Fingolimod (FTY720) HCl - 10mM in DMSO , Sphingosine 1-phosphate receptor agonist, CAS No.162359-56-0, Sphingosine 1-phosphate receptor agonist

CAS: 162359-56-0 Cat. No.: F407915 Molecular Weight: 343.93 EC Number: 680-631-1
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GRADE & PURITY 10mM in DMSO
Synonyms
2-(4-octylphenethyl)-2-aminopropane-1,3-diol hydrochloride
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
F407915-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Fingolimod (FTY720) HCl Fingolimod (FTY720) HCl is a S1P antagonist with IC50 of 0.033 nM in K562, and NK cells.
In vitro

The inhibitory effect of S1P is revered by various concentrations of FTY720, with IC50 effect of 173 nM. In addition, FTY720 (10 nM) alone exerts no effect on the expression of co-stimulatory molecules. FTY720 reverses the increased expression of HLA-I induced by S1P for both the percentages of cells and the MFI, upon comparing the effect of S1P to the effect of combining S1P with FTY720. Medium and high-dose FTY720-P also enhances the levels of TGF-β1. TGF-β1 and Foxp3 mRNA expression are upregulated in the high-dose FTY720-P group. The proliferation of effector T cells is suppressed significantly in the medium and high-dose FTY720-P group at a Treg/Teff cell ratio of 1:1. At a ratio of 1:1, the proliferation of effector T cells is also suppressed in the high-dose FTY720 group.

In vivo

FTY720 is effective in Ph+ but not Ph- ALL xenografts using an early disease model. FTY720 produces a significant reduction in disease burden in the Ph+ ALL xenografts using an early disease model. Ph+ human ALL xenografts responds to FTY720 with an 80 % reduction in overall disease if treatment has been initiated early on. In contrast, treatment of mice with FTY720 does not result in reduced leukemia compared to controls using four separate human Ph- ALL xenografts.
Cell Data

cell lines:Abl-MLV, Rat 2, KU812, K562, and MEG-01 cells

Concentrations:10 nM

Incubation Time:4 hours

Powder Purity:≥99%

Specifications

Synonyms
2-(4-octylphenethyl)-2-aminopropane-1, 3-diol hydrochloride
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Fingolimod (FTY720) HCl is a S1P antagonist with IC50 of 0.033 nM in K562, and NK cells.
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
AGONIST
Mechanism of action
Sphingosine 1-phosphate receptor agonist
Names and Identifiers
Isomeric SMILES CCCCCCCCC1=CC=C(C=C1)CCC(CO)(CO)N.Cl
WGK Germany 3
Molecular Weight 343.93
Reaxy-Rn 7837310
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7837310&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Melt Point(°C)110 °C
Documents & Articles
Citations of This Product
References
1. Ziqi Zhou, Yan Zhang, Simin Xia, Xi Chen.  (2023)  Red-Light-Activatable AND-Gated Antitumor Immunosuppressant.  Cells,  12  (19): (2351).  [PMID:37830565] [10.3390/cells12192351]
2. Fan Yang, Dongju Zhao, Meng Cheng, Yining Liu, Ziyao Chen, Jin Chang, Yan Dou.  (2023)  mTOR-Mediated Immunometabolic Reprogramming Nanomodulators Enable Sensitive Switching of Energy Deprivation-Induced Microglial Polarization for Alzheimer’s Disease Management.  ACS Nano,      [PMID:37565731] [10.1021/acsnano.3c03232]
3. Zhou Songlei, Huang Yukun, Chen Yu, Liu Yipu, Xie Laozhi, You Yang, Tong Shiqiang, Xu Jianpei, Jiang Gan, Song Qingxiang, Mei Ni, Ma Fenfen, Gao Xiaoling, Chen Hongzhuan, Chen Jun.  (2023)  Reprogramming systemic and local immune function to empower immunotherapy against glioblastoma.  Nature Communications,  14  (1): (1-20).  [PMID:36702831] [10.1038/s41467-023-35957-8]
4. Yan-Jia Che, Xiao-He Ren, Zhi-Wei Wang, Qi Wu, Kai Xing, Min Zhang, Chang Xu, Di Han, Shun Yuan, Si-Hao Zheng, Yuan-Yang Chen, Xin-Ru Liao, Feng Shi, Xiao-Han Zhong, Xin Cai, Si-Xue Cheng.  (2022)  Lymph-Node-Targeted Drug Delivery for Effective Immunomodulation to Prolong the Long-Term Survival After Heart Transplantation.  ADVANCED MATERIALS,  35  (16): (2207227).  [PMID:36314402] [10.1002/adma.202207227]
5. Taiying Chen, Ngalei Tam, Yu Mao, Chengjun Sun, Zekang Wang, Yuchen Hou, Wuzheng Xia, Jia Yu, Linwei Wu.  (2022)  A multi-hit therapeutic nanoplatform for hepatocellular carcinoma: Dual stimuli-responsive drug release, dual-modal imaging, and in situ oxygen supply to enhance synergistic therapy.  Materials Today Bio,      [PMID:35847375] [10.1016/j.mtbio.2022.100338]
6. Jing Xu, Chang He, Yongsong Cai, Xipeng Wang, Jidong Yan, Jing Zhang, Fujun Zhang, Vilma Urbonaviciute, Yuanyuan Cheng, Shemin Lu, Rikard Holmdahl.  (2024)  NCF4 regulates antigen presentation of cysteine peptides by intracellular oxidative response and restricts activation of autoreactive and arthritogenic T cells.  Redox Biology,      [PMID:38547647] [10.1016/j.redox.2024.103132]
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