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Results for "

morin

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    30
    TargetMol | All_Pathways
  • Inhibitory Antibodies
    1
    TargetMol | Inhibitory_Antibodies
  • Natural Products
    17
    TargetMol | Natural_Products
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    2
    TargetMol | Recombinant_Protein
  • Reference Standards
    3
    TargetMol | Standard_Products
Morin
Toxylon pomiferum, Calico Yellow, Aurantica, Al-Morin
T2835480-16-0
Morin (Calico Yellow) was found to be a weak inhibitor of fatty acid synthase (IC50: 2.33 μM). Morin is a yellow color substance that can be isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava).
  • $39
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Morin monohydrate
oxylon pomiferum monohydrate, Calico Yellow monohydrate, Aurantica monohydrate, Al-Morin monohydrate
T65966202-27-3
Morin monohydrate (oxylon pomiferum monohydrate) is a flavonoid extracted from Morus alba plant with anticancer, antioxidant, and anti-inflammatory activities, which reduces T-2 toxin-induced TNF-alpha, COX-2, IL-1β, IL-6, caspase-1, caspase-3, and caspase-11 mRNA. BML-286 is a WNP-containing WNP-containing BML-286, which reduces T-2 toxin-induced TNF-α, COX-2, IL-1β, IL-6, caspase-1, caspase-3, and caspase-11 mRNA expression, and ameliorates T-2 toxin-induced injury by decreasing malondialdehyde (MDA) and increasing superoxide dismutase (SOD), catalase (CAT), glutathione (GSH), and glutathione peroxidase (GSH-PX).
  • $38
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TargetMol | Citations Cited
Morin 3-O-β-D-glucopyranoside
T755011169766-14-6
Morin 3-O-β-D-glucopyranoside, a natural flavonoid, exhibits antifungal, anticancer, and antioxidant properties. This compound also inhibits reverse transcriptase, protein-tyrosine kinase, and xanthine oxidase, while demonstrating anti-HIV, antiarteriosclerotic, and superoxide scavenging activities [1].
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Morin dihydrate
T124483
Morin dihydrate is a useful organic compound for research related to life sciences and the catalog number is T124483.
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Morin (Standard)
TMSM-2747480-16-0
Morin (Standard) is a reference standard for research and analysis in studies involving Morin. Morin (Calico Yellow) was found to be a weak inhibitor of fatty acid synthase (IC50: 2.33 μM). Morin is a yellow color substance that can be isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava).
  • $458
7-10 days
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Morinidazole (R enantiomer)
R-Morinidazole
T12096898230-59-6
Morinidazole (R enantiomer) is the R-enantiomer of Morinidazole.
  • $30
5 days
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Morinidazole
T12096L92478-27-8
Morinidazole shows antibacterial activity and can be used in studies about bacterial infections research such as appendicitis and pelvic inflammatory disease caused by anaerobic bacteria.
  • $33
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Oxotremorine M iodide
Oxotremorine methiodide
T123393854-04-4
Oxotremorine M iodide (Oxotremorine methiodide) is an agonist of mAChR and potentiates NMDA receptors.
  • $43
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Artemorin
T12448064845-92-7
Artemorin is a useful organic compound for research related to life sciences. The catalog number is T124480 and the CAS number is 64845-92-7.
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Morindin
T124563
Morindin is a useful organic compound for research related to life sciences and the catalog number is T124563.
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15alpha-Hydroxyculmorin
T130700
15alpha-Hydroxyculmorin is a useful organic compound for research related to life sciences and the catalog number is T130700.
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MORINDONE
T202844478-29-5
MORINDONE, an anthraquinone compound, exhibits significant binding affinity towards multiple targets including β-catenin, MDM2-p53, and KRAS. It displays notable cytotoxicity and selective activity against colorectal cancer cell lines, and effectively downregulates the expression of mutated TP53 and KRAS genes.
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10-14 weeks
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Oxotremorine
T20325170-22-4
Oxotremorine acts as an agonist of mAChR, specifically activating the M1 and M3 acetylcholine receptors. In drug discrimination experiments with macaques, it exhibits effects similar to nicotine.
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10-14 weeks
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Tremorine
T20754951-73-0
Tremorine is an agent that induces tremors in animals. It is used to create animal tremor models for Parkinson's disease research.
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10-14 weeks
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Oxotremorine sesquifumarate
T2311617360-35-9
Oxotremorine sesquifumarate is a muscarinic agonist.
  • $57
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3-Hydroxymorindone (Standard)
TMSM-3751
3-Hydroxymorindone (Standard) is a reference standard of 3-Hydroxymorindone intended for quantitative analysis, quality control, and related biochemical research applications.
  • $678
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Morindin (Standard)
TMSM-413560450-21-7
Morindin (Standard) is a reference standard of Morindin intended for quantitative analysis, quality control, and related biochemical research applications.
  • $1,560
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4-O-Alpha-L-Rhamnopyranosylglucosinalbin; Glucomoringin
TN1181474542-19-1
4-O-Alpha-L-Rhamnopyranosylglucosinalbin; Glucomoringin is a high-purity biochemical reagent suitable for biochemical experiments and drug synthesis research.
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4-6 weeks
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4"-O-Acetylglucomoringin
TN11815549503-17-5
4"-O-Acetylglucomoringin is a high-purity biochemical reagent suitable for biochemical experiments and drug synthesis research.
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4-6 weeks
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3-hydroxymorindone
TN125380368-74-7
3-hydroxymorindone is a natural product from Morinda citrifolia. 3-hydroxymorindone is a pigment.
  • $83
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Dihydromorin
TN158318422-83-8
trans-Dihydromorin is an effective hypopigmenting agent in normal skin cells, hypopigmenting agents effective in melanoma system may not be effective on normal melanocytes, indicating that a non-tumor melanocyte system is more suitable for the screening o
  • $1,260
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1,5,15-Tri-O-methylmorindol
TN2500942609-65-6
1,5,15-Tri-O-methylmorindol has effects against the Epstein-Barr virus early antigen (EBV-EA) activation induced by TPA.
  • $660
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Moringin
TN458373255-40-0
Moringin is an isothiocyanate obtained from myrosinase-mediated hydrolysis of the glucosinolate precursor glucoMoringin present in Moringa oleifera seeds. Moringin has anti-inflammatory and antioxidative properties.
  • $118
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Acremorin E
TN9022
Acremorin E (Compound 7) is a terpene compound with antifungal properties. It exhibits activity against C. gattii (MIC: 8 μg/mL) by enhancing ribosome biosynthesis and RNA-binding gene expression, while inhibiting RNA, nucleic acid metabolism, and ATPase activity.
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