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Results for "

ao

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    1066
    TargetMol | All_Pathways
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    2
    TargetMol | Compound_Libraries
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    73
    TargetMol | Peptide_Products
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    TargetMol | All_Dye_Reagents
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    TargetMol | PROTAC
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    TargetMol | Recombinant_Protein
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    TargetMol | Antibody_Products
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    TargetMol | All_Pathways
Sporogen-AO 1
Sporogen AO-1
T3643888418-12-6
Sporogen-AO 1, a compound from the commensal fungus Penicillium sp. G1-a14, is an inhibitor of human inducible nitric oxide synthase expression with antimalarial activity and strong cytotoxicity.
  • $548
4-6 weeks
Size
QTY
5-Hydroxy-1-(4-hydroxyphenyl)-7-phenyl-3-heptanone (AO 2210)
TN3114105955-04-2
(±)-5-hydroxyl-1-(4'-hydroxyphenyl)-7-phenyl-3-heptanone have digestibility inhibition in vitro in cow rumen fluid.
  • $590
In Stock
Size
QTY
Raloxifene hydrochloride
Raloxifene HCl, LY156758 hydrochloride, LY156758 (Keoxifene) HCl, LY139481 hydrochloride, Keoxifene hydrochloride
T154982640-04-8
Raloxifene hydrochloride (LY156758 hydrochloride) is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antagonist on mammary gland and uterine tissue.
  • $38
In Stock
Size
QTY
TargetMol | Citations Cited
Ionox 330
BRN 2034522, AO-40, Antioxidant 40, Antioxidant 330, Ahydol
T196331709-70-2
Ionox 330 (Ahydol) is an alkylphenol compound used as an antioxidant.
  • $29
In Stock
Size
QTY
Voglibose
Glustat, Basen, AO 128
T672383480-29-9
Voglibose (Glustat), an N-substituted derivative of valiolamine, exhibits excellent inhibitory activity against α-glucosidases and action against hyperglycemia and various disorders caused by hyperglycemia.
  • $30
In Stock
Size
QTY
Alanyl ornithine
Dipeptide ao-a
T29823643755-41-3
Alanyl ornithine is a dipeptide.
  • Inquiry Price
3-6 months
Size
QTY
Carbazomycin C
T72002108073-62-7
Carbazomycin C is a bacterial metabolite that has been found in Streptomyces and has diverse biological activities. It is active against S. aureus, B. anthracis, B. subtilis, and M. flavus, the fungi T. asteroides and T. mentagrophytes, and P. falciparum. It is also active against a panel of five plant pathogenic fungi. Carbazomycin C is cytotoxic to MCF-7, KB, and NCI H187 cells. It also inhibits 5-lipoxygenase (5-LO) activity in RBL-1 cell extracts.
  • $1,670
6-8 weeks
Size
QTY
AO-1535
T6847587178-48-1
AO-1535 is a semisynthetic monoglycosylceramide derived from O-glycosilated sphingosine. It has been shown to inhibit superoxide production by macrophages suggesting a potential clinical application of AO 1535 in the treatment of inflammatory dermatoses.
  • $1,520
6-8 weeks
Size
QTY
217-AO
T69216470-94-0
217-AO is the tertiary analogue of Phospholine --- a quaternary cholinesterase inhibitor.
  • $1,520
6-8 weeks
Size
QTY
AO-022
T89212
AO-022 is a potent conformational inhibitor of TALDO1. It reduces the protein expression of vimentin and snail, exhibiting antiproliferative and antitumor activities. AO-022 holds potential for use in breast cancer research.
  • $2,370
10-14 weeks
Size
QTY
AO-176
T9901A-17952691109-74-5
AO-176 is a humanized anti-CD47 IgG2 monoclonal antibody. It induces tumor phagocytosis by blocking the interaction between CD47 and SIRPα. AO-176 preferentially binds to tumor cells over normal cells and directly kills tumor cells through a cell-autonomous mechanism, rather than via antibody-dependent cellular cytotoxicity (ADCC). In tumor xenograft models, AO-176 demonstrates dose-dependent antitumor activity. This compound is applicable in cancer research, such as studies involving lymphoma.
  • Inquiry Price
Inquiry
Size
QTY
Losigamone
AO-33, AO33, AO 33, ADD137022;Losigamone, ADD-137022, ADD 137022
T27845112856-44-7In house
Losigamone (AO-33), an agonist of the GABA receptor, can be utilized in studies on the treatment of partial seizures.
  • $75
In Stock
Size
QTY
AOH1996
T775202089314-64-5In house
AOH1996 belongs to small molecule inhibitors and is a PCNA ligand targeting transcription-replication conflicts, with oral activity, metabolic stability, and tumor selectivity. This compound induces transcription-dependent DNA double-strand breaks and apoptosis, and is used for antitumor therapy.
  • $60
In Stock
Size
QTY
TargetMol | Inhibitor Hot
MAO-IN-1
T10079124991-40-8In house
MAO-IN-1 is a potent monoamine oxidase B (MAO B) inhibitor (IC50: 20 nM) for the study of neurologically related diseases.
  • $198
In Stock
Size
QTY
MAO-B-IN-1
T101541124198-17-9In house
MAO-B-IN-1 is a monoamine oxidase B inhibitor and can be used for the research of neurological diseases.
  • $1,520
8-10 weeks
Size
QTY
AOH1160
N-(2-Oxo-2-(2-phenoxyphenylamino)ethyl)-1-naphthamide
T103432089314-57-6In house
AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA). AOH1160 induces apoptosis and causes cell-cycle arrest by interfering with DNA replication.
  • $30
In Stock
Size
QTY
PAOPA
T23121114200-31-6In house
PAOPA belongs to natural product derivatives and serves as an allosteric modulator of the dopamine D2 receptor, possessing the characteristic of promoting binding between high-affinity D2 receptors and agonists. This compound finds application in preclinical studies for schizophrenia and extrapyramidal dysfunction, effectively alleviating behavioral and biochemical abnormalities in rodent models.
  • $148
In Stock
Size
QTY
MAO-B-IN-5
T9759849909-77-9In house
MAO-B-IN-5 is a potent, selective, and orally active MAO-B inhibitor with an IC50 of 0.204 μM, showing potential for research in Parkinson's disease (PD) [1].
  • $155
In Stock
Size
QTY
Fmoc-8-amino-3,6-dioxaoctanoic acid
Fmoc-NH-PEG2-CH2COOH
T15304166108-71-0
Fmoc-8-amino-3,6-dioxaoctanoic acid (Fmoc-NH-PEG2-CH2COOH) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) and a PEG-based PROTAC linker for the synthesis of PROTACs.
  • $29
In Stock
Size
QTY
HDAOS
T1935382692-88-4
HDAOS is utilized in the enzymatic photometric determination of hydrogen peroxide, serving as an optimal reagent for diagnostic assays and biochemical investigations. The resulting purple or blue dye exhibits stability and high absorbance, facilitating substrate quantification.
  • $29
In Stock
Size
QTY
TargetMol | Inhibitor Sale
Kaolin
Hydrated aluminum silicate, HSDB 630, Clay 347, China clay, Bolus alba, Altowhite
T206001332-58-7
Kaolin (Bolus alba) is a clay dominated by minerals of the kaolinite family. Kaolin increased the sensitivity of this method for monitoring hemophilia therapy.
  • $40
In Stock
Size
QTY
hMAO-B-IN-32
Ethyl 7-(diethylamino)-2-oxo-2H-chromene-3-carboxylate
T7823228705-46-6
hMAO-B-IN-32 is a potent hMAO-B selective inhibitor with an IC50 of 45.52 μM.
  • $29
In Stock
Size
QTY
TargetMol | Inhibitor Sale
Cyclohexane-1,2,3,4,5,6-hexaol
Cyclohexane-1,2,3,4,5,6-hexol, Cyclohexane-1,2,3,4,5,6-hexaol
TYD-006926917-35-7
Cyclohexane-1,2,3,4,5,6-hexaol, also known as inositol, is a natural cyclohexane derivative and alcohol compound with biological activity in signal transduction, osmotic pressure regulation, and lipid metabolism, and is widely used in biochemical experiments and drug synthesis research.
  • $29
In Stock
Size
QTY
DAO-IN-2
Fr1408239793-31-2
DAO-IN-2 ,with CAS No. 39793-31-2, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. DAO-IN-2 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.
  • $29
In Stock
Size
QTY
TargetMol | Inhibitor Sale