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Minocycline HCl

Catalog No.GC11861

Minocycline HCl은 구강 내 복용이 가능하고 혈뇨 장벽을 통과할 수 있는 반합성 테트라사이클린 항생제이다.

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Minocycline HCl Chemical Structure

Cas No.: 13614-98-7

Size 가격 재고 수량
50mg
US$35.00
재고 있음
100mg
US$45.00
재고 있음

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고객 리뷰

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

Product has been cited by 4 publications

Description of Minocycline HCl

Minocycline HCl은 구강 내 복용이 가능하고 혈뇨 장벽을 통과할 수 있는 반합성 테트라사이클린 항생제이다. Minocycline HCl은 낮은 산소 유도 인자 (HIF-1α) 억제제로 항암, 항염증 및 글루타마테 반작용 효과 그리고 신경 보호 및 항우울 성질을 가지고 있다[2]. Minocycline HCl은 박테리아 리보솜 30S 서브 유닛과 결합하여 박테리아 단백질 합성을 억제함으로써 항균 효과를 발휘한다[3].

체외 실험에서 Minocycline HCl(10μM)를 SH-SY5Y 세포에 24시간 동안 처리하여 6-히드록시도파민(6-OHDA)에 의한 세포 사망을 현저하게 억제하고 세포 DNA 조각화와 염색질 응축을 억제했다[4]. Minocycline HCl(0-100μM)를 유방암 세포 라인(OVCAR-3, SKOV-3, A2780 세포)에 24-72시간 동안 처리하여 세포 증식과 균락 형성을 억제하고 세포라인 단백질 A, B, E의 표현을 하강시키고 DNA 합성을 억제하고 DNA 사다리, 시스테인-3 활성화 및 PARP-1 절단을 유도했다[5].

체내 실험에서 복강 주사로 Minocycline HCl(25, 50mg/kg)를 척수손상 모델 쥐에 28일 동안 치료하고 축엽의 무결성을 현저하게 보호하고 조직 손실을 예방하고 운동 행동을 개선했다[6]. Minocycline HCl(3, 10mg/kg)를 일시성 중뇌동맥 차단(TMCAO)모델인 쥐의 목정맥에 주입하고 뇌경색 면적을 효과적으로 줄이고 신경 기능 결함을 현저하게 개선했다[7].

References:
[1] Zhou J, Yang J, Dai M, et al. A combination of inhibiting microglia activity and remodeling gut microenvironment suppresses the development and progression of experimental autoimmune uveitis[J]. Biochemical Pharmacology, 2020, 180: 114108.
[2] Pajarillo E, Nyarko-Danquah I, Digman A, et al. Mechanisms of manganese-induced neurotoxicity and the pursuit of neurotherapeutic strategies[J]. Frontiers in Pharmacology, 2022, 13: 1011947.
[3] Singh S, Khanna D, Kalra S. Minocycline and doxycycline: more than antibiotics[J]. Current Molecular Pharmacology, 2021, 14(6): 1046-1065.
[4] Ossola B, Lantto T A, Puttonen K A, et al. Minocycline protects SH‐SY5Y cells from 6‐hydroxydopamine by inhibiting both caspase‐dependent and‐independent programmed cell death[J]. Journal of neuroscience research, 2012, 90(3): 682-690.
[5] Pourgholami M H, Mekkawy A H, Badar S, et al. Minocycline inhibits growth of epithelial ovarian cancer[J]. Gynecologic oncology, 2012, 125(2): 433-440.
[6] Wells J E A, Hurlbert R J, Fehlings M G, et al. Neuroprotection by minocycline facilitates significant recovery from spinal cord injury in mice[J]. Brain, 2003, 126(7): 1628-1637.
[7] Xu L, Fagan S C, Waller J L, et al. Low dose intravenous minocycline is neuroprotective after middle cerebral artery occlusion-reperfusion in rats[J]. BMC neurology, 2004, 4: 1-7.

Protocol of Minocycline HCl

세포 실험 [1]:

세포 라인

SH-SY5Y 세포

제조 방법

SH-SY5Y 세포는 신경 독소에 24시간과 48시간 동안 노출하기 전에 다양한 농도의 Minocycline HCl(1, 10, 50μM)로 24시간 동안 사전 재배되었습니다.

반응 조건

1, 10, 50μM; 24시간 동안

응용 분야

Minocycline HCl은 6-히드록시도파민(6-OHDA)에 의한 세포 사망을 현저하게 방지했고 약물 농도가 10μM일 때 현저한 보호 효과를 관찰했습니다.

동물 실험 [2]:

동물 모형

수컷 CD‐1 쥐

제조 방법

쥐에게는 복강 주사로 식염수 또는 50mg/kg Minocycline HCl을 투여했습니다. 그 후 24시간 후에 50mg/kg의 두 번째 주사를 받았습니다. 치료받은 쥐는 다음 5일 동안 매일 25mg/kg의 용량을 주사 받았습니다. 모든 동물은 척수손상(SCI) 후 28일째에 사망되었습니다.

제형

25、50mg/kg; i.p.

응용 분야

SCI 모델의 쥐에서 Minocycline HCl은 축엽의 무결성을 현저하게 보호하고 조직 손실을 예방하고 운동 행동 개선을 이끌어냈습니다.

References:
[1] Ossola B, Lantto T A, Puttonen K A, et al. Minocycline protects SH?SY5Y cells from 6?hydroxydopamine by inhibiting both caspase?dependent and?independent programmed cell death[J]. Journal of neuroscience research, 2012, 90(3): 682-690.
[2]Wells J E A, Hurlbert R J, Fehlings M G, et al. Neuroprotection by minocycline facilitates significant recovery from spinal cord injury in mice[J]. Brain, 2003, 126(7): 1628-1637.

Chemical Properties of Minocycline HCl

Cas No. 13614-98-7 SDF
Chemical Name (4S,4aS,5aR,12aR)-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4H-tetracene-2-carboxamide;hydrochloride
Canonical SMILES CN(C)C1C2CC3CC4=C(C=CC(=C4C(=C3C(=O)C2(C(=C(C1=O)C(=O)N)O)O)O)O)N(C)C.Cl
Formula C23H28ClN3O7 M.Wt 493.94
Solubility ≥ 60.7 mg/mL in DMSO with gentle warming, ≥ 7.86 mg/mL in Water with gentle warming Storage Store at 2-8°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 Minocycline HCl

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.0245 mL 10.1227 mL 20.2454 mL
5 mM 404.9 μL 2.0245 mL 4.0491 mL
10 mM 202.5 μL 1.0123 mL 2.0245 mL
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In vivo Formulation Calculator (Clear solution) of Minocycline HCl

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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.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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3. All of the above co-solvents are available for purchase on the GlpBio website.

Product Documents

Quality Control & SDS

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Quality Control

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    Minocycline HCl-GlpBio

리뷰

Review for Minocycline HCl

Average Rating: 5 ★★★★★ (Based on Reviews and 18 reference(s) in Google Scholar.)

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