| Weight | 164.116 g/mol |
|---|---|
| Formula | C8H4O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-Hydroxyphthalic anhydride (37418-88-5)
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- Bovine beta-lactoglobulin modified by 3-hydroxyphthalic anhydride blocks the CD4 cell receptor for HIV. (Nature Medicine, 1996)
- 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin Exhibits Potent and Broad Anti-HIV-1 Activity: a Potential Microbicide for Preventing Sexual Transmission of HIV-1 (Antimicrobial Agents and Chemotherapy, 2010)
- Glycodelins GdA and GdS modified by 3-hydroxyphthalic anhydride inhibit gp120-CD4 binding and HIV-1 infection in vitro. (Laboratory Investigation, 1997)
- 3-Hydroxyphthalic anhydride-modified human serum albumin as a microbicide candidate inhibits HIV infection by blocking viral entry (Journal of Antimicrobial Chemotherapy, 2013)
- Combinations of 3-Hydroxyphthalic Anhydride-Modified Ovalbumin With Antiretroviral Drug-Based Microbicide Candidates Display Synergistic and Complementary Effects Against HIV-1 Infection (Journal of Acquired Immune Deficiency Syndromes, 2011)
- A Versatile Synthetic Route to 3-Hydroxyphthalic Anhydride (Synthesis, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C(=C1)O)C(=O)OC2=O
-
InChIKeyCCTOEAMRIIXGDJ-UHFFFAOYSA-N
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