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Delavirdine

Cat. No. M28265
Delavirdine Structure
Synonym:

U 90152; BHAP-U 90152

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Biological Activity

Delavirdine (U 90152) is a potent, highly specific and orally active non-nucleoside reverse transcriptase inhibitor (NNRTI). Delavirdine selectively inhibits HIV-1 reverse transcriptase (RT) (IC50=0.26 μM) over DNA polymerase α (IC50=440 μM) and polymerase δ (IC50>550 μM). Delavirdine is an inhibitor of HIV-1 replication and can can be used for the study of AIDs.

Chemical Information
Molecular Weight 456.56
Formula C22H28N6O3S
CAS Number 136817-59-9
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] No authors listed. Delavirdine

[2] No authors listed. Delavirdine

[3] J Q Tran, et al. Clin Pharmacokinet. Delavirdine: clinical pharmacokinetics and drug interactions

[4] L J Scott, et al. Drugs. Delavirdine: a review of its use in HIV infection

[5] W W Freimuth. Adv Exp Med Biol. Delavirdine mesylate, a potent non-nucleoside HIV-1 reverse transcriptase inhibitor

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Keywords: Delavirdine, U 90152; BHAP-U 90152 supplier, HIV Protease, inhibitors, activators


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