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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
20 Results for "
inositol phosphates
" in MedChemExpress (MCE) Product Catalog:
Products (20)
20 Results for "inositol phosphates" in MCE Product Catalog:
6
6 Publications Verification
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Calhex 231 hydrochloride is a potent negative allosteric modulator that blocks (IC50 = 0.39 μM) increases in [ 3H]inositol phosphates elicited by activating the human wild-type CaSR transiently Ca 2+-sensing receptor. Calhex 231 hydrochloride can be used in the study of traumatic hemorrhagic shock (THS) and diabetic cardiomyopathy (DCM) .
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1 Cited Publications
Cat. No.: HY-N2581
CAS No.: 14306-25-3
Synonyms: myo-inositol, hexakisdihydrogen phosphate sodium salt; inositol hexaphosphate sodium salt
Category:
Zea mays L. Natural Products Other Diseases Plants Gramineae Extract Disease Research Fields
Target:
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1 Cited Publications
Synonyms: inositol hexaphosphate; SNF472 free acid
Category:
Neurological Disease Food Preservation Research Ketones, Aldehydes, Acids Plants Other Families Extract Endogenous metabolite Disease Research Fields Inflammation/Immunology Agricultural Research
Target:
1
1 Cited Publications
Cat. No.: HY-N2580
CAS No.: 63903-51-5
Target:
1
1 Cited Publications
Cat. No.: HY-W018059
CAS No.: 129832-03-7
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4-Phytase is a type of phytase. Phytase is an enzyme capable of degrading phytic acid into lower inositol phosphates and inositol. Exogenous phytase enhances the utilization of nutrients that are originally bound to phytic acid, thereby reducing the levels of phosphorus, calcium, amino acids, and energy in the diet without compromising animal growth performance, while elevating the apparent ileal digestibility and digestible intake of nutrients to levels comparable to those of nutrient-adequate control groups .
Synonyms: d-Norfenfluramine hydrochloride
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(+)-Norfenfluramine hydrochloride, a major hepatic metabolite of (+)-fenfluramine, is a selective 5-HT2B receptor agonist (Ki: 11.2 nM). (+)-Norfenfluramine hydrochloride potently stimulates the hydrolysis of inositol phosphates and increases intracellular Ca 2+. (+)-Norfenfluramine hydrochloride can be used for the research of primary pulmonary hypertension and valvular heart disease .
Cat. No.: HY-W131725
CAS No.: 19036-73-8
Synonyms: d-Norfenfluramine
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Research Areas:
(+)-Norfenfluramine a major hepatic metabolite of (+)-fenfluramine, is a selective 5-HT2B receptor agonist (Ki: 11.2 nM). (+)-Norfenfluramine potently stimulates the hydrolysis of inositol phosphates and increases intracellular Ca 2+. (+)-Norfenfluramine can be used for the research of primary pulmonary hypertension and valvular heart disease .
Cat. No.: HY-120985
CAS No.: 123000-02-2
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Xestospongins and araguspongins are marine natural products first isolated from Pacific basin sponges, and noted to have vasodilatory properties.1 Inositol phosphates (IP) are important signal transduction messengers acting via IP3 receptors to promote the mobilization of Ca2+ from intracellular stores.2 Araguspongin B antagonizes the calcium-releasing action of inositol 1,4,5-trisphosphate at the receptor level in cerebral microsomes, with an IC50 of 0.6 μM. It is nearly as potent as xestospongin C as an antagonist of the IP3 receptor.
Cat. No.: HY-103320
CAS No.: 652973-93-8
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Research Areas:
Calhex 231 is a potent negative allosteric modulator that blocks (IC50 = 0.39 μM) increases in [ 3H]inositol phosphates elicited by activating the human wild-type CaSR transiently Ca 2+-sensing receptor. Calhex 231 can be used in the study of traumatic hemorrhagic shock (THS) and diabetic cardiomyopathy (DCM) .
Cat. No.: HY-137608
CAS No.: 221010-51-1
Synonyms: UDP-β-S
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Research Areas:
Uridine 5'-O-thiodiphosphate (UDP-β-S) is a P2Y6 receptor agonist with an EC50 of 25 nM. Uridine 5'-O-thiodiphosphate resists degradation by extracellular nucleotidases and stimulates the accumulation of inositol phosphates. Uridine 5'-O-thiodiphosphate stimulates contractile responses in endothelium-denuded rat mesenteric arteries. As a mitogen, Uridine 5'-O-thiodiphosphate stimulates DNA synthesis, [ 3H] thymidine incorporation, protein synthesis, [ 3H]leucine incorporation, and increases the number of vascular smooth muscle cells. Uridine 5'-O-thiodiphosphate can be used in the research of cardiovascular diseases such as atherosclerosis .
Cat. No.: HY-137608A
Synonyms: UDP-β-S trisodium
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Research Areas:
Uridine 5'-O-thiodiphosphate trisodium (UDP-β-S trisodium) is a P2Y6 receptor agonist with an EC50 of 25 nM. Uridine 5'-O-thiodiphosphate trisodium resists degradation by extracellular nucleotidases and stimulates the accumulation of inositol phosphates. Uridine 5'-O-thiodiphosphate trisodium stimulates contractile responses in endothelium-denuded rat mesenteric arteries. As a mitogen, Uridine 5'-O-thiodiphosphate trisodium stimulates DNA synthesis, [ 3H] thymidine incorporation, protein synthesis, [ 3H]leucine incorporation, and increases the number of vascular smooth muscle cells. Uridine 5'-O-thiodiphosphate trisodium can be used in the research of cardiovascular diseases such as atherosclerosis .
Cat. No.: HY-P10270
CAS No.: 147428-10-2
Cat. No.: HY-146873S
CAS No.: 2342575-29-3
Cat. No.: HY-146874S
CAS No.: 2342575-32-8
Cat. No.: HY-181448
Synonyms: inositol hexaphosphate hexalithium; SNF472 hexalithium
Target:
Research Areas:
Cardiovascular Disease Neurological Disease Metabolic Disease Cancer
Phytic acid (Inositol hexaphosphate hexalithium) hexalithium is an orally active compound. Phytic acid hexalithium can be derived from the seeds of legumes. Phytic acid is a [PO4] 3- storage depot and precursor for other inositol phosphates and pyrophosphates. Phytic acid hexalithium attenuates Aβ oligomers and upregulates Autophagy protein. Phytic acid hexalithium can be used in cardiovascular disease, metabolic disease, nervous system disease and cancer research .
Cat. No.: HY-182654B
Cat. No.: HY-182654A
Cat. No.: HY-182654
Cat. No.: HY-103320AR
CAS No.: 2387505-78-2
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Research Areas:
Calhex 231 hydrochloride (Standard) is the analytical standard of Calhex 231 hydrochloride (HY-103320A). This product is intended for research and analytical applications. Calhex 231 hydrochloride is a potent negative allosteric modulator that blocks (IC50 = 0.39 μM) increases in [3H]inositol phosphates elicited by activating the human wild-type CaSR transiently Ca2+-sensing receptor. Calhex 231 hydrochloride can be used in the study of traumatic hemorrhagic shock (THS) and diabetic cardiomyopathy (DCM) .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
