成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Polyoxyethylene 40 stearate

  Cat. No.:  DC23907   Featured
Chemical Structure
9004-99-3
For research use only. We do not sell to patients.
We match the best price and quality on market.
Email:order@dcchemicals.com  sales@dcchemicals.com
Tel:+86-021-58447131
We are official vendor of:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
More than 5000 active chemicals with high quality for research!
Field of application
A non-ionic emulsifying agent that can modulate multidrug resistance and enhances antitumor activity of vinblastine sulfate by modulating substrate-stimulated P-gp ATPase activity.
Cas No.: 9004-99-3
Chemical Name: Polyoxyethylene stearate
Synonyms: polyoxyethylene 8 stearate;Polyethylene glycol monostearate;MYRJ(TM) 53;MYRJ(TM) 59;MYRJ 58;MYRJ 59;MYRJ(R) 53;MYRJ(TM) 45;MYRJ 45;PEG 200 STEARATE;Polyoxyethylene stearate;PEG1000monostearate;PEG1540monostearate;PEG300monostearate;PEG4000monostearate;PEG400monostearate;PEG600monostearate;POES;Poly(oxy-1,2-ethanediyl), .α.-hydro-.ω.-hydroxy-, octadecanoate;Polyethylene Glycol Monostearate (10E.O.);Polyethylene Glycol Monostearate (25E.O.);Polyethylene Glycol Monostearate (55E.O.);POLYETHYLENE GLYCOL MONOSTEARATE N-4 (PALMITATE AND STEARATE MIXTURE);Polyethylene Glycol Monostearate(45E.O.);n≈10;n≈100;n≈25;PEG-100 stearate;PEG-32 stearate;PEG-6 stearate;PEG-8 stearate;PEG-75 stearate;Myrj 52;PEG monostearate;ENaC alpha Antibody;2-Hydroxyethyl stearate;Glycol stearate;2-Hydroxyethyl octadecanoate;Ethylene glycol monostearate;Cremophor A;Cerasynt M;Clearate G;Cerasynt MN;Cithrol PS;Polyoxyl 40 stearate;Polystate;Lactine;Myrj;Cithrol 10MS;Cerasynt 660;Polystate B;Prodhybase P;Akyporox S 100;PEG stearate;Soromin-SG;Lamacit CA;Emerest 2640;Stearoks 6;Stearoxa-6;Stearox 6;Nikkol MYS;Pegosperse S 9;Glycol monostearate;Emanon 3113;Stenol 8;Emcol H 35-A;Arosurf 1855E40;Polyoxyl（40）Stearate
SMILES: O(C([H])([H])C([H])([H])O[H])C(C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])=O
Formula: C20H40O3
M.Wt: 328.5298
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: A non-ionic emulsifying agent that can modulate multidrug resistance and enhances antitumor activity of vinblastine sulfate by modulating substrate-stimulated P-gp ATPase activity; inhibits P-gp mediated efflux in a concentration-dependent manner in Caco-2 cells, also shows potential inhibitory activitites agasint CYP2C9 and CYP2C19.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC31074 Isopropyl myristate Isopropyl myristate is the ester of isopropyl alcohol and myristic acid.
DC75868 AZ14133346 AZ14133346 (compound 36) is a potent and selective inhibitor of EGFR Exon20 insertions, with the IC50 of 85 nM. AZ14133346 plays an important role in cancer research.
DC75865 TI17 ??TI17?? represents a novel class of targeted anticancer agents that specifically disrupt DNA damage repair mechanisms in malignant cells.
DC75816 Nisoxetine Nisoxetine acts as a highly selective and potent noradrenaline transporter (NET) antagonist, exhibiting a binding affinity (Kd) of 0.76 nM. In addition to its antidepressant properties, nisoxetine functions as a local anesthetic by inhibiting voltage-gated sodium channels. This dual pharmacological activity makes it a compound of interest for both neurological and pain management research.
DC75202 Fosaprepitant free acid Fosaprepitant, also known as MK0517, is an antiemetic drug, administered intravenously. It is a prodrug of aprepitant. Fosaprepitant was developed by Merck & Co. and was approved. It is a prodrug of Aprepitant. It aids in the prevention of acute and delayed nausea and vomiting associated with chemotherapy treatment. Fosaprepitant is a weak inhibitor of CYP3A4, and aprepitant, the active moiety, is a substrate, inhibitor, and inducer of CYP3A4
DC74684 ZH8667 ZH8667 is a trace amine-associated receptor 1 (TAAR1)–Gs agonist.
DC74646 EB-PSMA-617 EB-PSMA-617 is an Evans blue-modified prostate-specific membrane antigen (PSMA) 617 ligand for making 177Lu-EB-PSMA, which is potential useful for Metastatic Castration-Resistant Prostate Cancer.
DC74641 HC-258 HC-258 is a Covalent Acrylamide TEAD Inhibitor That Reduces Gene Expression and Cell Migration. HC-258 reduces the CTGF, CYR61, AXL, and NF2 transcript levels and inhibits the migration of MDA-MB-231 breast cancer cells. Co-crystallization with hTEAD2 confirmed that HC-258 binds within TEAD’s PA pocket, where it forms a covalent bond with its cysteine.
DC74639 Oligopeptide-10 Oligopeptide-10, also known as granactive oligopeptide-10, is a synthetic bio-active peptide composed of 15 amino acids. it can help manage acne-causing bacteria, both on its own and in conjunction with anti-acne superstar exfoliant salicylic acid.
DC74638 GLPG3667 GLPG3667 is an oral, reversible, and selective tyrosine kinase 2 (TYK2) inhibitor. It is being developed to treat inflammatory and auto-immune diseases. Biochemical assays showed that GLPG3667 displayed nanomolar potency on TYK2 with a selectivity over other JAK kinases >3-fold. In human PBMC, GLPG3667 showed comparable potency on the IFNα and IL-23 pathways (around 50 nM). Selectivity for TYK2 on the IFNα pathway was >14-fold and >19-fold toward the IL-2 and GM-CSF pathways in human PBMC and whole blood, respectively. Dermal ear inflammation in a mouse model of psoriasis driven by IL-23 was prevented by GLPG3667 with a minimal effective dose of 3 mg/kg given orally once daily. This effect was associated with a decrease in neutrophil infiltration and STAT3 phosphorylation at sites of inflammation. In healthy HV, GLPG3667 completely inhibited IFNα-induced STAT1 and STAT3 phosphorylation but did not impact IL-2- and GM-CSF-induced STAT5 phosphorylation.
X