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At least 55 records · Page 3Linked to original sources
PubMed2003

Electronic structure of iron chlorins: characterization of bis(l-valine methyl ester)(meso-tetraphenylchlorin)iron(III)triflate and bis(l-valine methyl ester)(meso-tetraphenylchlorin)iron(II).

The synthesis and characterization of the two iron chlorin complexes [Fe(III)(TPC)(NH(2)CH(CO(2)CH(3))(CH(CH(3))(2)))(2)]CF(3)SO(3) (1) and Fe(II)(TPC)[(NH(2)CH(CO(2)CH(3))(CH(CH(3))(2))](2) (2) are reported. The crystal structure of complex 1 has been determined. The X-ray structure shows that the porphyrinate rings are weakly distorted. The metal-nitrogen distances to the reduced pyrrole N(4), 2.034(4) A, and to the pyrrole trans to it N(2), 2.012(4) A, are longer than the distances to the two remaining nitrogens [N(1), 1.996(4) A, and N(3), 1.984(4) A], leading to a core-hole expansion of the macrocycle due to the reduced pyrrole. The (1)H NMR isotropic shifts at 20 degrees C of the different pyrrole protons of 1 varied from -0.8 to -48.3 ppm according to bis-ligated complexes of low-spin ferric chlorins. The EPR spectrum of [Fe(TPC)(NH(2)CH(CO(2)CH(3))(CH(CH(3))(2)))(2)]CF(3)SO(3) (1) in solution is rhombic and gives the principal g values g(1) = 2.70, g(2) = 2.33, and g(3) = 1.61 (Sigmag(2) = 15.3). These spectroscopic observations are indicative of a metal-based electron in the d(pi) orbital for the [Fe(TPC)(NH(2)CH(CO(2)CH(3))(CH(CH(3))(2)))(2)]CF(3)SO(3) (1) complex with a (d(xy))(2)(d(xz)d(yz))(3) ground state at any temperature. The X-ray structure of the ferrous complex 2 also shows that the porphyrinate rings are weakly distorted. The metal-nitrogen distances to the reduced pyrrole N(4), 1.991(5) A, and to the pyrrole trans to it N(2), 2.005(6) A, are slightly different from the distances to the two remaining nitrogens [N(1), 1.988(5) A, and N(3), 2.015(5) A], leading to a core-hole expansion of the macrocycle due to the reduced pyrrole.

Crystallography, X-Ray↗
PubMed1977

Hemoglobin S Travis: a sickling hemoglobin with two amino acid substitutions [beta6(A3)glutamic acid leads to valine and beta142 (h20) alanine leads to valine).

Hb S Travis is a previously undescribed sickling hemoglobin with two amino acid substitutions in the beta chain: beta6 Glu leads to Val and beta142 Ala leads to Val. The beta6 Glu leads to Val mutation imparts to Hb S Travis the characteristic properties of sickling hemoglobin, namely its association with erythrocyte sickling, the insolubility of the hemoglobin in the reduced form, and a minimum gelling concentration value identical to Hb S. Unlike Hb S, Hb S Travis exhibits an increased oxygen affinity and a decreased affinity for 2,3-bisphosphoglycerate and inositol hexakisphosphate. In addition, the variant hemoglobin's tendency to autoxidize and its mechanical precipitability suggest that there are conformational differences between Hb S and Hb S Travis.

Alanine↗
PubMed2005

Ratios of N-(2,3,4-trihydroxybutyl) valine and N-(2-hydroxy-3-butenyl) valine formed hemoglobin adducts in female mice inhalation exposure with 1,3-butadiene.

1,3-Butadiene (BD) is a known rodent and probable human carcinogen (IARC, group 2A) or 'known to be a human carcinogen' (Department of Health and Human Services, 2000). Exposure to BD can occur either via petrochemical products or through the general environment. Adducts can be used as biomarkers for biological monitoring of carcinogen exposure. This study investigated the hemoglobin adducts in blood after inhalation exposure to BD in ICR female mice for three weeks (5 h/day x 5 days/week). During the inhalation exposure, the body weights of mice were significantly lower from day 9 onward for the 500 ppm BD group and from day 4 onward for the 1000 ppm BD group. On the 1st, 2nd and 3rd weeks after inhalation exposure, the concentrations of HB Val adducts were 1.8, 3.7 and 6.2 pmol/mg globin for the 500 ppm BD group, and 5.7, 7.4 and 16.0 pmol/mg globin for the 1000 ppm BD group. The concentrations of THB Val adducts were 32.0, 42.0 and 55.0 pmol/mg globin for the 500 ppm BD group, and 67.8, 72.7 and 83.5 pmol/mg globin for the 1000 ppm BD group. Their defined ratios were higher at the earlier exposure period and at the lower concentration. They were 17.8, 11.4 and 8.87 for the 500 ppm BD group, and 11.9, 9.8 and 5.2 for the 1000 ppm BD group, on the 1st, 2nd and 3rd weeks after inhalation exposure. THB Val and HB Val adducts appear to be the important hemoglobin adducts for monitoring BD exposure, with the latter being a more predictable biomarker than the former.

Administration, Inhalation↗
PubMed1992

Valine deficiency. 2. The effect of feeding a valine-deficient diet during the starter period on performance and leg abnormality of male broiler chicks.

Using force-feeding and pair-feeding techniques, two experiments were conducted to investigate the problem of leg abnormality associated with feeding a Val-deficient diet as compared with a diet deficient in all the branched chain amino acids (BCAA) or a Val-supplemented diet. The BCAA-deficient diet contained .96, .52, and .63% of Leu, Ile, and Val, respectively. The Val-deficient diet contained 1.37 Leu, .82 Ile, and .63% Val. The Val-supplemented diet contained 1.37 Leu, .82 Ile, and .83% Val. In both studies birds fed the Val-supplemented gained more weight than birds in the other two groups. Although birds on Val-deficient and BCAA-deficient diets had similar weight gain, the former were lethargic and showed feather and leg abnormalities. Bone ash and bone calcium for Val-deficient birds were the lowest among the three groups studied (P < .05). The levels of the BCAA in plasma reflected those of the treatment diets. Plasma hydroxyproline was lowest in birds fed the Val-deficient diet (P < .05), indicating a reduction in bone collagen breakdown. Kidney function measurements were the same for birds on the Val-supplemented and Val-deficient diets. Fractional excretion of calcium in Val-deficient birds (.13%), however, was three times higher than that of Val-supplemented birds (P < .05). The results indicated that Val deficiency per se increased calcium excretion in urine and induced leg abnormality in young chickens.

Amino Acids↗