Cat. No. | Product Name | Field of Application | Chemical Structure |
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DC40427 | Tachysterol 3 |
Tachysterol 3 is a side product in vitamin D photosynthesis.
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DC40426 | Previtamin D3 |
Previtamin D3 is an intermediate in the production of cholecalciferol (vitamin D3).
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DC40424 | 24(28)-Dehydroergosterol |
24(28)-Dehydroergosterol is a derivative of Episterol. Episterol is a sterol involved in the biosynthesis of steroids.
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DC40417 | Ferrous bisglycinate |
Ferrous bisglycinate is an orally active iron fortificants and therapeutic iron supplements. Ferrous bisglycinate can be used for the research of iron deficiency anemia.
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DC40410 | α-Tocotrienol |
α-Tocotrienol is an isoform of vitamin E and found in vegetables, fruits, seeds, nuts, grains, and oils. Vitamin E plays a role as an antioxidant, in lowering cholesterol and other lipids, as a neuroprotective and anticancer agent, and in cardiovascular disease protection.
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DC40406 | Magnesium glycinate |
Magnesium glycinate (Magnesium bisglycinate), the magnesium salt of glycine, is a nutrient supplement. Magnesium glycinate has satisfactory physico-chemical properties and bioactivities. Metal glycinate chelates are formed by glycine and metal compounds through chemical reactions. Magnesium is an essential mineral that plays a critical role in the human body. Magnesium takes part in the process of energy metabolism and assists the maintenance of normal muscle function.
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DC40394 | Kgp-IN-1 hydrochloride |
Kgp-IN-1 hydrochloride is an arginine-specific gingipain (Rgp) inhibitor extracted from patent WO2017201322A1, compound 13-R.
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DC40388 | Benzyldimethylstearylammonium chloride |
Benzyldimethylstearylammonium chloride, a quarternary ammonium compound, exerts no selective embryopathic activity.
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DC40387 | Carboprost |
Carboprost (15(S)-15-Methyl Prostaglandin F2α) is a metabolically stable synthetic analog of prostaglandin F2α. Carboprost stimulates uterine contractions and induces abortion. Carboprost is used for postpartum hemorrhage due to uterine atony and for the termination of pregnancy in the second trimester.
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DC40385 | 6-Chloro-7-hydroxy-4-methylcoumarin |
6-Chloro-7-hydroxy-4-methylcoumarin (compound 3) an intermediate of pharmaceutical synthesis.
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DC40384 | 2,2-Dihydroxy-1-phenylethan-1-one |
2,2-Dihydroxy-1-phenylethan-1-one (compound 2d) is an intermediate of pharmaceutical synthesis with antioxidant property.
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DC40383 | L-Gulose |
L-Gulose, the putative furanose form of L-sorbosone, is an L-hexose sugar and an intermediate in the biosynthesis of L-Ascorbate (vitamin C).
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DC40380 | Labetalone hydrochloride |
Labetalone hydrochloride is an impurity of Labetalol. Labetalol is an orally active adrenoceptor blocking drug which is a competitive antagonist at both alpha- and beta-adrenoceptor sites.
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DC40377 | SPL-410 |
SPL-410 is an orally active, highly potent and selective hydroxyethylamine based SPPL2a (Signal Peptide Peptidase Like 2a) inhibitor, with an IC50 of 9 nM.
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DC40374 | AG-09/1 |
AG-09/1 is a specific formyl peptide receptor 1 (FPR1) agonist. N-formyl peptide receptors (FPR) are important in host defense.
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DC40372 | Maltoheptaose |
Maltoheptaose is an activator of phosphorylase B to prepare heptulose-2-phosphate. Maltoheptaose is a maltooligosaccharide contanins seven glucose units.
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DC40356 | Lupeol acetate |
Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B.
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DC40354 | (S)-Praziquantel D11 |
(S)-Praziquantel D11 is the deuterium labeled (S)-Praziquantel. (S)-Praziquantel, a toxic enantiomerof Praziquantel, is ineffective against worms.
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DC40348 | Pseudoginsenoside Rh2 |
Pseudoginsenoside Rh2, synthesized from Ginsenoside Rh2, possesses anti-cancer activitied.
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DC40345 | 5(S)-HPETE |
5(S)-HpETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of 5-LO on arachidonic acid. 5(S)-HpETE is metabolized to leukotriene A4 (LTA4), a key intermediate in the formation of LTs.
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DC40323 | JMS-17-2 hydrochloride |
JMS-17-2 hydrochloride is a potent and selective CX3CR1 antagonist with an IC50 of 0.32 nM. JMS-17-2 hydrochloride impairs metastatic seeding and colonization of breast cancer cells.
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DC40322 | 5-Hydroxymebendazole D3 |
5-Hydroxymebendazole D3 is a deuterium labeled 5-Hydroxymebendazole. 5-Hydroxymebendazole is the one metabolite of Benzimidazoles.
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DC40316 | Fenpropathrin |
Fenpropathrin is a synthetic pyrethroid insecticide in agriculture. Fenpropathrin may induces parkinsonian symptoms progressively.
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DC40311 | 12(S)-HETE D8 |
12(S)-HETE D8 contains eight deuterium atoms at the 5, 6, 8, 9, 11, 12, 14 and 15 positions. It is intended for use as an internal standard for the quantification of 12(S)-HETE by GC- or LC-mass spectrometry (MS). 12(S)-HETE D8 is the predominant lipoxygenase product of mammalian platelets. It enhances tumor cell adhesion to endothelial cells, fibronectin, and the subendothelial matrix at 0.1 μM.
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DC40308 | Symphytine |
Symphytine is a pyrrolizidine alkaloid isolated from Symphytum officinale and has carcinogenicity.
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DC40303 | δ-Tocotrienol |
δ-Tocotrienol is a Vitamin E in vegetables, fruits, seeds, nuts, grains and oils. Vitamin E has become well known for its role as an antioxidant, in lowering cholesterol and other lipids, as a neuroprotective and anticancer agent, and in cardiovascular disease protection.
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DC40299 | (±)-Jasmonic acid |
(±)-Jasmonic acid is a plant growth regulator and a derivative of α-linolenic acid. (±)-Jasmonic acid decreases chlorophyll levels in green and etiolated barley leaf segments and inhibits elongation of rice seedlings.
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DC40298 | 1'-Hydroxy bufuralol |
1'-Hydroxy bufuralol, the main metabolite of bufuralol, can reflect CYP2D activity.
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DC40297 | Erythromycin A enol ether |
Erythromycin A enol ether is an acidic degradation product of Erythromycin A (macrolide antibiotic) and has no antibacterial effect.
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DC40292 | 1-Oxo Ibuprofen |
1-Oxo Ibuprofen (Ibuprofen EP impurity J) is a degradation product and a potential impurity in preparations of Ibuprofen. Ibuprofen is an anti-inflammatory inhibitor targeting COX-1 and COX-2 with IC50s of 13 μM and 370 μM, respectively.
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