>>Signaling Pathways>> Proteases>> MMP>>MMP-2/MMP-9 Inhibitor I

MMP-2/MMP-9 Inhibitor I (Synonyms: Metalloproteinase-2/Metalloproteinase-9 Inhibitor I)

Catalog No.GC11038 Copy One-Click Copy Product Info

MMP-2/MMP-9 억제제 I은 IC50이 각각 0.24 및 0.31 μ이고 MMP-9 및 MMP-2에 대해 M인 고도로 선택적이고 경구 활성이며 강력한 IV형 콜라게나제(MMP-9 및 MMP-2) 억제제입니다. . MMP-2/MMP-9 억제제 I은 종양 성장 및 전이 동물 모델에서 경구 활성입니다. MMP-2/MMP-9 억제제 I는 암 연구에 사용할 수 있습니다.

Products are for research use only. Not for human use. We do not sell to patients.

MMP-2/MMP-9 Inhibitor I Chemical Structure

Cas No.: 193807-58-8

Size 가격 재고 수량
10mM (in 1mL DMSO)
US$123.00
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5mg
US$112.00
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10mg
US$168.00
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25mg
US$343.00
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고객 리뷰

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.



Description of MMP-2/MMP-9 Inhibitor I

IC50: 310 and 240 nM for MMP-2 and MMP-9, respectively

MMP-2/MMP-9 Inhibitor I is a potent inhibitor of matrix metalloproteinase-2 (MMP-2) and MMP-9.

Matrix metalloproteinase (MMP), a typical metalloproteinase, requires zinc ion at its active sites. As many as 18 kinds of MMP have been identified and cloned and are collectively called the MMP family.

In vitro: MMP-2/MMP-9 inhibitor I was identified as a potent inhibitor of matrix metalloproteinase-2 (MMP-2) and MMP-9 with IC50 values of 310 and 240 nM, respectively. MMP-2/MMP-9 inhibitor I acted by binding zinc at the active site of these MMPs. MMP-2/MMP-9 inhibitor I was found to be able to block MMP-2/MMP-9-dependent invasion in cell culture model [1].

In vivo: Both hydroxamic acid and carboxylic acid analogs of MMP-2/MMP-9 inhibitor I were evaluated for their inhibitory activities in animal cancer models. Results showed that lung colonization of Lewis lung carcinoma cells was suppressed by these inhibitors significantly. In addition, antitumor activity was also observed in the human lung cancer model. Ma44 cells growed as a solid tumor on the peritoneum after being implanted ip, and mice bearing Ma44 eventually died within 3 to 4 weeks. Daily oral administration of compound 5l led to prolonged survival of Ma44-bearing mice [1].

Clinical trial: So far, no clinical study has been conducted.

Reference:
[1] Tamura, Y. ,Watamane, F.,Nakatani, T., et al. Highly selective and orally active inhibitors of type IV collagenase (MMP-9 and MMP-2): N-sulfonylamino acid derivatives. J. Med. Chem. 41(4), 640-649 (1998).

Chemical Properties of MMP-2/MMP-9 Inhibitor I

Cas No. 193807-58-8 SDF
Synonyms Metalloproteinase-2/Metalloproteinase-9 Inhibitor I
Chemical Name N-([1,1'-biphenyl]-4-ylsulfonyl)-D-phenylalanine
Canonical SMILES O=S(C(C=C1)=CC=C1C2=CC=CC=C2)(N[C@@H](C(O)=O)CC3=CC=CC=C3)=O
Formula C21H19NO4S M.Wt 381.4
Solubility ≤25mM in DMSO Storage Store at 4°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of MMP-2/MMP-9 Inhibitor I

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1 mg 5 mg 10 mg
1 mM 2.6219 mL 13.1096 mL 26.2192 mL
5 mM 524.4 μL 2.6219 mL 5.2438 mL
10 mM 262.2 μL 1.311 mL 2.6219 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Review for MMP-2/MMP-9 Inhibitor I

Average Rating: 5 ★★★★★ (Based on Reviews and 6 reference(s) in Google Scholar.)

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