Obicetrapib (DC10134) chemical structure
Chemical structureResearch use only
CAT. NO. DC10134Featured

Obicetrapib (AMG-899,TA-8995)

Pack size & price

USD
Total$750
We match the best price and quality on market.
Product overview

Description & Application

Obicetrapib, also known as TA-8995, is a CETP inhibitor for lipoprotein metabolism and cholesterol-efflux research.

ParameterValue
Chemical Name4-((2-((3,5-bis(trifluoromethyl)benzyl)((2R,4S)-1-(ethoxycarbonyl)-2-ethyl-6-
CAS No.866399-87-3
SynonymsAMG 899,TA 8995,AMG899,TA8995,
FormulaC32H31F9N4O5
M.Wt722.6
SMILESO=C(O)CCCOC1=CN=C(N(CC2=CC(C(F)(F)F)=CC(C(F)(F)F)=C2)[C@H]3C[C@@H](CC)N(C(OCC)=O)C4=C3C=C(C(F)(F)F)C=C4)N=C1
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
CETP · Literature evidence

Biological Activity

Obicetrapib, also known as TA-8995, is a CETP inhibitor for lipoprotein metabolism and cholesterol-efflux research. Published human study results are separated from preclinical assays below.

In Vitro

No separate compound-specific cell or biochemical result is available from the sources summarized here.

In Vivo

No compound-specific animal efficacy result is established by the sources summarized here.

Clinical / Human Evidence

EndpointModel / conditions / sourceReported result
Study design187 participants with mild dyslipidemia; randomized treatment for 12 weeks. [1]Compared placebo, TA-8995 1, 5 or 10 mg, and TA-8995 10 mg plus rosuvastatin 10 mg using serum lipoprotein and cholesterol-efflux endpoints.
Total cholesterol effluxParticipant serum tested in J774 macrophage-based assays; TA-8995 10 mg arm. [1]Total cholesterol-efflux capacity increased by 38% relative to placebo.
Efflux pathwaysSame 12-week study and dose arm. [1]Non-ABCA1 and ABCA1-specific efflux capacities increased by 72% and 28%, respectively.
HDL remodelingTA-8995 10 mg arm; serum HDL subclass analysis. [1]Preβ-1 HDL increased by 36%; changes correlated with ABCA1-mediated efflux. These are biomarker outcomes, not cardiovascular event outcomes.

Interpretation

These clinical biomarker results do not establish a cardiovascular-outcome benefit or describe the performance of a research reagent lot.

Original studies

References

  1. van Capelleveen JC, et al. Effects of the cholesteryl ester transfer protein inhibitor, TA-8995, on cholesterol efflux capacity and high-density lipoprotein particle subclasses. Journal of clinical lipidology (2016).

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

For additional quantities or product documentation, contact info@dcchemicals.com.

Related research products

Laropiprant chemical structureDC1009

Laropiprant

Laropiprant is a DP1 receptor antagonist for prostanoid signaling and platelet-function research. Its effects on platelet activation vary with agonist and concentration.

View activity & prices

Cart

Request quotation