Pages that link to "Q44104976"
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The following pages link to A QSAR investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 1. Mutagenicity of aromatic and heteroaromatic amines in Salmonella typhimurium TA98 and TA100. (Q44104976):
Displaying 44 items.
- Current status of methods for defining the applicability domain of (quantitative) structure-activity relationships. The report and recommendations of ECVAM Workshop 52 (Q30066516) (← links)
- QSAR applicabilty domain estimation by projection of the training set descriptor space: a review (Q30066530) (← links)
- Frontier orbital energies, hydrophobicity and steric factors as physical QSAR descriptors of molecular mutagenicity. A review with a case study: MX compounds (Q33608909) (← links)
- Domain of EPI suite biotransformation models (Q33684808) (← links)
- An investigation into pharmaceutically relevant mutagenicity data and the influence on Ames predictive potential (Q34080242) (← links)
- Carcinogenicity of the aromatic amines: from structure-activity relationships to mechanisms of action and risk assessment (Q34712742) (← links)
- Approaches to developing alternative and predictive toxicology based on PBPK/PD and QSAR modeling (Q34942082) (← links)
- Biomonitoring of arylamines and nitroarenes (Q35001236) (← links)
- Hemoglobin binding of arylamines and nitroarenes: molecular dosimetry and quantitative structure-activity relationships (Q35031071) (← links)
- The expanding role of predictive toxicology: an update on the (Q)SAR models for mutagens and carcinogens (Q36761869) (← links)
- Alternatives to the carcinogenicity bioassay: in silico methods, and the in vitro and in vivo mutagenicity assays (Q37741223) (← links)
- Extended quantitative structure-activity relationships for 80 aromatic and heterocyclic amines: structural, electronic, and hydropathic factors affecting mutagenic potency (Q38455359) (← links)
- Structural and quantum chemical factors affecting mutagenic potency of aminoimidazo-azaarenes (Q38466140) (← links)
- Extending (Q)SARs to incorporate proprietary knowledge for regulatory purposes: A case study using aromatic amine mutagenicity (Q39995307) (← links)
- Prediction of mutagenicity utilizing a hierarchical QSAR approach (Q40663853) (← links)
- Review of mutagenicity of monocyclic aromatic amines: quantitative structure–activity relationships (Q41560466) (← links)
- Enhancing the flexibility and adaptability of the DARC structural representation for computer-aided drug design (Q41727783) (← links)
- Evaluation of 5-aminoisoquinoline (5-AIQ), a novel PARP-1 inhibitor for genotoxicity potential in vitro and in vivo (Q43183965) (← links)
- The effects of 4'-alkyl substituents on the mutagenic activity of 4-amino- and 4-nitrostilbenes in Salmonella typhimurium (Q43565145) (← links)
- Transformation of mutagenic aromatic amines into non-mutagenic species by alkyl substituents. Part I. Alkylation ortho to the amino function (Q43774702) (← links)
- Transformation of mutagenic aromatic amines into non-mutagenic species by alkyl substituents. Part II: alkylation far away from the amino function (Q43928280) (← links)
- The potential applications of SOS-lux biosensors for rapid screening of mutagenic chemicals (Q44341725) (← links)
- ANVAS: artificial neural variables adaptation system for descriptor selection (Q46704259) (← links)
- Quantitative Structure-Activity Relationship Model for HCVNS5B inhibitors based on an Antlion Optimizer-Adaptive Neuro-Fuzzy Inference System (Q47549119) (← links)
- In-Silico Screening of High Production Volume Chemicals for Mutagenicity using the mcase QSAR Expert System (Q47563561) (← links)
- Resolution of contradiction between in silico predictions and Ames test results for four pharmaceutically relevant impurities (Q47736441) (← links)
- Predictivity and reliability of QSAR models: the case of mutagens and carcinogens (Q50065385) (← links)
- Mechanistic QSAR of aromatic amines: new models for discriminating between homocyclic mutagens and nonmutagens, and validation of models for carcinogens (Q50066705) (← links)
- Mutagenic activities and physicochemical properties of selected nitrobenzanthrones (Q50076379) (← links)
- From mutagenic to non-mutagenic nitroarenes: effect of bulky alkyl substituents on the mutagenic activity of nitroaromatics in Salmonella typhimurium. Part II. Substituents far away from the nitro group (Q50121453) (← links)
- SOS chromotest results in a broader context: empirical relationships between genotoxic potency, mutagenic potency, and carcinogenic potency (Q50141055) (← links)
- Tolerance space and molecular similarity (Q50145367) (← links)
- Substituent effects on the genotoxicity of 4-nitrostilbene derivatives (Q50146876) (← links)
- QSAR models for both mutagenic potency and activity: application to nitroarenes and aromatic amines (Q50154407) (← links)
- On the mutagenicity of MX compounds (Q50162786) (← links)
- Quantitative structure-activity relationship investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 2. Mutagenicity of aromatic and heteroaromatic nitro compounds inSalmonella typhimurium TA100 (Q50181252) (← links)
- Structure-activity relationship of genotoxic polycyclic aromatic nitro compounds: further evidence for the importance of hydrophobicity and molecular orbital energies in genetic toxicity (Q50181937) (← links)
- Evaluation of QSAR models for the prediction of ames genotoxicity: a retrospective exercise on the chemical substances registered under the EU REACH regulation (Q50425075) (← links)
- (Q63611095) (← links)
- Predicting mutagenicity of chemicals using topological and quantum chemical parameters: A similarity based study (Q72049100) (← links)
- Rodent carcinogenicity and toxicity, in vitro mutagenicity, and their physical chemical determinants (Q72098999) (← links)
- Prediction of the genotoxicity of aromatic and heteroaromatic amines using electrotopological state indices (Q73711688) (← links)
- Mechanistic Category Formation for the Prediction of Respiratory Sensitization (Q84632547) (← links)
- Semi-correlations combined with the index of ideality of correlation: a tool to build up model of mutagenic potential (Q90733897) (← links)