IDH1 Drug Discovery Landscape & Assay Solutions

Market Intelligence, Clinical Progress, and High-Purity Reagents for Oncology Development.

TarMart Solution Ecosystem & Related Targets

Comprehensive reagent toolkit for IDH1 drug discovery. Select your modality below:

Component / Network Product Description Product Link
Antigen IDH1 WT & Mutant (R132H/R132C/R132S/R132G) Proteins
High purity (>95%), Endotoxin <1EU/ug. Sequence Verified. Theoretical MW confirmed.
View IDH1 Products
Gene Delivery IDH1 Promise-ORF / Lentivirus
Full-length ORF for stable mutant cell lines.
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Benchmark Ab Anti-IDH1 (R132H Specific)
Sequence Verified recombinant positive control for IHC/WB.
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Validator IDH1 siRNA Set
For specific knockdown verification in cell lines.
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Related Target A IDH2
Isoform counter-screening and dual-inhibition targeting.
View IDH2 Products
Related Target B TET2
Downstream epigenetic target affected by 2-HG accumulation.
View TET2 Products
Critical Assay Challenge The TarMart Advantage (Technical Spec)
Mutant vs. Wild-Type Selectivity Comprehensive panel of IDH1 mutants (R132H, R132C, R132S, R132G) and WT proteins available with >95% purity for precision enzymatic assays. Matched pair of WT and R132H proteins (SEC verified) for orthogonal selectivity screening.
Isoform Cross-Reactivity (IDH1 vs IDH2) High-purity IDH2 WT and mutant homolog proteins (including R140Q, R172K) strictly verified by mass spectrometry for reliable counter-screening.
Acquired Resistance Profiling Expanded IDH1 mutant panel (R132C, R132G, R132S, R132L) covering clinical resistance spectra for next-generation inhibitor screening.
Species Translation (Cyno/Mouse) Human/Mouse/Cyno ortholog proteins available with identical purity standards (>95%) for preclinical PK/PD evaluation.
Detection & Cellular Controls Sequence-verified mutant-specific recombinant antibodies for assay benchmarking. High-efficiency siRNA and IDH1 ORF Lentivirus (R132H) for generating stable isogenic lines and target-specificity validation.

Live IDH1 R&D Tracker

Market data changes daily. Access the latest global pipeline status directly:

Global Clinical Landscape & Future Outlook

The race for IDH1 therapeutics is intensifying. First-generation inhibitors (ivosidenib, olutasidenib) have established standard of care in AML and cholangiocarcinoma. Servier's vorasidenib (Voranigo), a brain-penetrant dual IDH1/2 inhibitor, recently expanded the landscape into low-grade glioma, answering a critical need for CNS-active therapies. As acquired resistance mutations (R132C, R132G, R132S, R132L) emerge in relapsed patients, the next wave of R&D focuses on next-generation allosteric inhibitors with broader mutant coverage, rational combination regimens with hypomethylating agents (azacitidine) or BCL-2 inhibitors (venetoclax), and novel modalities such as PROTACs and mutant neoantigen vaccines. TarMart supports this evolution with precision mutant proteins that enable differentiation between wild-type inhibition liabilities and mutant-specific potency, as well as species orthologs for translational studies.

Competitive Modality & Indication Snapshot

Modality Representative Players Key Indications Critical Assay Need (Why TarMart?)
Small Molecule (Allosteric) Servier (Ivosidenib), Rigel/Forma (Olutasidenib) AML, Cholangiocarcinoma Mutant vs WT Selectivity Assay (Need high-purity R132H and WT proteins)
Brain-Penetrant Inhibitor Servier (Vorasidenib) Low-Grade Glioma, Astrocytoma Dual IDH1/2 Specificity Profiling (Need IDH1 & IDH2 recombinant proteins)
Combination Regimen BMS, AbbVie, Agios/Servier AML, MDS Synergy & 2-HG Inhibition Assay (Need stable mutant cell lines via lentivirus)
PROTAC / Degrader Preclinical Biotech Refractory AML / Solid Tumors Ternary Complex & Target Engagement (Need full-length ORF and mutant proteins)
Vaccine / TCR-T Bayer, Transgene, Nouscom Glioma (Mutant Neoantigen) Peptide Presentation (Need sequence-verified antigen control)