1. Membrane Transporter/Ion Channel
  2. Monoamine Transporter Sodium Channel
  3. Nisoxetine

Nisoxetine is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. Nisoxetine is an antidepressant and local anesthetic, it can block voltage-gated sodium channels.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

Nisoxetine

Nisoxetine 화학구조

CAS No. : 53179-07-0

사이즈 가격 재고 수량
Solid or liquid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
해외재고보유
Solution
10 mM * 1 mL in DMSO 해외재고보유
Solid or liquid
5 mg 해외재고보유
10 mg 해외재고보유
25 mg 해외재고보유
50 mg 해외재고보유
100 mg 해외재고보유
200 mg   견적 받기  
500 mg   견적 받기  

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

This product is a controlled substance and not for sale in your territory.

고객리뷰

Based on 1 publication(s) in Google Scholar

Other Forms of Nisoxetine:

Top Publications Citing Use of Products

1 Publications Citing Use of MCE Nisoxetine

  • Biological Activity

  • 순도&문서

  • References

  • 고객리뷰

제품 설명

Nisoxetine is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. Nisoxetine is an antidepressant and local anesthetic, it can block voltage-gated sodium channels[1][2][3].

IC50 & Target

Kd: 0.76 nM (NET)[1]

Cellular Effect
Cell Line Type Value Description References
MDCK IC50
6 1
Compound: 5
Inhibition of norepinephrine uptake at human NET expressed in MDCK cells
Inhibition of norepinephrine uptake at human NET expressed in MDCK cells
[PMID: 18771916]
HEK293 IC50
1150 1
Compound: nisoxetine
Inhibition of human DAT expressed in HEK293 cells assessed as inhibition of dopamine reuptake after 30 mins by fluorescence assay
Inhibition of human DAT expressed in HEK293 cells assessed as inhibition of dopamine reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
1150 1
Compound: Nisoxetine
Inhibition of human DAT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human DAT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
MDCK IC50
8.3 1
Compound: Nisoxetine
Inhibition of [3H]norepinephrine reuptake at human NET expressed in MDCK cells by scintillation counting
Inhibition of [3H]norepinephrine reuptake at human NET expressed in MDCK cells by scintillation counting
[PMID: 21093273]
HEK293 IC50
1150 1
Compound: Nisoxetine
Inhibition of DA reuptake at human DAT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of DA reuptake at human DAT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
1150 1
Compound: Nisoxetine
Inhibition of DA reuptake at human DAT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of DA reuptake at human DAT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
15 1
Compound: Nisoxetine
Inhibition of norepinephrine uptake at human NET expressed in HEK cells
Inhibition of norepinephrine uptake at human NET expressed in HEK cells
[PMID: 18667309]
HEK293 IC50
1150 1
Compound: Nisoxetine
Inhibition of human DAT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human DAT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
18 1
Compound: nisoxetine
Inhibition of human NET expressed in HEK293 cells assessed as inhibition of noradrenaline reuptake after 30 mins by fluorescence assay
Inhibition of human NET expressed in HEK293 cells assessed as inhibition of noradrenaline reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
15 1
Compound: 2
Inhibition of norepinephrine uptake at human NET in human HEK293 cells
Inhibition of norepinephrine uptake at human NET in human HEK293 cells
[PMID: 18550369]
HEK293 IC50
1150 1
Compound: nisoxetine
Inhibition of human DAT expressed in HEK293 cells assessed as inhibition of dopamine reuptake after 30 mins by fluorescence assay
Inhibition of human DAT expressed in HEK293 cells assessed as inhibition of dopamine reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
18 1
Compound: nisoxetine
Inhibition of human NET expressed in HEK293 cells assessed as inhibition of noradrenaline reuptake after 30 mins by fluorescence assay
Inhibition of human NET expressed in HEK293 cells assessed as inhibition of noradrenaline reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
20 1
Compound: Nisoxetine
Inhibition of human NET expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human NET expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
1400 1
Compound: 2
Inhibition of serotonin uptake at human SERT in human HEK293 cells
Inhibition of serotonin uptake at human SERT in human HEK293 cells
[PMID: 18550369]
HEK293 IC50
20 1
Compound: Nisoxetine
Inhibition of norepinephrine reuptake at human NET expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of norepinephrine reuptake at human NET expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
20 1
Compound: Nisoxetine
Inhibition of human NET expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human NET expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
700 1
Compound: nisoxetine
Inhibition of human SERT expressed in HEK293 cells assessed as inhibition of serotonin reuptake after 30 mins by fluorescence assay
Inhibition of human SERT expressed in HEK293 cells assessed as inhibition of serotonin reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
1400 1
Compound: Nisoxetine
Inhibition of serotonin uptake at human SERT expressed in HEK cells
Inhibition of serotonin uptake at human SERT expressed in HEK cells
[PMID: 18667309]
HEK293 IC50
20 1
Compound: Nisoxetine
Inhibition of norepinephrine reuptake at human NET expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of norepinephrine reuptake at human NET expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
JAR IC50
277 1
Compound: 5
Inhibition of serotonin uptake at human SERT expressed in JAR cells
Inhibition of serotonin uptake at human SERT expressed in JAR cells
[PMID: 18771916]
HEK293 IC50
15 1
Compound: 2
Inhibition of norepinephrine uptake at human NET in human HEK293 cells
Inhibition of norepinephrine uptake at human NET in human HEK293 cells
[PMID: 18550369]
HEK293 IC50
700 1
Compound: Nisoxetine
Inhibition of human SERT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human SERT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
700 1
Compound: Nisoxetine
Inhibition of serotonin reuptake at human SERT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of serotonin reuptake at human SERT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
15 1
Compound: Nisoxetine
Inhibition of norepinephrine uptake at human NET expressed in HEK cells
Inhibition of norepinephrine uptake at human NET expressed in HEK cells
[PMID: 18667309]
HEK293 IC50
700 1
Compound: nisoxetine
Inhibition of human SERT expressed in HEK293 cells assessed as inhibition of serotonin reuptake after 30 mins by fluorescence assay
Inhibition of human SERT expressed in HEK293 cells assessed as inhibition of serotonin reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
18 1
Compound: nisoxetine
Inhibition of human NET expressed in HEK293 cells assessed as inhibition of noradrenaline reuptake after 30 mins by fluorescence assay
Inhibition of human NET expressed in HEK293 cells assessed as inhibition of noradrenaline reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
MDCK IC50
8.3 1
Compound: Nisoxetine
Inhibition of [3H]norepinephrine reuptake at human NET expressed in MDCK cells by scintillation counting
Inhibition of [3H]norepinephrine reuptake at human NET expressed in MDCK cells by scintillation counting
[PMID: 21093273]
HEK293 IC50
700 1
Compound: Nisoxetine
Inhibition of human SERT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human SERT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
20 1
Compound: Nisoxetine
Inhibition of norepinephrine reuptake at human NET expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of norepinephrine reuptake at human NET expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
700 1
Compound: Nisoxetine
Inhibition of serotonin reuptake at human SERT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of serotonin reuptake at human SERT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
20 1
Compound: Nisoxetine
Inhibition of human NET expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human NET expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
1150 1
Compound: Nisoxetine
Inhibition of DA reuptake at human DAT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of DA reuptake at human DAT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
2400 1
Compound: 2
Inhibition of dopamine uptake at human DAT in human HEK293 cells
Inhibition of dopamine uptake at human DAT in human HEK293 cells
[PMID: 18550369]
HEK293 IC50
1150 1
Compound: nisoxetine
Inhibition of human DAT expressed in HEK293 cells assessed as inhibition of dopamine reuptake after 30 mins by fluorescence assay
Inhibition of human DAT expressed in HEK293 cells assessed as inhibition of dopamine reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
1150 1
Compound: Nisoxetine
Inhibition of human DAT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human DAT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
2400 1
Compound: Nisoxetine
Inhibition of dopamine uptake at human DAT expressed in HEK cells
Inhibition of dopamine uptake at human DAT expressed in HEK cells
[PMID: 18667309]
HEK293 IC50
700 1
Compound: Nisoxetine
Inhibition of serotonin reuptake at human SERT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
Inhibition of serotonin reuptake at human SERT expressed in HEK293 cells after 15 mins by fluorescence neurotransmitter transporter assay
[PMID: 24974340]
HEK293 IC50
1400 1
Compound: Nisoxetine
Inhibition of serotonin uptake at human SERT expressed in HEK cells
Inhibition of serotonin uptake at human SERT expressed in HEK cells
[PMID: 18667309]
HEK293 IC50
700 1
Compound: Nisoxetine
Inhibition of human SERT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
Inhibition of human SERT expressed in HEK293 cells at incubated for 15 mins by neurotransmitter reuptake assay
[PMID: 25221656]
HEK293 IC50
1400 1
Compound: 2
Inhibition of serotonin uptake at human SERT in human HEK293 cells
Inhibition of serotonin uptake at human SERT in human HEK293 cells
[PMID: 18550369]
HEK293 IC50
2400 1
Compound: Nisoxetine
Inhibition of dopamine uptake at human DAT expressed in HEK cells
Inhibition of dopamine uptake at human DAT expressed in HEK cells
[PMID: 18667309]
HEK293 IC50
700 1
Compound: nisoxetine
Inhibition of human SERT expressed in HEK293 cells assessed as inhibition of serotonin reuptake after 30 mins by fluorescence assay
Inhibition of human SERT expressed in HEK293 cells assessed as inhibition of serotonin reuptake after 30 mins by fluorescence assay
[PMID: 22938049]
HEK293 IC50
2400 1
Compound: 2
Inhibition of dopamine uptake at human DAT in human HEK293 cells
Inhibition of dopamine uptake at human DAT in human HEK293 cells
[PMID: 18550369]
JAR IC50
277 1
Compound: 5
Inhibition of serotonin uptake at human SERT expressed in JAR cells
Inhibition of serotonin uptake at human SERT expressed in JAR cells
[PMID: 18771916]
MDCK IC50
6 1
Compound: 5
Inhibition of norepinephrine uptake at human NET expressed in MDCK cells
Inhibition of norepinephrine uptake at human NET expressed in MDCK cells
[PMID: 18771916]
MDCK IC50
8.3 1
Compound: Nisoxetine
Inhibition of [3H]norepinephrine reuptake at human NET expressed in MDCK cells by scintillation counting
Inhibition of [3H]norepinephrine reuptake at human NET expressed in MDCK cells by scintillation counting
[PMID: 21093273]
In Vitro

Nisoxetine inhibits [3H]Nisoxetine binding to rat frontal cortical membranes with a Ki of 1.4±0.1 nM[2].
Nisoxetine inhibits [3H]Noradrenaline uptake into rat frontal cortical synaptosomes with a Ki of 2.1±0.3 nM[2].
Nisoxetine inhibits Na+ currents with IC50s of 1.6 and 28.6 μM at the membrane potential of -70 and -100 mV, respectively[3].

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

In Vivo

Nisoxetine (2.2 μM; a single intrathecal injection) shows 100, 100, and 100% of blockades in motor function, proprioception, and with duration of action of about 61, 96, and 236 min, respectively[3].
Nisoxetine (3,10, 30 mg/kg, i.p.) inhibits refeeding response (intake of standard chow) in rats[4].

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

Animal Model: Sprague-Dawley rats(290-340 g)[3]
Dosage: 0.6, 1.2, 1.8, 2.2 µM
Administration: A single intrathecal injection
Result: Showed ED50s of 0.82, 0.75 and 0.70 µM in blocking motor function, proprioception, and nociception respectively.
분자량

271.35

화학식

C17H21NO2

CAS No.
Appearance

Viscous Liquid

Color

Colorless to light yellow

SMILES

CNCCC(OC1=CC=CC=C1OC)C2=CC=CC=C2

선적

Room temperature in continental US; may vary elsewhere.

보관
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
용액&용해도
In Vitro: 

DMSO : 250 mg/mL (921.32 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.6853 mL 18.4264 mL 36.8528 mL
5 mM 0.7371 mL 3.6853 mL 7.3706 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • 몰농도 계산기

  • 농도 희석 계산기

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
순도&문서
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.6853 mL 18.4264 mL 36.8528 mL 92.1319 mL
5 mM 0.7371 mL 3.6853 mL 7.3706 mL 18.4264 mL
10 mM 0.3685 mL 1.8426 mL 3.6853 mL 9.2132 mL
15 mM 0.2457 mL 1.2284 mL 2.4569 mL 6.1421 mL
20 mM 0.1843 mL 0.9213 mL 1.8426 mL 4.6066 mL
25 mM 0.1474 mL 0.7371 mL 1.4741 mL 3.6853 mL
30 mM 0.1228 mL 0.6142 mL 1.2284 mL 3.0711 mL
40 mM 0.0921 mL 0.4607 mL 0.9213 mL 2.3033 mL
50 mM 0.0737 mL 0.3685 mL 0.7371 mL 1.8426 mL
60 mM 0.0614 mL 0.3071 mL 0.6142 mL 1.5355 mL
80 mM 0.0461 mL 0.2303 mL 0.4607 mL 1.1516 mL
100 mM 0.0369 mL 0.1843 mL 0.3685 mL 0.9213 mL
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

최근 본 상품:

온라인 문의

Your information is safe with us. * Required Fields.

상품명

 

Requested Quantity *

고객명 *

 

호칭

메일주소 *

 

전화번호 *

Department

 

회사명 *

City

Country or Region *

     

비고

대량구매 문의

Inquiry Information

상품명:
Nisoxetine
Cat. No.:
HY-B1704
수량:
MCE Japan Authorized Agent: