286583
5-Methoxytryptamine
97%
동의어(들):
2-(5-Methoxyindol-3-yl)ethylamine, 3-(2-Aminoethyl)-5-methoxyindole, 5-MOT, 5-Methoxyindole-3-ethanamine, Deacetylmelatonin, NSC 56422
로그인조직 및 계약 가격 보기
모든 사진(2)
About This Item
실험식(Hill 표기법):
C11H14N2O
CAS Number:
Molecular Weight:
190.24
Beilstein:
145587
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
형태
solid
mp
121-123 °C (lit.)
작용기
amine
SMILES string
COc1ccc2[nH]cc(CCN)c2c1
InChI
1S/C11H14N2O/c1-14-9-2-3-11-10(6-9)8(4-5-12)7-13-11/h2-3,6-7,13H,4-5,12H2,1H3
InChI key
JTEJPPKMYBDEMY-UHFFFAOYSA-N
유전자 정보
human ... HTR1A(3350) , HTR2A(3356) , HTR2C(3358)
rat ... Htr2a(29595) , Htr2c(25187) , Htr7(65032)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
관련 카테고리
일반 설명
The protective effect of 5-methoxytryptamine (a metabolite of melatonin) in human keratinocytes against ultraviolet B (UVB) radiation was studied.
애플리케이션
5-Methoxytryptamine was used as an agonist in the study of pharmacological profile of the 5-hydroxytryptamine 1 receptor.
Reactant for preparation of:
- Carboline disaccharide domain of shishijimicin A
- Melatonin analogs for the reduction of intraocular pressure
- 5-HT4 receptor ligands
- inhibitors of sortase A and isocitrate lyase
- Therapeutic agents for treatment of ischemia/reperfusion (I/R) injury
- Aurora and epidermal growth factor receptor kinase inhibitors
- Agents for the treatment of human papillomavirus infection
- Manzamine analogues for the control of neuroinflammation and cerebral infections
- Inhibitors of pro-inflammatory cytokines
- Tacrine-melatonin hybrids as multifunctional agents for alzheimer′s disease
포장
Bottomless glass bottle. Contents are inside inserted fused cone.
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
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Amir Hanna-Elias et al.
European journal of medicinal chemistry, 44(7), 2952-2959 (2009-02-19)
Twenty-three indole-3-methanamines were designed, synthesized and evaluated as ligands for the 5-HT(4) receptor. Compounds I-d, I-j, I-o, I-q and I-u showed good affinity at 100 microM and I-o was found to be only 5-fold less potent than the agonists serotonin
Melatonin and its metabolites ameliorate ultraviolet B-induced damage in human epidermal keratinocytes.
Janjetovic Z, Nahmias ZP, Hanna S, et al.
Journal of Pineal Research, 57(1), 90-102 (2014)
Hyun-Ji Kim et al.
Combinatorial chemistry & high throughput screening, 11(4), 316-324 (2008-05-14)
Continuous identification and validation of novel drug targets require the development of rapid, reliable, and sensitive cell-based high-throughput screening (HTS) methods for proposed targets. Recently, the 5-HT(6) receptor (5-HT(6)R), a member of the class of recently discovered 5-HT receptors, has
A Hanna-Elias et al.
Current medicinal chemistry, 17(25), 2775-2787 (2010-07-01)
For the development of novel 5-HT(4) receptor ligands we have designed and synthesized two series of 5-methoxytryptamine derivatives varying the substitution on the primary amine. Their biological activities were evaluated in a receptor binding assay where a subset of compounds
Anna Haduch et al.
Pharmacological research, 67(1), 53-59 (2012-10-27)
Brain serotonin has been implicated in the pathophysiology of a wide spectrum of psychiatric disorders, as well as in the mechanism of action of psychotropic drugs. The aim of present study was to identify rat cytochrome P450 (CYP) isoforms which
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.