Menaquinone-7 - Vitamin K2 Subtype - MedChemExpress

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                                4. Menaquinone-7
                                Menaquinone-7 (Synonyms: Vitamin K2-7; Vitamin K2(35); Vitamin MK-7) Cat. No.: HY-112499 Purity: 98.51% Data Sheet COA SDS Handling Instructions FAQs Technical Support

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                                Menaquinone-7 (Vitamin K2-7), belongs to a class of K2-vitamin homologs (orally active), is originally discovered as the anti-hemorrhagic factors. Menaquinone-7 inhibits osteoclast bone resorption in vitro and stimulates bone formation in femoral tissue of aged female rats. Menaquinone-7 has a well-researched potential in the prevention of aging-induced bone degeneration. Menaquinone-7 is also a pharmacological option for activating Gla matrix protein and intervening in the progression of calcific aortic stenosis (CAVS).

                                For research use only. We do not sell to patients.

                                Menaquinone-7

                                Menaquinone-7 Chemical Structure

                                CAS No. : 2124-57-4

                                Size Price Stock Quantity
                                5 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                10 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                50 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                100 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
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                                Based on 3 publication(s) in Google Scholar

                                Other Forms of Menaquinone-7:

                                • Menaquinone-7-13C6 In-stock
                                • Menaquinone-7 (Standard) In-stock
                                • Menaquinone-7-d7 Get quote

                                Menaquinone-7 Related Antibodies

                                Top Publications Citing Use of Products

                                3 Publications Citing Use of MCE Menaquinone-7

                                • Biomed Pharmacother. 2024 May 16:175:116697. [Abstract]
                                • Int J Antimicrob Agents. 2025 Nov 25;67(1):107679. [Abstract]
                                • J Sci Food Agric. 2025 Aug 30;105(11):5973-5985. [Abstract]
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                                Related Small Molecules:

                                Related Proteins:

                                • Biological Activity

                                • Purity & Documentation

                                • References

                                • Customer Review

                                Description

                                Menaquinone-7 (Vitamin K2-7), belongs to a class of K2-vitamin homologs (orally active), is originally discovered as the anti-hemorrhagic factors. Menaquinone-7 inhibits osteoclast bone resorption in vitro and stimulates bone formation in femoral tissue of aged female rats. Menaquinone-7 has a well-researched potential in the prevention of aging-induced bone degeneration. Menaquinone-7 is also a pharmacological option for activating Gla matrix protein and intervening in the progression of calcific aortic stenosis (CAVS)[1][2][3][4][5].

                                In Vitro

                                Menaquinone-7 (0.01-10 μM; 7 days) inhibits osteoclast-like cell formation in marrow cultures[1]. Menaquinone-7 (10 μM) promotes the expression of tenascin C and increases phosphorylated Smad1 level in MC3T3E1 cells[2]. Menaquinone-7 (1, 10 μM) significantly enhances the anabolic effect on the femoral calcium content in the presence of phytoestrogen genistein (1, 10 μM)[3].

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

                                Menaquinone-7 Related Antibodies

                                Cell Viability Assay[1]

                                Cell Line: Marrow cells (from 3-week-old male wistar rats; PTH/PGE2 stimulated)
                                Concentration: 0.01-10 µM
                                Incubation Time: 7 days
                                Result: Significantly decreased the number of TRACP-positive MNCs stimulated by PTH or PGE2.
                                In Vivo

                                Menaquinone-7 (18.1 mg/100 g diet; in animal feedings; 24 days) shows a preventive effect on bone loss in ovariectomized rats[5].

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

                                Animal Model: Female Wistar rats (5-week-old; ovariectomized (OVX) rats model)[5].
                                Dosage: 18.1 mg/100 g diet
                                Administration: In animal feedings; 24 days
                                Result: Had a preventive effect on OVX-induced bone loss.
                                Clinical Trial
                                Molecular Weight

                                649.00

                                Formula

                                C46H64O2

                                CAS No.

                                2124-57-4

                                Appearance

                                Solid

                                Color

                                Light yellow to yellow

                                SMILES

                                O=C1C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)\C)=C(C)C(C2=C1C=CC=C2)=O

                                Shipping

                                Room temperature in continental US; may vary elsewhere.

                                Storage
                                Powder -20°C 3 years
                                4°C 2 years
                                In solvent -80°C 2 years
                                -20°C 1 year
                                Solvent & Solubility In Vitro:

                                Ethanol : 10 mg/mL (15.41 mM; Need ultrasonic)

                                DMSO : 5 mg/mL (7.70 mM; Need ultrasonic and warming; 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 1.5408 mL 7.7042 mL 15.4083 mL
                                5 mM 0.3082 mL 1.5408 mL 3.0817 mL
                                10 mM 0.1541 mL 0.7704 mL 1.5408 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

                                • Molarity Calculator

                                • Dilution Calculator

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

                                Mass kg g mg μg ng pg = Concentration M mM μM nM pM × Volume L mL μL × Molecular Weight *

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

                                This equation is commonly abbreviated as: C1V1 = C2V2

                                Concentration (start) M mM μM nM pM

                                C1

                                × Volume (start) L mL μL

                                V1

                                = Concentration (final) M mM μM nM pM

                                C2

                                × Volume (final) L mL μL

                                V2

                                In Vivo:

                                Select the appropriate dissolution method based on your experimental animal and administration route.

                                For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents: To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day. The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

                                • Protocol 1

                                  Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

                                  Solubility: 0.54 mg/mL (0.83 mM); Suspended solution; Need ultrasonic

                                  This protocol yields a suspended solution of 0.54 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

                                  Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (5.4 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

                                  Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
                                • Protocol 2

                                  Add each solvent one by one: 10% DMSO 90% Corn Oil

                                  Solubility: ≥ 0.54 mg/mL (0.83 mM); Clear solution

                                  This protocol yields a clear solution of ≥ 0.54 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

                                  Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (5.4 mg/mL) to 900 μL Corn oil, and mix evenly.

                                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. Please enter your animal formula composition: % DMSO + % + % Tween-80 + % Saline Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak. The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE). Calculation results: Working solution concentration: mg/mL Method for preparing stock solution: mg drug dissolved in μL DMSO (Stock solution concentration: mg/mL). The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE). Tel: 609-228-6898 E-mail: [email protected] Technical Support: [email protected] Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline. Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution If the continuous dosing period exceeds half a month, please choose this protocol carefully. Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
                                Purity & Documentation

                                Purity: 98.51%

                                Select Batch: HY-112499-988481 HY-112499-38644 HY-112499-673198 HY-112499-656247 HY-112499-38756 HY-112499-107899 Data Sheet (272 KB) SDS (393 KB)

                                COA (239 KB) HNMR (301 KB) RP-HPLC (243 KB) MS (85 KB)

                                Handling Instructions (2659 KB)
                                References
                                • [1]. Yamaguchi M, et al. Inhibitory effect of menaquinone-7 (vitamin K2) on osteoclast-like cell formation and osteoclastic bone resorption in rat bone tissues in vitro. Mol Cell Biochem. 2001 Dec;228(1-2):39-47. [Content Brief]

                                  [2]. Katsuyama H, et al. Menaquinone-7 regulates gene expression in osteoblastic MC3T3E1 cells. Int J Mol Med. 2007 Feb;19(2):279-84. [Content Brief]

                                  [3]. Yamaguchi M, et al. Stimulatory effect of menaquinone-7 on bone formation in elderly female rat femoral tissues in vitro: prevention of bone deterioration with aging. Int J Mol Med. 2002 Dec;10(6):729-33. [Content Brief]

                                  [4]. Peeters FECM, et al. Bicuspid Aortic Valve Stenosis and the Effect of Vitamin K2 on Calcification Using 18F-Sodium Fluoride Positron Emission Tomography/Magnetic Resonance: The BASIK2 Rationale and Trial Design. Nutrients. 2018 Mar 21;10(4):386. [Content Brief]

                                  [5]. Yamaguchi M, Taguchi H, Gao YH, Igarashi A, Tsukamoto Y. Effect of vitamin K2 (menaquinone-7) in fermented soybean (natto) on bone loss in ovariectomized rats. J Bone Miner Metab. 1999;17(1):23-9. [Content Brief]

                                • [1]. Yamaguchi M, et al. Inhibitory effect of menaquinone-7 (vitamin K2) on osteoclast-like cell formation and osteoclastic bone resorption in rat bone tissues in vitro. Mol Cell Biochem. 2001 Dec;228(1-2):39-47.

                                  [2]. Katsuyama H, et al. Menaquinone-7 regulates gene expression in osteoblastic MC3T3E1 cells. Int J Mol Med. 2007 Feb;19(2):279-84.

                                  [3]. Yamaguchi M, et al. Stimulatory effect of menaquinone-7 on bone formation in elderly female rat femoral tissues in vitro: prevention of bone deterioration with aging. Int J Mol Med. 2002 Dec;10(6):729-33.

                                  [4]. Peeters FECM, et al. Bicuspid Aortic Valve Stenosis and the Effect of Vitamin K2 on Calcification Using 18F-Sodium Fluoride Positron Emission Tomography/Magnetic Resonance: The BASIK2 Rationale and Trial Design. Nutrients. 2018 Mar 21;10(4):386.

                                  [5]. Yamaguchi M, Taguchi H, Gao YH, Igarashi A, Tsukamoto Y. Effect of vitamin K2 (menaquinone-7) in fermented soybean (natto) on bone loss in ovariectomized rats. J Bone Miner Metab. 1999;17(1):23-9.

                                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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

                                Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
                                DMSO / Ethanol 1 mM 1.5408 mL 7.7042 mL 15.4083 mL 38.5208 mL
                                5 mM 0.3082 mL 1.5408 mL 3.0817 mL 7.7042 mL
                                Ethanol 10 mM 0.1541 mL 0.7704 mL 1.5408 mL 3.8521 mL
                                15 mM 0.1027 mL 0.5136 mL 1.0272 mL 2.5681 mL
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                                Menaquinone-7 Related Classifications

                                • Disease Areas
                                • Blood or Cardiovascular Disease
                                • Cardiovascular Disease
                                • Cardiovascular Disease
                                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:

                                Menaquinone-72124-57-4Vitamin K2-7 Vitamin K2(35) Vitamin MK-7Menaquinone7Menaquinone 7Vitamin MK7Vitamin MK 7Vitamin MK-7OthersCAVSmarrow cellMC3T3E1 cellsosteoporosisanti-hemorrhagicInhibitorinhibitorinhibit

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