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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
35 Results for "
placenta
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "placenta" in MCE Product Catalog:
1
1 Cited Publications
Cat. No.: HY-P74627A
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PGF; PlGF-2; Prev. PGFL; placental Growth Factor, Vascular Endothelial Growth Factor-Related Protein; PLGF; placental Growth Factor, Vascular Endothelial Growth Factor-Related Protein, Isoform CRA_a; placenta Growth Factor; placental Growth Factor-Like; S
Species:
Human
Source:
E. coli
1
1 Cited Publications
Cat. No.: HY-P74626
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PGF; PlGF-2; Prev. PGFL; placental Growth Factor, Vascular Endothelial Growth Factor-Related Protein; PLGF; placental Growth Factor, Vascular Endothelial Growth Factor-Related Protein, Isoform CRA_a; placenta Growth Factor; placental Growth Factor-Like; S
Species:
Human
Source:
HEK293
1
1 Cited Publications
Cat. No.: HY-P70246
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FTH1; Proliferation-Inducing Protein 15; Prev. FTHL6; Ferritin, Heavy Polypeptide 1; FTH; Ferritin H Subunit; Ferritin Heavy Chain; Apoferritin; PIG15; H-Ferritin; PLIF; Ferritin; FHC; NBIA9; Cell Proliferation-Inducing Gene 15 Protein; HFE5; Ferritin Heavy Chain 1; placenta Immunoregulatory Factor
Species:
Human
Source:
E. coli
Cat. No.: HY-P11101
CAS No.: 2294870-89-4
Target:
Research Areas:
Target:
Research Areas:
YM511 is a highly specific non-steroidal aromatase inhibitor. YM511 inhibits aromatase activities in microsomes from rat ovary and human placenta competitively (IC50s of 0.4 and 0.12 nM, respectively). YM511 slightly inhibits production of other steroid hormones. YM511 has the potential for suppressing estrogen-dependent action research without affecting serum levels of other steroid hormones .
Cat. No.: HY-106915
CAS No.: 143162-65-6
Synonyms: SPR 210
Target:
Research Areas:
SG-210 (SPR 210) is an orally active and selective aldose reductase (AR) inhibitor. SG-210 has IC50 values of 9.5 nM and 10 nM for AR from porcine lens and human placenta, respectively. SG-210 can inhibit sorbitol accumulation and ameliorate diabetic neuropathy and retinopathy in Streptozotocin (HY-13753)-induced diabetic rats. SG-210 can be used in the research of diseases such as diabetes-related complications .
Cat. No.: HY-174734
Target:
Research Areas:
Human CSF1 mRNA encodes the human colony stimulating factor 1 (CSF1) protein, a cytokine that controls the production, differentiation, and function of macrophages. CSF1 may be involved in the development of the placenta.
Cat. No.: HY-155234
Target:
Research Areas:
Steroid sulfatase-IN-6 (Compound 10c) is an irreversible inhibitor of steroid sulfatase (STS). Steroid sulfatase-IN-6 has an Ki value of 0.4 nM for human placenta STS. Steroid sulfatase-IN-6 can be used for tumor diseases research .
Cat. No.: HY-W424918
CAS No.: 316-07-4
Target:
Research Areas:
Opromazine hydrochloride is an antipsychotic medication that exhibits sedative and antiemetic pharmacological effects, making it effective for treating psychiatric disorders such as schizophrenia and psychosis. Opromazine hydrochloride functions by reducing dopaminergic activity through the blockade of dopamine receptors in the brain. Opromazine hydrochloride has been analyzed for its metabolites in various microsomal enzymes, revealing differences in formation rates that underscore the variability of drug-metabolizing enzymes in human liver and placenta microsomes.
Cat. No.: HY-P2524
CAS No.: 160295-81-8
Target:
Research Areas:
Cat. No.: HY-P70833
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: INSL4; Insulin-Like Peptide 4; Insulin Like 4; Early placenta Insulin-Like Peptide (EPIL); EPIL; PLACENTIN; Early placenta Insulin-Like Peptide; Placentin; Insulin-Like 4 (placenta)
Species:
Human
Source:
HEK293
(E)-4-Stilbenol is a hydroxylated stilbene compound and also a fungicide. (E)-4-Stilbenol inhibits the growth of Gloeophyllum trabeum and Poria placenta. (E)-4-Stilbenol is applicable to research related to fungal infections .
Cat. No.: HY-17417E
CAS No.: 65700-73-4
Target:
Research Areas:
(+)-Naloxone is a TLR4 inhibitor and the dextrorotatory enantiomer of the non-opioid Naloxone (HY-17417A) that lacks opioid receptor binding activity. (+)-Naloxone binds to MD2, preventing LPS from binding to TLR4, thereby inhibiting TLR4 signaling, downstream NFκB activation, and proinflammatory cytokine synthesis. (+)-Naloxone crosses the placenta. (+)-Naloxone is used in the research of preterm birth .
Cat. No.: HY-105184R
CAS No.: 148869-05-0
Target:
Research Areas:
YM511 (Standard) is the analytical standard of YM511 (HY-105184). This product is intended for research and analytical applications. YM511 is a highly specific non-steroidal aromatase inhibitor. YM511 inhibits aromatase activities in microsomes from rat ovary and human placenta competitively (IC50s of 0.4 and 0.12 nM, respectively). YM511 slightly inhibits production of other steroid hormones. YM511 has the potential for suppressing estrogen-dependent action research without affecting serum levels of other steroid hormones .
Cat. No.: HY-183407
CAS No.: 50648-52-7
Target:
Research Areas:
R 8231 is a reversible inhibitor of Alkaline Phosphatase. R 8231 potently inhibits alkaline phosphatases derived from human liver, bone, kidney and spleen, while exerts weak effects on those derived from human intestine and placenta. The IC50 value of R 8231 for inhibiting bone alkaline phosphatase from adult rabbits is approximately 1 μM, whereas that for inhibiting chicken bone alkaline phosphatase is approximately 100 μM. R 8231 can be used for alkaline phosphatase histochemistry, phosphatase activity identification and bone metabolism-related studies .
Cat. No.: HY-E72103
Target:
Research Areas:
Human CYP1A1, Reductase+b5 refers to a near-physiological recombinant microsomal system co-expressed in insect cells, consisting of human cytochrome P450 1A1, NADPH-P450 oxidoreductase (CPR) and cytochrome b5. Human CYP1A1 is a human cytochrome P450 subtype belonging to the CYP1 family, as well as a major metabolic enzyme. Its expression is concentrated in tissues such as lung, breast, placenta and endometrium, and it can metabolize polycyclic aromatic hydrocarbons and estrogens into carcinogenic intermediates with DNA-damaging activity .
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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
