Human immunodeficiency virus 2
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Human immunodeficiency virus 2 as ChEMBL target CHEMBL380. Disease framing currently uses the Open Targets-ready proxy contract.
Reuse the same identifiers in notes, watch rules, exports, and review packs so provenance stays stable across surfaces.
Why Human immunodeficiency virus 2 matters
Human immunodeficiency virus 2 is reviewed as Human immunodeficiency virus 2; the current evidence base includes 44 approved drugs, 4266 compounds, and 428 assays, with lead potency reaching pChEMBL 11.0.
Human immunodeficiency virus 2
Review this target as Human immunodeficiency virus 2.
Protein source · UniProt accession via ChEMBL component mappingDisease relevance is not yet populated for this evidence card.
This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
ChEMBL target recordChEMBL currently tracks 44 approved drugs, 4266 compounds, and 428 assays for this target. The dominant activity type is EC50. CHEMBL57548 is the current potency anchor at pChEMBL 11.0.
Use CHEMBL57548 as the tractability anchor when discussing potency (pChEMBL 11.0).
Activity source · ChEMBL 36 via Core EngineStart with the right source
Pick the first block or linked source that matches the review question in front of you.
Start with the review rationale when you need to explain why Human immunodeficiency virus 2 matters before drilling into raw source blocks.
Jump to Review RationaleGo back to the target snapshot when you need the naming and mapping contract, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need the disease program and supporting signals, not only the card summary.
Open Disease ContextSnapshot State
No project snapshot selected. Export uses the live evidence card state.
pChEMBL Activity Distribution
Top 5 Inhibitors (by pChEMBL)
| Structure | Compound | pChEMBL | Type | Phase |
|---|---|---|---|---|
|
|
No preferred name
CHEMBL57548
|
11.0 | IC50 | — |
|
|
No preferred name
CHEMBL513181
|
10.7 | EC50 | — |
|
|
No preferred name
CHEMBL5398494
|
10.7 | EC50 | — |
|
|
No preferred name
CHEMBL267571
|
10.6 | Ki | — |
|
|
No preferred name
CHEMBL104245
|
10.4 | EC50 | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
DOLUTEGRAVIR SODIUM
CHEMBL1213165
|
2013 |
|
|
TOFACITINIB
CHEMBL221959
|
2012 |
|
|
ELVITEGRAVIR
CHEMBL204656
|
2012 |
|
|
RUXOLITINIB
CHEMBL1789941
|
2011 |
|
|
INGENOL MEBUTATE
CHEMBL1863513
|
2010 |
|
|
PLERIXAFOR
CHEMBL18442
|
2008 |
|
|
ETRAVIRINE
CHEMBL308954
|
2008 |
|
|
RALTEGRAVIR
CHEMBL254316
|
2007 |
|
|
RALTEGRAVIR POTASSIUM
CHEMBL518520
|
2007 |
|
|
DARUNAVIR
CHEMBL1323
|
2006 |
|
|
TIPRANAVIR
CHEMBL222559
|
2005 |
|
|
EMTRICITABINE
CHEMBL885
|
2003 |
|
|
ENFUVIRTIDE
CHEMBL525076
|
2003 |
|
|
ATAZANAVIR
CHEMBL1163
|
2003 |
|
|
ADEFOVIR DIPIVOXIL
CHEMBL922
|
2002 |
|
|
TENOFOVIR DISOPROXIL
CHEMBL1538
|
2001 |
|
|
TENOFOVIR DISOPROXIL FUMARATE
CHEMBL1486
|
2001 |
|
|
LOPINAVIR
CHEMBL729
|
2000 |
|
|
AMPRENAVIR
CHEMBL116
|
1999 |
|
|
EFAVIRENZ
CHEMBL223228
|
1998 |
|
|
NELFINAVIR
CHEMBL584
|
1997 |
|
|
RITONAVIR
CHEMBL163
|
1996 |
|
|
LAMIVUDINE
CHEMBL141
|
1995 |
|
|
SAQUINAVIR
CHEMBL114
|
1995 |
|
|
STAVUDINE
CHEMBL991
|
1994 |
|
|
ZALCITABINE
CHEMBL853
|
1992 |
|
|
ZIDOVUDINE
CHEMBL129
|
1987 |