1. Vitamin D Related/Nuclear Receptor Others Metabolic Enzyme/Protease Neuronal Signaling Cell Cycle/DNA Damage Stem Cell/Wnt PI3K/Akt/mTOR Immunology/Inflammation Apoptosis MAPK/ERK Pathway NF-κB Autophagy
  2. Akt Indoleamine 2,3-Dioxygenase (IDO) NF-κB p38 MAPK Reactive Oxygen Species (ROS) Monoamine Oxidase PPAR Environmental Pollutants Mitophagy Apoptosis JNK Isotope-Labeled Compounds ERK PI3K
  3. Triphenyl phosphate-d15

Triphenyl phosphate-d15  (Synonyms: Celluflex TPP-d15; DHPF 005-d15; Disflamol TP-d15; Disflamoll TP-d15; NSC 57868-d15; Phenyl phosphate ((PhO)3PO)-d15; Phoscon FR 903N-d15)

Cat. No.: HY-Y1322S Purity: 99.55%
Handling Instructions Technical Support

Triphenyl phosphate-d15 is the deuterium labeled Triphenyl phosphate. Triphenyl phosphate is an orally active, blood-brain barrier-permeable aryl organophosphate flame retardant and endocrine disruptor. Triphenyl phosphate disrupts mitochondrial dynamic balance through oxidative stress, induces excessive mitophagy and apoptosis, and ultimately leads to myocardial fibrosis. In the brain, Triphenyl phosphate activates the NF-κB inflammatory pathway by disrupting the gut microbiota, alters tryptophan metabolism and elevates neurotoxins, thereby inducing anxiety- and depression-like behaviors. In the skeletal and reproductive systems, Triphenyl phosphate inhibits osteoblast differentiation and induces germ cell apoptosis by suppressing the MAPK/ERK pathway and activating the JNK signal, respectively. In adipose and placental tissues, Triphenyl phosphate promotes lipid accumulation by activating the PI3K/AKT-PPARγ axis, and disrupts placental metabolism via the MAOA/ROS/NF-κB cascade, impairing neurodevelopment of offspring.

For research use only. We do not sell to patients.

Triphenyl phosphate-d<sub>15</sub>

Triphenyl phosphate-d15 Chemical Structure

CAS No. : 1173020-30-8

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Based on 1 publication(s) in Google Scholar

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Description

Triphenyl phosphate-d15 is the deuterium labeled Triphenyl phosphate. Triphenyl phosphate is an orally active, blood-brain barrier-permeable aryl organophosphate flame retardant and endocrine disruptor. Triphenyl phosphate disrupts mitochondrial dynamic balance through oxidative stress, induces excessive mitophagy and apoptosis, and ultimately leads to myocardial fibrosis. In the brain, Triphenyl phosphate activates the NF-κB inflammatory pathway by disrupting the gut microbiota, alters tryptophan metabolism and elevates neurotoxins, thereby inducing anxiety- and depression-like behaviors. In the skeletal and reproductive systems, Triphenyl phosphate inhibits osteoblast differentiation and induces germ cell apoptosis by suppressing the MAPK/ERK pathway and activating the JNK signal, respectively. In adipose and placental tissues, Triphenyl phosphate promotes lipid accumulation by activating the PI3K/AKT-PPARγ axis, and disrupts placental metabolism via the MAOA/ROS/NF-κB cascade, impairing neurodevelopment of offspring.

Application

1. This compound can be used as a tracer.
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.

In Vitro

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

341.38

Formula

C18D15O4P

CAS No.
Unlabeled CAS
Appearance

Solid

Color

White to off-white

SMILES

[2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1OP(OC2=C([2H])C([2H])=C([2H])C([2H])=C2[2H])(OC3=C([2H])C([2H])=C([2H])C([2H])=C3[2H])=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Store at room temperature 3 years

In solvent -80°C 2 years
-20°C 1 year
Purity & Documentation

Purity: 99.74%

References
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