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安全信息

54238

Supelco

地蒽酚

puriss. p.a., matrix substance for MALDI-MS, ≥98.5% (HPLC)

别名:

1,8,9-蒽三酚, 1,8-二羟基蒽-9(10H)-酮, 二羟蒽酚, 蒽林

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About This Item

经验公式（希尔记法）:
C14H10O3
CAS号:
1143-38-0
分子量:
226.23
Beilstein:
2054360
EC 号:
214-538-0
MDL编号:
MFCD00053409
UNSPSC代码:
12000000

等级

matrix substance for MALDI-MS
puriss. p.a.

方案

≥98.5% (HPLC)

mp

178-181 °C (lit.)

痕量阳离子

Ba: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤20 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤10 mg/kg

λmax

337 nm at >2000

储存温度

2-8°C

SMILES字符串

Oc1cccc2Cc3cccc(O)c3C(=O)c12

InChI

1S/C14H10O3/c15-10-5-1-3-8-7-9-4-2-6-11(16)13(9)14(17)12(8)10/h1-6,15-16H,7H2

InChI key

NUZWLKWWNNJHPT-UHFFFAOYSA-N

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Ulrich Kratz et al.
European journal of medicinal chemistry, 45(11), 5278-5285 (2010-09-11)
A series of 10-substituted 4,5-dichloro-10H-anthracen-9-ones were synthesized in the search for novel agents against keratinocyte hyperproliferation. The antiproliferative activity of these novel anthrones was evaluated using the human keratinocyte line HaCaT as the primary test system. Structure-activity relationships with respect
Aleksandar Putic et al.
European journal of medicinal chemistry, 45(11), 5345-5352 (2010-09-21)
A series of 10-substituted hydroxy-10H-acridin-9-ones were synthesized and studied as potential antipsoriatic agents. The antiproliferative activity of the novel derivatives, which can be considered as aza-analogues of the antipsoriatic drug anthralin, was determined using the human keratinocyte cell line HaCaT.
Aleksandar Putic et al.
European journal of medicinal chemistry, 45(8), 3299-3310 (2010-05-11)
A series of N-unsubstituted hydroxy-10H-acridin-9-ones were synthesized and evaluated for inhibitory action against HaCaT keratinocyte growth, in order to explore their potential as antipsoriatic agents. For structure-activity relationship studies, the number and position of the hydroxyl groups were modified, the
Denis Fourches et al.
Chemical research in toxicology, 23(1), 171-183 (2009-12-18)
Drug-induced liver injury is one of the main causes of drug attrition. The ability to predict the liver effects of drug candidates from their chemical structures is critical to help guide experimental drug discovery projects toward safer medicines. In this

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