SML2392
DREADD Agonist 21 dihydrochloride
≥98% (HPLC), powder, DREADD agonist
동의어(들):
11-(1-piperazinyl)-5H-Dibenzo[b,e][1,4]diazepine dihydrochloride, 11-(Piperazin-1-yl)-5H-dibenzo[b,e][1,4]diazepine; 11-Piperazinyldibenzo[b,e][1,4]diazepine dihydrochloride, Compound 21 dihydrochloride
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C17H18N4 · 2HCl
CAS Number:
Molecular Weight:
351.27
MDL number:
UNSPSC 코드:
12352200
NACRES:
NA.77
추천 제품
제품명
DREADD Agonist 21 dihydrochloride, ≥98% (HPLC)
분석
≥98% (HPLC)
양식
powder
저장 조건
desiccated
색상
yellow to brown
solubility
H2O: 2 mg/mL, clear
저장 온도
−20°C
SMILES string
C1(C=CC=C2)=C2C(N3CCNCC3)=NC(C=CC=C4)=C4N1
InChI
1S/C17H18N4/c1-2-6-14-13(5-1)17(21-11-9-18-10-12-21)20-16-8-4-3-7-15(16)19-14/h1-8,18-19H,9-12H2
InChI key
JCBYXNSOLUVGTF-UHFFFAOYSA-N
생화학적/생리학적 작용
Compound 21 is a potent designer drug with full agonist activity toward human hM3Dq (EC50 = 1.7 nM by cell-based Ca2+ mobilization assay), a human M3 muscarinic receptor (M3R)-based Gq (M3Dq) DREADD (Designer Receptors Exclusively Activated by Designer Drugs), displaying little activity toward muscarinic acetylcholine receptor M3 (30% M3 activation at 10 μM) and reduced affinity toward H1, 5HT2A, 5HT2C, α1A receptor (fold selectivity = 3.5, 40, 100, 165, respectively). Note: the DREADD hM3Dq exhibits M3 biological activity, but is insensitive to the endogenous ligand acetylcholine (ACh).
Potent designer drug with selective agonist activity for human M3Dq (hM3Dq) DREADD (Designer Receptors Exclusively Activated by Designer Drugs).
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Xin Chen et al.
ACS chemical neuroscience, 6(3), 476-484 (2015-01-15)
Over the past decade, two independent technologies have emerged and been widely adopted by the neuroscience community for remotely controlling neuronal activity: optogenetics which utilize engineered channelrhodopsin and other opsins, and chemogenetics which utilize engineered G protein-coupled receptors (Designer Receptors
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