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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC47096 | Umckalin |
Umckalin is a oxygenated coumarin from Pelargonium sidoides.
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| DC47086 | 7,3′,4′-Tri-O-methyleriodictyol |
7,3′,4′-Tri-O-methyleriodictyol is a flavonoid with an antimutagenic activity. 7,3′,4′-Tri-O-methyleriodictyol inhibits the furylfuramide-induced SOS response and has potency as bioantimutagens.
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| DC47085 | AZD-CO-Ph-PEG4-Ph-CO-AZD |
AZD-CO-Ph-PEG4-Ph-CO-AZD is a bis-β-lactam linker can be used for antibody-siRNA conjugate synthesis.
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| DC47083 | Exaluren |
Exaluren (ELX-02) is an synthetic eukaryotic ribosome-selective glycoside that induces read through of nonsense mutations, resulting in normally localized full-length functional proteins. Exaluren is used for the research of cystic fibrosis caused by nonsense mutations.
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| DC47079 | Valiloxibic acid |
Valiloxibic acid is a prodrug of γ-Hydroxybutyric acid (GHB).GHB is a naturally occurring neurotransmitter and a psychoactive drug, it acts on the GHB receptor and is a weak agonist at the GABAB receptor.
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| DC47078 | Umifoxolaner |
Umifoxolaner is an anti-parasitic agent (veterinary).
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| DC47076 | Udonitrectag |
Udonitrectag (REC 0559), a low molecular weight compound that mimics NGF, aims to address the issue of NGF stability.
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| DC47075 | Syringetin |
Syringetin, a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts.
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| DC47073 | Relzomostat |
Relzomostat is a methionine aminopeptidase 2 (MetAP2) inhibitor.Relzomostat may be useful for the research of obesity, type 2 diabetes, and other obesity-associated conditions.
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| DC47070 | Polyketide synthase 13-IN-1 |
Polyketide synthase 13-IN-1 (compound 32) is a polyketide synthase 13 inhibitor.
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| DC47068 | Milategrast |
Milategrast is useful as cell adhesion inhibitor or cell infiltration inhibitor. Milategrast in vitro inhibites the adhesion of Jurkat cells to human fibronectin with an IC50 of <5 μM.
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| DC47067 | Luvadaxistat |
TAK-831 is a highly selective and potent inhibitor of D-amino acid oxidase (DAAO) and can be used in studies of schizophrenia.
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| DC47065 | Idetrexed |
Idetrexed is a thymidylate synthase inhibitor specifically transported into alpha-folate receptor (alpha-FR)-overexpressing tumors. BGC 945 inhibited thymidylate synthase with a Ki of 1.2 nmol/L.
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| DC47064 | Hexasodium phytate |
Hexasodium phytate (Phytic acid hexasodium) is a phosphorus storage compound of seeds and cereal grains. Hexasodium phytate has a strong ability to chelate multivalent metal ions, specially zinc, calcium, iron and as with protein residue. Hexasodium phytate inhibits the enzymatic superoxide source xanthine oxidase (XO), and has antioxidative, neuroprotective, anti-inflammatory effects.
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| DC47061 | ARN 077 (enantiomer) |
ARN 077 enantiomer (19) is the less active enantiomer of ARN 077, with an IC50 of 3.53 μM for rat NAAA.
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| DC47047 | Polθ-IN-1-d3 |
Polθ-IN-1-d3 (example 1) is a deuterated Polθ inhibitor used for cancer study (extracted from patent WO2021028670).
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| DC47028 | Sec61-IN-3 |
Sec61-IN-2 (A3) is a protein secretion inhibitor (extracted from patent WO2020176863).
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| DC47027 | Ezurpimtrostat |
Ezurpimtrostat (compound 2-2) is used for the study of fibrosis, cancer, autophagy and cathepsins B (CTSB), L (CTSL) and D (CTSD) related diseases (extracted from patent WO2020048694 A1).
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| DC47026 | 4-Phenyl-7,8-dihydroxycoumarin |
4-Phenyl-7,8-dihydroxycoumarin is a coumarin derivative and can be used for bronchiectasiss research.
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| DC47024 | Ivospemin |
Ivospemin is an antineoplastic spermine analog.
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| DC47023 | Lenalidomide-C10-OH |
Lenalidomide-C10-OH (6a) is an intermediate in the synthesis of INY-03-041.
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| DC47022 | Quercetin 3,3'-dimethyl ether |
Quercetin 3,3'-dimethyl ether possesses antioxidant acticity.
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| DC47021 | Sec61-IN-2 |
Sec61-IN-2 (A347) is a protein secretion inhibitor (extracted from patent WO2020176863).
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| DC47020 | Sophoramine |
Sophoramine ((-)-Sophoramine), an alkaloid, is a dehydro-derivative of Matrine.
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| DC47019 | Sucunamostat |
Sucunamostat is an L-aspartic acid enteropeptidase inhibitor.
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| DC47016 | Yadanzioside M |
Yadanzioside M is a natural compound with anti-cancer activity.
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| DC47015 | D-(+)-Fucose |
D-(+)-Fucose is a nonmetabolizable analogue of l-arabinose. D-(+)-Fucose prevents growth of Escherichia coli B/r on a mineral salts medium plus l-arabinose by inhibiting induction of the l-arabinose operon. D-fucose is a potent inducer of beta-methylgalactoside permease (MGP).
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| DC47012 | Valethamate bromide |
Valethamate bromide is an ester and is a potent rapidly acting anticholinergic spasmolytic and musculotropic agent which accelerates labor by improving cervical dilation.
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| DC47010 | Astragenol |
Astragenol is an intermediate used for Astragenol derivative synthesis. Astragenol derivatives are promising anti-inflammatory agents for prostate cancer research.
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| DC47007 | 3,3'-Diethyloxacarbocyanine iodide |
3,3'-Diethyloxacarbocyanine iodide is a microviscosity probe for micelles and microemulsions.
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