMI-1 is an O-GlcNAc transferase (OGT) inhibitor (IC50=2.7 μM) that is orally active and cell-permeable. OSMI-1 inhibits protein O-GlcNA acetylation without qualitatively altering cell-surface N- or O- linked glycans.
  • $34
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SIRT1-IN-1
T9648352554-02-0In house
SIRT1-IN-1 is a selective inhibitor of SIRT1 with an IC50 of 205 nM. SIRT1-IN-1 is an inhibitor of cytomegalovirus (CMV) with antiviral activity.
  • $97
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Liproxstatin-1
T2376950455-15-9
Liproxstatin-1 is a potent and selective inhibitor of ferroptosis (IC50=22 nM). Liproxstatin-1 protects cells from ferroptosis induced by ferroptosis inducers (e.g., Erastin, RSL3).
  • $48
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Necrostatin-1
T18474311-88-0
Necrostatin-1 (Nec-1) is a necrotic apoptosis inhibitor and RIP1 inhibitor with specificity. Necrostatin-1 inhibits TNF-α-induced necrotic apoptosis. Necrostatin-1 also inhibits IDO.
  • $30
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diABZI STING agonist-1 (Tautomerism)
T110352138498-18-5
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
  • $168
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2',3'-cGAMP sodium
T10065L2734858-36-5
2',3'-cGAMP sodium (2'-3'-cyclic GMP-AMP sodium) is a second messenger in cellular innate immunity and is catalyzed by cGAMP synthase (cGAS) under DNA binding conditions. 2',3'-cGAMP sodium binds to STING to form a dimer, inducing the production and expression of interferon-β and other cytokines.
  • $298
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DCLK1-IN-1
T84182222635-15-4
DCLK1-IN-1 is a selective and in vivo-compatible chemical probe of the DCLK1 kinase domain .
  • $107
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2-Hydroxy-1-methoxyanthraquinone
TN12096170-06-5
2-Hydroxy-1-methoxyanthraquinone (Alizarin 1-methyl ether) is a natural product isolated from Morinda lucida Benth. (Rubiaceae) with antibacterial activity.
  • $152
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GLP-1(7-36), amide
T3984107444-51-9
GLP-1(7-36), amide (MKC 253) is a peptide hormone released from intestinal L-cells upon nutrient consumption. It binds the GLP-1 receptor in the pancreas and displays various antidiabetic effects by potentiating glucose-induced secretion of insulin from pancreatic β-cells, increasing insulin expression.
  • $185
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Etomoxir sodium salt
T4535828934-41-4
Etomoxir sodium salt ((R)-Etomoxir sodium salt) is a carnitine palmitoyltransferase 1a (CPT-1a) inhibitor that blocks fatty acid synthesis. Etomoxir sodium salt has antitumor activity.
  • $55
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Pam3CSK4 TFA (112208-00-1 free base)
TP1067112208-01-2
Pam3CSK4 TFA (Pam3Cys-Ser-(Lys)4 TFA) is an agonist of toll-like receptor 1/2 (TLR1/2) (EC50 of 0.47 ng/mL for human TLR1/2).
  • $128
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TargetMol | Inhibitor Hot
Ferrostatin-1
T6500347174-05-4
Ferrostatin-1 (Fer-1) is a potent and selective inhibitor of ferroptosis. Ferrostatin-1 potently inhibits Erastin-induced ferroptosis in HT-1080 cells with an EC50 of 60 nM. Ferrostatin-1 also exhibits antioxidant and antifungal activities.
  • $59
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TargetMol | Citations Cited
1-Methylimidazole
T0575616-47-7
1-Methylimidazole is a metabolite of 1-methyl-2-thioimidazole (methimazole) which inhibits bone resorption.
  • $50
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3-Diethylamino-1-propanol
T40709622-93-5
3-Diethylamino-1-propanol exhibits anticonvulsant effects.
  • $41
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Dolutegravir intermediate-1
T110741335210-23-5
Dolutegravir intermediate-1 (1-(2,2-dimethoxyethyl)-5-methoxy-6-(methoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid) is a new synthetic Dolutegravir intermediate. Dolutegravir is an integrase inhibitor developed for the treatment of human immunodeficiency virus (HIV)-1 infection.
  • $42
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Trans-​2-​butene-​1,​4-​dicarboxylic acid
T52464436-74-2
Trans-2-butene-1,4-dicarboxylic acid (3-Hexenedioic Acid) is a normal human unsaturated dicarboxylic acid metabolite with increased excretion in patients with Dicarboxylic aciduria caused by fatty acid metabolism disorders The urinary excretion of Trans-2-butene-1,4-dicarboxylic acid is increased in conditions of augmented mobilization of fatty acids or inhibited fatty acid oxidation.
  • $30
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Potassium 7-hydroxy-1-naphthalenesulfona
TN705030252-40-5
Potassium 7-hydroxy-1-naphthalenesulfona (2-Naphthol-8-sulfonic Acid Potassium Salt) is naturally present in the fruit of the Rubiaceae gardenia, the flowers of the Iridaceae crocus, and the flowers and leaves of the Scrophulariaceae Scrophulariaceae.
  • $50
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1-Indanone
T056483-33-0
1-Indanone (Indan-1-one) is the intermediate od Indinavir.
  • $29
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1-Hexadecanol
T635936653-82-4
1-Hexadecanol (Hexadecan-1-ol), a fatty alcoholis, is utilized for making other chemicals.
  • $31
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7-Methoxy-1-tetralone
Fr122756836-19-7
7-Methoxy-1-tetralone may have insecticidal activity.
  • $50
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1-Dodecanol
T9514112-53-8
1-Dodecanol is an endogenous metabolite and a saturated fatty alcohol from coconut oil fatty acids. It has a floral odor and is used in detergents, Lepidopteran pheromone/sex attractant, lubricating oils, pesticides and pharmaceuticals.
  • $30
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Methyl indole-3-carboxylate
T5868942-24-5
Methyl indole-3-carboxylate (Methyl 3-indolecarboxylate) is a natural product isolated from Heracleum candicans.
  • $42
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Y1 receptor antagonist 1
T12155221697-09-2In house
Y1 receptor antagonist 1 (H 409-22 isomer) is the active isomer of H-409/22, a neuropeptide Y (NPY) Y1 receptor antagonist that dose-dependently antagonizes the vascular response to exogenous and endogenous NPY in pigs. lagodeoxycholic acid (H 409-22 isomer) is the active isomer of H-409/22, an antagonist of neuropeptide Y (NPY) Y1 receptor.
  • $353
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L-Threonine derivative-1
T13751852055-88-0In house
L-Threonine derivative-1 is acetylsalicylic acid-L-threonine ester with potential analgesic activity.
  • $293
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Valproic acid sodium salt
T16021069-66-5
Valproic acid sodium salt (Sodium Valproate) is the sodium salt form of valproic acid with anti-epileptic activity. Valproic acid sodium salt is converted into its active form, valproate ion, in blood. Although the mechanism of action remains to be elucidated, Valproic acid sodium salt increases concentrations of gamma-aminobutyric acid (GABA) in the brain, probably due to inhibition of the enzymes responsible for the catabolism of GABA. This potentiates the synaptic actions of GABA. Valproic acid sodium salt may also affect potassium channels, thereby creating a direct membrane-stabilizing effect.
  • $42
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TargetMol | Citations Cited
CK2/ERK8-IN-1
T108271085822-09-8In house
CK2/ERK8-IN-1 (TMCB) is a dual inhibitor of casein kinase 2 (CK2) (Ki: 0.25 µM) and ERK8 (IC50s: 0.50 μM) with pro-apoptotic efficacy. CK2/ERK8-IN-1 also binds to PIM1, DYRK1A, and HIPK2 (Kis: 8.65 µM, 11.9 µM, and 15.25 µM).
  • $30
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1-Benzyl-4-hydroxypiperidine
Fr127294727-72-4
Compound Fr12729 is a useful organic compound for research related to life sciences. The catalog number is Fr12729 and the CAS number is 4727-72-4.
    7-10 days
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    1-Methylpyrrolidine
    T8029120-94-5
    1-Methylpyrrolidine is extensively used in the synthesis of pyrrolidine based ionic liquids.
    • $30
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    Colistin methanesulfonate sodium salt
    T215188068-28-8
    Colistin methanesulfonate sodium salt (Colistimethate Sodium) is a cyclic polypeptide antibiotic from Bacillus colistinus, composed of Polymyxins E1 and E2.
    • $41
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    CB2 modulator 1
    T10696666261-80-9In house
    CB2 modulator 1 is a potent CB2 modulator. It can be used for the research for immune disorders, osteoporosis, inflammation, renal ischemia.
    • $30
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    8-Amino-1-Naphthalenesulfonic Acid
    T797182-75-7
    8-Amino-1-Naphthalenesulfonic Acid is a naphthalene derivative used as a fluorescent dye and as a reagent in organic synthesis. It is a highly fluorescent compound with a high Stokes shift, making it an ideal fluorescent marker for a wide range of biological systems.
    • $50
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    Deoxycholic acid sodium salt
    T5077302-95-4
    Deoxycholic acid sodium salt (Sodium deoxycholate) can activate the G protein-coupled bile acid receptor TGR5 that stimulates brown adipose tissue (BAT) thermogenic activity.
    • $38
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    1-Eicosanol
    TN6760629-96-9
    1-Eicosanol is a natural product isolated from Hypericum carinatum. 1-Eicosanol has antioxidant activity.
    • $42
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    1-IODOADAMANTANE
    T7034768-93-4
    1-IODOADAMANTANE (1-Adamantyl Iodide) is employed in the free-radical carbonylation reactions with alkenes.
    • $80
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    Monensin sodium salt
    T103322373-78-0
    Monensin sodium is an antiprotozoal agent produced by Streptomyces cinnamonensis.Monensin sodium salt (Monensin A sodium salt) causes a marked enlargement of the MVBs and regulates exosome secretion
    • $30
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    Genipin 1-β-D-gentiobioside
    T4S229929307-60-6
    Genipin 1-β-D-gentiobioside is a natural product for research related to life sciences. The catalog number is T4S2299 and the CAS number is 29307-60-6.
    • $100
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    3-Aminopropionitrile fumarate (2:1)
    T27692079-89-2
    3-Aminopropionitrile fumarate (2:1) (β-Aminopropionitrile fumarate) is an organic compound and antirheumatic agent used in veterinary medicine.
    • $39
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    4-Nitroquinoline 1-oxide
    T3536656-57-5
    4-Nitroquinoline 1-oxide (4-NQO) is a chemical carcinogen that induces mutations in bacteria, fungi, and animals through the formation of large amounts of purine adducts.
    • $42
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    Penicillin G sodium salt
    T095869-57-8
    Penicillin G sodium(Benzylpenicillin sodium) salt is a penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.
    • $47
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