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经验公式(希尔记法):
C34H38N4O4 · 2HCl
化学文摘社编号:
分子量:
639.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
273-141-0
MDL number:
InChI key
LLAQRSFKJHORNW-HXFTUNQESA-N
InChI
1S/C34H38N4O4.2ClH/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;;/h13-16,35,38H,7-12H2,1-6H3,(H,39,40)(H,41,42);2*1H/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;;
SMILES string
Cl.Cl.CCc1c(C)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(C)c5CCC(O)=O)c(CCC(O)=O)c4C)c(C)c3CC
assay
95%
reaction suitability
core: porphyrin, reagent type: catalyst
λmax
401 nm
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Shane C McAllister et al.
Pharmacogenomics, 6(3), 235-244 (2005-07-15)
Kaposi's sarcoma (KS) is a multifocal angioproliferative disorder affecting the skin, mucosa and viscera of individuals infected with human herpesvirus-8 (HHV-8; also Kaposi's sarcoma-associated herpesvirus [KSHV]). KS is the most common neoplasm in AIDS patients; the clinical outcome of AIDS-KS
Roxanne Kieltyka et al.
Methods in molecular biology (Clifton, N.J.), 608, 223-255 (2009-12-17)
Telomerase inhibition through guanine quadruplex sequestration by small-molecule drugs is of great current interest as an anticancer strategy. G-quadruplexes (GQs) can be formed at the guanine-rich sequences found at the end of the telomere. They possess a large electron-rich pi-surface
Naoki Hosomi et al.
Journal of bioscience and bioengineering, 99(3), 222-229 (2005-10-20)
Monoclonal antibody 2D7 generated against a transition-state analog N-methyl mesoporphyrin catalyzes a reaction for insertion of a cupric ion into mesoporphyrin. To investigate amino acid residues responsible for the catalytic activity, site-directed mutagenesis of the amino acid residues in the
J Koster et al.
The journal of physical chemistry. A, 110(39), 11252-11259 (2006-09-29)
The symmetry properties of selected vibrational modes of mesoporphyrin IX dimethyl ester (MP-IX-DME) in solution are investigated under different electronic resonance conditions. The Raman band parameters of the macrocycle modes nu(2), nu(10), nu(11), and nu(19) are determined from a quantitative
Monika S Walczak et al.
The journal of physical chemistry. B, 115(5), 1145-1150 (2010-12-31)
X-ray absorption spectroscopy is used to determine the local atomic structure around the iron atom from a soluble synthetic analogue of malaria pigment (hemozoin), cf. ferrimesoporphyrin IX of mesohematin anhydride, in the absence or presence of chloroquine (CQ) in dimethyl
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