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Merck
모든 사진(1)

주요 문서

SML3639

Sigma-Aldrich

CU-T12-9

≥98% (HPLC)

동의어(들):

CU-T 12-9, N-Methyl-4-nitro-2-(4-(4-(trifluoromethyl)phenyl)-1H-imidazol-1-yl)aniline

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About This Item

실험식(Hill 표기법):
C17H13F3N4O2
CAS Number:
Molecular Weight:
362.31
MDL number:
UNSPSC 코드:
12352200
NACRES:
NA.77

Quality Level

분석

≥98% (HPLC)

양식

powder

색상

white to beige

solubility

DMSO: 2 mg/mL, clear

저장 온도

-10 to -25°C

SMILES string

FC(F)(F)c1ccc(cc1)c2nc[n](c2)c3c(ccc(c3)[N+](=O)[O-])NC

InChI

1S/C17H13F3N4O2/c1-21-14-7-6-13(24(25)26)8-16(14)23-9-15(22-10-23)11-2-4-12(5-3-11)17(18,19)20/h2-10,21H,1H3

InChI key

LITXVDAFEYLWQE-UHFFFAOYSA-N

관련 카테고리

생화학적/생리학적 작용

Activator of toll-like receptor signaling, selective for TLR1 and TLR2
CU-T12-9 is a potent activator of toll-like receptor signaling, selective for TLR1 and TLR2. CU-T12-9 binds selectively to toll-like receptors TLR1 and TLR2, facilitating the TLR1/2 heterodimeric complex formation and activating downstream signaling of NF-κB.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Kui Cheng et al.
Science advances, 1(3) (2015-06-24)
Toll-like receptor (TLR) agonists activate both the innate and the adaptive immune systems. These TLR agonists have been exploited as potent vaccine adjuvants and antitumor agents. We describe the identification and characterization of a small molecule, N-methyl-4-nitro-2-(4-(4-(trifluoromethyl)phenyl)-1 H-imidazol-1-yl)aniline (CU-T12-9), that
Oxy210, a Semi-Synthetic Oxysterol, Exerts Anti-Inflammatory Effects in Macrophages via Inhibition of Toll-like Receptor (TLR) 4 and TLR2 Signaling and Modulation of Macrophage Polarization
International Journal of Molecular Sciences, 23(10), 5478-5478 (2022)
Tomoya Muto et al.
Cell stem cell, 29(2), 298-314 (2022-01-20)
Clonal hematopoiesis (CH) is an aging-associated condition characterized by the clonal outgrowth of pre-leukemic cells that acquire specific mutations. Although individuals with CH are healthy, they are at an increased risk of developing myeloid malignancies, suggesting that additional alterations are

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