- 1. 1,2,3,4,4a,4b,7,9,10,10a-Decahydro-2-hydroxy-2,4b-dimethyl-7-oxo-1-phenanthrenepropionic Acid Delta-Lactone
- [A progesterone derivative with antineoplastic activity. Testolactone inhibits steroid aromatase, thereby preventing the formation of estrogen from adrenal androstenedione and reducing endogenous estrogen levels. (NCI04) ( NCI )] (UMLS (NCI) C0039600) =Steroid; Pharmacologic Substance; Hormone =Androstadienes;
Homosteroids;
[AN500] ANTINEOPLASTIC HORMONES;
=TESTOLACTONE 50 MG | - 6. Abagovomab
- [A murine immunoglobulin G1 (IgG1) monoclonal anti-idiotype antibody (ACA125). Vaccination with abagovomab may stimulate the host immune system to mount an antibody response and subsequent antibody-dependent cell-mediated cytotoxicity response against CA125 positive tumor cells, thereby decreasing tumor growth. (NCI04) ( NCI )] (UMLS (NCI) C1327946) Monoclonal Antibody ACA125 Anti-Idiotype Vaccine =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Immunologic Factor
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- 2. 1-ABaP
- [A polycyclic aromatic hydrocarbon belongs to the family of mutagen benzo(a)pyrene. 1-aminobenzo(a)pyrene consists of five fused rings with an amino-group attached to the first carbon atom of the aromatic hydrocarbon ring with potential carcinogenicity. ( NCI )] (UMLS (NCI) C0768966) 1-Aminobenzo[a]pyrene;
=Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance | - 7. abalone
- [ ] (UMLS (CSP) C0598488) =Invertebrate ;
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- 3. 3-ABaP
- [A polycyclic aromatic hydrocarbon belongs to the family of mutagen benzo(a)pyrene. 3-aminobenzo(a)pyrene consists of five fused rings with an amino-group attached to the third carbon atom of the aromatic hydrocarbon ring with potential carcinogenicity. ( NCI )] (UMLS (NCI) C0768968) 3-Aminobenzo[a]pyrene;
=Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance | - 8. Abandonment or neglect of infants and helpless persons
- [ ] (UMLS (ICD9CM) C0261659) =Human-caused Phenomenon or Process
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- 4. Abacavir
- [A synthetic carbocyclic nucleoside analog. In vivo, the activated triphosphate metabolite of abacavir is incorporated into the viral DNA instead of the natural substrate deoxyguanosine, thereby inhibiting human immunodeficiency virus (HIV) reverse transcriptase (RT) and, so, the replication of the viral DNA and infectious viral particles. This agent decreases HIV viral loads, retards or prevents the damage to the immune system, and reduces the risk of developing AIDS. ( NCI )] (UMLS (NCI) C0663655) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
=[AM800] ANTIVIRALS;
deoxyribonucleoside;
Reverse Transcriptase Inhibitor;
1592U89 =Abacavir Sulfate;
| - 9. Abasic Site Formation
- [Abasic Site Formation involves the creation of an apurinic or apyrimidinic site resulting from the loss of a purine or pyrimidine residue from DNA. ( NCI )] (UMLS (NCI) C1510710) Formation of Abasic Site;
=Cell or Molecular Dysfunction |
- 5. Abacavir Sulfate
- [The sulfate salt form of abacavir, a synthetic carbocyclic nucleoside analog. In vivo, the activated triphosphate metabolite of abacavir is incorporated into the viral DNA instead of the natural substrate deoxyguanosine, thereby inhibiting human immunodeficiency virus (HIV) reverse transcriptase (RT) and, so, the replication of the viral DNA and infectious viral particles. This agent decreases HIV viral loads, retards or prevents the damage to the immune system, and reduces the risk of developing AIDS. ( NCI )] (UMLS (NCI) C0724515) ABACAVIR SULFATE PREPARATION;
=Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
=Abacavir;
=ABACAVIR SULFATE 100 MG/5ML;
ABACAVIR SULFATE 300 MG;
| - 10. Abatement of event after product withdrawn
- (UMLS (HL7) C1546994) =Idea or Concept =Causality Observations;
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