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Target Snapshot

CHEMBL2007625 Target Snapshot

Isocitrate dehydrogenase [NADP] cytoplasmic · SINGLE PROTEIN · Homo sapiens

39,595Compounds
482Assays
8Approved Drugs
13,897.0Activities
Free Research Context

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Broader Open DB context

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Structured disease, protein, and project context should read before the lower-level identity rail.

As of 2026-09-13

Isocitrate dehydrogenase [NADP] cytoplasmic shows approved-linked disease relevance led by acute myeloid leukemia. 5 more disease programs remain visible in the same review block. 4 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt O75874. Start with acute myeloid leukemia, then reuse UniProt O75874 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with acute myeloid leukemia, then reuse UniProt O75874 as the stable protein anchor across project notes and exports.

ChEMBL component mapping + Open Targets-ready proxy + ChEMBL 36 via Core Engine 2026-09-13 4 linked drugs
Open source guide
Disease program
acute myeloid leukemia

Isocitrate dehydrogenase [NADP] cytoplasmic shows approved-linked disease relevance led by acute myeloid leukemia. 5 more disease programs remain visible in the same review block. 4 linked drugs remain visible in the same block.

Start review with acute myeloid leukemia because it currently carries approved-linked support. Linked drugs include BAY1436032, IDH305, IVOSIDENIB, OLUTASIDENIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Disease source · ChEMBL drug mechanism + indication proxy
Approved-linked Open Targets-ready proxy 4 linked drugs
Open disease block
Identity Layer

Cross-source identity

Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.

This review treats Isocitrate dehydrogenase [NADP] cytoplasmic as ChEMBL target CHEMBL2007625, mapped to UniProt O75874. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Isocitrate dehydrogenase [NADP] cytoplasmic
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL2007625
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
O75874
Isocitrate dehydrogenase [NADP] cytoplasmic
UniProt accession via ChEMBL component mapping As of 2026-09-13
www.uniprot.org
Disease evidence contract
Open Targets-ready proxy
ChEMBL drug mechanism + indication proxy
ChEMBL drug mechanism + indication proxy As of 2026-09-13
www.ebi.ac.uk

Reuse the same identifiers in notes, watch rules, exports, and review packs so provenance stays stable across surfaces.

Source Guidance

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Need stable target naming and protein identity?
UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether Isocitrate dehydrogenase [NADP] cytoplasmic is the right protein anchor across sources, using UniProt O75874 as the stable mapping.

Jump to Protein Context
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Disease Relevance & Evidence Level
ChEMBL drug mechanism + indication proxy

Use this block first when you need to confirm why acute myeloid leukemia is currently framed as approved-linked support. It currently carries 4 linked drugs in the same disease frame.

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Evidence Card
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Overview

Basic Information

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UniProt Context

UniProt Target Context

Reviewable protein naming and mapping context for this target snapshot.

Protein LabelIsocitrate dehydrogenase [NADP] cytoplasmic
UniProt AccessionO75874
Component TypeProtein
Sequence Length414 aa

Isocitrate dehydrogenase [NADP] cytoplasmic

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Isocitrate dehydrogenase [NADP] cytoplasmic, mapped to UniProt O75874. Sequence length is 414 aa.

Mapped IDO75874
Review nameIsocitrate dehydrogenase [NADP] cytoplasmic
OrganismHomo sapiens
Disease Relevance

Disease Relevance & Evidence Level

Open Targets-ready disease context using the current target-indication evidence contract.

Approved-linked Open Targets-ready proxy

Isocitrate dehydrogenase [NADP] cytoplasmic shows approved-linked disease relevance led by acute myeloid leukemia. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
acute myeloid leukemia
4 linked drugs · 4 direct · 4 efficacy
Linked drugBAY1436032
Linked drugIDH305
Linked drugIVOSIDENIB
Linked drugOLUTASIDENIB
Approved-linked Approved
cholangiocarcinoma
1 linked drug · 1 direct · 1 efficacy
Linked drugIVOSIDENIB
Late clinical Phase III
myelodysplastic syndrome
2 linked drugs · 2 direct · 2 efficacy
Linked drugIVOSIDENIB
Linked drugOLUTASIDENIB
Late clinical Phase III
biliary tract neoplasm
1 linked drug · 1 direct · 1 efficacy
Linked drugIVOSIDENIB
Clinical signal Phase II
cancer
2 linked drugs · 2 direct · 2 efficacy
Linked drugIDH305
Linked drugIVOSIDENIB
Clinical signal Phase II
Paraganglioma
2 linked drugs · 2 direct · 2 efficacy
Linked drugIDH305
Linked drugIVOSIDENIB
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with acute myeloid leukemia because it currently carries approved-linked support. Linked drugs include BAY1436032, IDH305, IVOSIDENIB, OLUTASIDENIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaseacute myeloid leukemia
Strongest levelApproved-linked
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

8
Approved
4
Phase II
2
Phase I
Assay Mix

Activity Type Distribution

IC5013,673.0
KI158.0
EC5014.0
KD52.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL4279047 10.4 IC50 0.04 Approved
CHEMBL4278845 9.6 IC50 0.25 Preclinical
CHEMBL4283785 9.52 IC50 0.3 Preclinical
CHEMBL5633097 9.46 IC50 0.349 Preclinical
CHEMBL4448475 9.37 EC50 0.43 Preclinical
CHEMBL4280132 9.15 IC50 0.7 Preclinical
CHEMBL4280772 9.0 IC50 1.0 Preclinical
CHEMBL4278793 9.0 IC50 1.0 Preclinical
CHEMBL4277352 9.0 IC50 1.0 Preclinical
CHEMBL3909586 9.0 IC50 1.0 Preclinical
Distribution

pChEMBL Value Distribution

1031
5.0
735
5.5
1920
6.0
1535
6.5
2206
7.0
992
7.5
331
8.0
48
8.5
14
9.0
2
9.5
pChEMBL
Approved Drugs

Approved Drugs

VORASIDENIB
CHEMBL4279047
Approved 2024
OLUTASIDENIB
CHEMBL4297610
Approved 2022
IVOSIDENIB
CHEMBL3989958
Approved 2018
ENASIDENIB
CHEMBL3989908
Approved 2017
Assay Landscape

Assay Landscape

482
Total Assays
4,668
Tested Compounds
3
Assay Types
Binding — 469 assays, 4,668 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 187 3,644 6.5
cell-based format 178 491 6.8
assay format 103 533 6.8
subcellular format 1 0
Functional — 12 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
organism-based format 7 0
assay format 4 0
cell-based format 1 0
ADME — 1 assays, 1 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 1 1 5.2

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine