CBR-470-2 - ≥99% , CAS No.2416095-00-4

CAS: 2416095-00-4 Cat. No.: C650324 분자식: C12H13Cl2NO6S2 분자량: 402.27 PubChem CID: 155819525
주문 가능
등급 & 순도 ≥99%
Storage
Store at 2-8°C
Shipped In
Wet ice
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수량
5mg
C650324-5mg
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US$960.90
10mg
C650324-10mg
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25mg
C650324-25mg
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50mg
C650324-50mg
주문제작 · 8~12주
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100mg
C650324-100mg
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개요

CBR-470-2, a glycine-substituted analog, can activate NRF2 signaling. CBR-470-2 can be used for the research of modulation glycolysis

In Vitro

CBR-470-2 (1-10 μM; 24 h) increases transcript levels of the NRF2-responsive genes NQO1 and HMOX1 in epidermal keratinocytes and dermal fibroblasts. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

CBR-470-2 (50 mg/kg; p.o. twice daily for 10 d) induces activation of NRF2 signaling in vivo . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Balb/C mice (5-week old) are exposed to UVB Dosage: 50 mg/kg Administration: P.o. twice daily for 10 days Result: Resulted in comparable beneficial effects on erythema histological scores and total wounded area. Decreased epidermal thickness in response to UV exposure.

Form:Solid

IC50& Target:NRF2

사양

사양 및 순도
≥99%
생화학 및 생리적 메커니즘
CBR-470-2, a glycine-substituted analog, can activate NRF2 signaling. CBR-470-2 can be used for the research of modulation glycolysis.
보관 조건
Store at 2-8°C
배송
Wet ice
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작업 유형
ACTIVATOR
순수함
≥99%
이름과 식별자
정식 스마일
C1C(C(CS1(=O)=O)S(=O)(=O)C2=CC(=C(C=C2)Cl)Cl)NCC(=O)O
IUPAC Name
2-[[(3S,4R)-4-(3,4-dichlorophenyl)sulfonyl-1,1-dioxothiolan-3-yl]amino]acetic acid
InChIKey
FNQDSYKGBCVHHI-QWRGUYRKSA-N
INCHI
1S/C12H13Cl2NO6S2/c13-8-2-1-7(3-9(8)14)23(20,21)11-6-22(18,19)5-10(11)15-4-12(16)17/h1-3,10-11,15H,4-6H2,(H,16,17)/t10-,11-/m0/s1
PubChem CID
155819525
분자량
402.27

고급 데이터

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
분류Carboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives
Direct ParentAlpha amino acids and derivatives
Alternative Parents Chlorobenzenes  Thiolanes  Sulfones  Amino acids  Monocarboxylic acids and derivatives  Dialkylamines  Carboxylic acids  Organopnictogen compounds  Organooxygen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Alpha-amino acid or derivatives - Halobenzene - Chlorobenzene - Benzenoid - Monocyclic benzene moiety - Thiolane - Sulfonyl - Sulfone - Amino acid - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Amine - Aromatic heteromonocyclic compound
설명This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors Not available
3D 구조
상호 작용 화학 구조 모델





인증서(CoA, COO, BSE/TSE 및 분석 차트)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
화학 및 물리적 특성
용해성DMSO : 200 mg/mL (497.18 mM; Need ultrasonic)
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