Toremifene (Synonyms: Z-Toremifene; NK 622 free base; FC-1157a free base)

Name: Toremifene
Brand: MedChemExpress
SKU: HY-B0005A
Rating: 5.0 (7 reviews)

Cat. No.: HY-B0005A Purity: 99.73%: Data Sheet
COA

SDS
Handling Instructions
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Technical Support

Toremifene (Z-Toremifene) is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis. Toremifene also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC₅₀ of 0.07 µM and 2.6 µM, respectively.

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Toremifene 화학구조

CAS No. : 89778-26-7

사이즈	재고	수량
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO ready for reconstitution	해외재고보유	Estimated Time of Arrival: December 31
Solution
10 mM * 1 mL in DMSO	해외재고보유	Estimated Time of Arrival: December 31
Solid
10 mg	해외재고보유	Estimated Time of Arrival: December 31
25 mg	해외재고보유	Estimated Time of Arrival: December 31
50 mg	견적 받기
100 mg	견적 받기

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고객리뷰

Based on 7 publication(s) in Google Scholar

Other Forms of Toremifene:

7 Publications Citing Use of MCE Toremifene

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View All Isoforms

Estrogen receptor ERα ERβ ERRα ERRβ ERRγ

Biological Activity
순도&문서
References
고객리뷰

제품 설명

Cellular Effect

Cell Line	Type	Value	Description	References
A549	EC₅₀	0.09 μM Compound: toremifene	Inhibition of pseudotyped HIV/EBOV GP infected in human A549 cells assessed as reduction in virus entry measured after 48 hrs by luciferase reporter gene assay Inhibition of pseudotyped HIV/EBOV GP infected in human A549 cells assessed as reduction in virus entry measured after 48 hrs by luciferase reporter gene assay	[PMID: 32490678]
HEK-293T	CC₅₀	17 μM Compound: Tor	Cytotoxicity against HEK293T cells assessed as reduction in cell viability measured after 48 hrs by MTT assay Cytotoxicity against HEK293T cells assessed as reduction in cell viability measured after 48 hrs by MTT assay	[PMID: 38889610]
HEK-293T	EC₅₀	62.8 nM Compound: toremifene	Inhibition of HIV/EBOV GP T519V mutant infected in 293T cells assessed as reduction in virus entry Inhibition of HIV/EBOV GP T519V mutant infected in 293T cells assessed as reduction in virus entry	[PMID: 32490678]
HEK-293T	EC₅₀	62.8 nM Compound: toremifene	Inhibition of HIV/EBOV GP Y517S mutant infected in 293T cells assessed as reduction in virus entry Inhibition of HIV/EBOV GP Y517S mutant infected in 293T cells assessed as reduction in virus entry	[PMID: 32490678]
HeLa	CC₅₀	> 100 μM Compound: Toremifene	Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 24 hrs by MTS assay Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 24 hrs by MTS assay	[PMID: 37021830]
HeLa	EC₅₀	0.67 μM Compound: toremifene	Antiviral activity against Ebola virus 1976 Mayinga infected in human HeLa cells pretreated for 1 hr followed by virus infection measured after 24 hrs by Hoechst staining-based immunofluorescence assay Antiviral activity against Ebola virus 1976 Mayinga infected in human HeLa cells pretreated for 1 hr followed by virus infection measured after 24 hrs by Hoechst staining-based immunofluorescence assay	[PMID: 32490678]
HeLa	EC₅₀	3.25 μM Compound: toremifene	Antiviral activity against Marburg virus Lake Victoria, 2005 Angola infected in human HeLa cells pretreated for 1 hr followed by virus infection measured after 24 hrs by Hoechst staining-based immunofluorescence assay Antiviral activity against Marburg virus Lake Victoria, 2005 Angola infected in human HeLa cells pretreated for 1 hr followed by virus infection measured after 24 hrs by Hoechst staining-based immunofluorescence assay	[PMID: 32490678]
Huh-7	CC₅₀	9.31 μM Compound: 9	Cytotoxicity against human Huh-7 cells assessed as reduction in cell viability by cellular ATP method Cytotoxicity against human Huh-7 cells assessed as reduction in cell viability by cellular ATP method	[PMID: 35872393]
MCF-10A	IC₅₀	> 100 μM Compound: Toremifene	Cytotoxicity against human MCF10A cells by MTT assay Cytotoxicity against human MCF10A cells by MTT assay	[PMID: 31546197]
MCF7	IC₅₀	7 μM Compound: Toremifene	Antiproliferative activity against human MCF7 cells by MTT assay Antiproliferative activity against human MCF7 cells by MTT assay	[PMID: 31546197]
MDA-MB-231	IC₅₀	13 μM Compound: Toremifene	Antiproliferative activity against human MDA-MB-231 cells by MTT assay Antiproliferative activity against human MDA-MB-231 cells by MTT assay	[PMID: 31546197]
Vero	CC₅₀	10.11 μM Compound: Toremiphene	Cell viability measured by CellTiter-Glo assay in Vero cells at MOI 0.05 after 72hr Cell viability measured by CellTiter-Glo assay in Vero cells at MOI 0.05 after 72hr	10.1101/2020.03.20.999730
Vero	IC₅₀	3.58 μM Compound: Toremiphene	Antiviral activity against SARS-CoV-2 (viral titer) measured by plaque assay in Vero cells at MOI 0.0125 after 24 hr Antiviral activity against SARS-CoV-2 (viral titer) measured by plaque assay in Vero cells at MOI 0.0125 after 24 hr	10.1101/2020.03.20.999730
Vero C1008	IC₅₀	0.162 μM Compound: Toremifene	Antiviral activity against Ebolavirus infected in african green monkey Vero E6 cells assessed as reduction in virus entry after 48 hrs by by Celltiter-Glo luminescent assay Antiviral activity against Ebolavirus infected in african green monkey Vero E6 cells assessed as reduction in virus entry after 48 hrs by by Celltiter-Glo luminescent assay	[PMID: 29272110]
Vero C1008	IC₅₀	0.162 μM Compound: Toremifene	Antiviral activity against Ebolavirus expressing eGFP infected in African green monkey Vero E6 cells assessed as inhibition of viral replication after 48 hrs by spectrofluorometric method Antiviral activity against Ebolavirus expressing eGFP infected in African green monkey Vero E6 cells assessed as inhibition of viral replication after 48 hrs by spectrofluorometric method	[PMID: 29741894]

In Vitro

Toremifene is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis and other adverse effects resulting from ADT with prostate cancer^[1].
The growth of Ac-1 cells was inhibited by tamoxifen, toremifene and atamestane in vitro with IC50values of 1.8±1.3μM, 1±0.3μM and 60.4±17.2μM, respectively. The combination of toremifene plusatamestane was found to be better than toremifene or atamestane alone in vitro^[3].

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

In Vivo

The effect of this combination was then studied in vivo using Ac-1 xenografts grown in ovariectomized female SCID mice. The mice were injected with toremifene (1000μg/day), atamestane (1000μg/day), tamoxifen (100μg/day), or the combination of toremifene plus atamestane. In this study, our results indicate that the combination of toremifene plus atamestane was as effective as toremifene or tamoxifen alone but may not provide any additional benefit over toremifene alone or tamoxifen alone^[3].

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

분자량

405.96

화학식

C₂₆H₂₈ClNO

CAS No.

89778-26-7

Appearance

Solid

Color

White to light yellow

SMILES

ClCC/C(C1=CC=CC=C1)=C(C2=CC=C(OCCN(C)C)C=C2)\C3=CC=CC=C3

선적

Room temperature in continental US; may vary elsewhere.

보관

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	6 months
	-20°C	1 month

용액&용해도

In Vitro:

DMSO : 50 mg/mL (123.16 mM; ultrasonic and warming and heat to 60°C; 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	2.4633 mL	12.3165 mL	24.6330 mL
5 mM	0.4927 mL	2.4633 mL	4.9266 mL
10 mM	0.2463 mL	1.2316 mL	2.4633 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)

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

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

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In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

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Working solution concentration: mg/mL

순도&문서

Purity: 99.73%

Select Batch:

Data Sheet (274 KB) SDS (585 KB)

COA (247 KB) HNMR (255 KB) LCMS (103 KB)

Handling Instructions (2659 KB)

References

[1]. Matthew R Smith, Selective Estrogen Receptor Modulators to Prevent Treatment-Related Osteoporosis.Rev Urol. 2005; 7(Suppl 3): S30-S35.

[2]. Laura Cooper, et al. Screening and Reverse-Engineering of Estrogen Receptor Ligands as Potent Pan-Filovirus Inhibitors. J Med Chem. 2020 Sep 4. [Content Brief]

[3]. Gauri J Sabnis, Luciana Macedo, Olga Goloubeva, Toremifene - Atamestane; Alone or In Combination: Predictions from the Preclinical Intratumoral Aromatase Model. J Steroid Biochem Mol Biol. 2008 January; 108(1-2): 1-7.

[4]. Taneja SS, Morton R, Barnette G, Prostate cancer diagnosis among men with isolated high-grade intraepithelial neoplasia enrolled onto a 3-year prospective phase III clinical trial of oral toremifene. J Clin Oncol. 2013 Feb 10;31(5):523-9. [Content Brief]

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	2.4633 mL	12.3165 mL	24.6330 mL	61.5824 mL
	5 mM	0.4927 mL	2.4633 mL	4.9266 mL	12.3165 mL
	10 mM	0.2463 mL	1.2316 mL	2.4633 mL	6.1582 mL
	15 mM	0.1642 mL	0.8211 mL	1.6422 mL	4.1055 mL
	20 mM	0.1232 mL	0.6158 mL	1.2316 mL	3.0791 mL
	25 mM	0.0985 mL	0.4927 mL	0.9853 mL	2.4633 mL
	30 mM	0.0821 mL	0.4105 mL	0.8211 mL	2.0527 mL
	40 mM	0.0616 mL	0.3079 mL	0.6158 mL	1.5396 mL
	50 mM	0.0493 mL	0.2463 mL	0.4927 mL	1.2316 mL
	60 mM	0.0411 mL	0.2053 mL	0.4105 mL	1.0264 mL
	80 mM	0.0308 mL	0.1540 mL	0.3079 mL	0.7698 mL
	100 mM	0.0246 mL	0.1232 mL	0.2463 mL	0.6158 mL

Toremifene Related Classifications

Infection Cancer

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.

Keywords:

Toremifene89778-26-7Z-ToremifeneNK 622FC-1157aNK622NK-622Estrogen Receptor/ERRInhibitorinhibitorinhibit

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Toremifene (Synonyms: Z-Toremifene; NK 622 free base; FC-1157a free base)

고객리뷰

Other Forms of Toremifene:

Toremifene Related Antibodies

7 Publications Citing Use of MCE Toremifene

Featured Recommendations

•Related Screening Libraries:

•Related Small Molecules:

•Related Proteins:

View All Estrogen Receptor/ERR Isoform Specific Products:

Biological Activity

순도&문서

References

고객리뷰

Toremifene Related Antibodies

몰농도 계산기

농도 희석 계산기

Complete Stock Solution Preparation Table

Toremifene Related Classifications

Keywords:

최근 본 상품:

고객리뷰

Request for HNMR Report

SAFETY DATA SHEET (SDS)

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