MedKoo Cat#: 462843 | Name: U 88204

Description:

WARNING: This product is for research use only, not for human or veterinary use.

U 88204 is a non-nucleoside HIV-1 reverse transcriptase inhibitor.

Chemical Structure

U 88204
U 88204
CAS#136816-76-7

Theoretical Analysis

MedKoo Cat#: 462843

Name: U 88204

CAS#: 136816-76-7

Chemical Formula: C21H25N5O

Exact Mass: 363.2059

Molecular Weight: 363.47

Elemental Analysis: C, 69.40; H, 6.93; N, 19.27; O, 4.40

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
U-88204; U-88204E;
IUPAC/Chemical Name
(1H-indol-2-yl)(4-(3-(isopropylamino)pyridin-2-yl)piperazin-1-yl)methanone
InChi Key
ASOMNDIOOKDVDC-UHFFFAOYSA-N
InChi Code
InChI=1S/C21H25N5O/c1-15(2)23-18-8-5-9-22-20(18)25-10-12-26(13-11-25)21(27)19-14-16-6-3-4-7-17(16)24-19/h3-9,14-15,23-24H,10-13H2,1-2H3
SMILES Code
CC(C)NC1=CC=CN=C1N(CC2)CCN2C(C3=CC4=CC=CC=C4N3)=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 363.47 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Dueweke TJ, Kézdy FJ, Waszak GA, Deibel MR Jr, Tarpley WG. The binding of a novel bisheteroarylpiperazine mediates inhibition of human immunodeficiency virus type 1 reverse transcriptase. J Biol Chem. 1992 Jan 5;267(1):27-30. PMID: 1370445. 2: Vasudevachari MB, Battista C, Lane HC, Psallidopoulos MC, Zhao B, Cook J, Palmer JR, Romero DL, Tarpley WG, Salzman NP. Prevention of the spread of HIV-1 infection with nonnucleoside reverse transcriptase inhibitors. Virology. 1992 Sep;190(1):269-77. doi: 10.1016/0042-6822(92)91213-e. PMID: 1382341. 3: Balzarini J, Karlsson A, Meichsner C, Paessens A, Riess G, De Clercq E, Kleim JP. Resistance pattern of human immunodeficiency virus type 1 reverse transcriptase to quinoxaline S-2720. J Virol. 1994 Dec;68(12):7986-92. doi: 10.1128/JVI.68.12.7986-7992.1994. PMID: 7525984; PMCID: PMC237261. 4: Althaus IW, Chou JJ, Gonzales AJ, Deibel MR, Chou KC, Kezdy FJ, Romero DL, Palmer JR, Thomas RC, Aristoff PA, et al. Kinetic studies with the non- nucleoside HIV-1 reverse transcriptase inhibitor U-88204E. Biochemistry. 1993 Jul 6;32(26):6548-54. doi: 10.1021/bi00077a008. PMID: 7687145.