Elvitegravir

Elvitegravir

SCHEMBL726251

COc1cc2c(cc1Cc1cccc(Cl)c1F)c(=O)c(C(=O)O)cn2C(CO)C(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

pol

The experimentally established mechanism targets of Elvitegravir. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ METTL3 Q86U44 1/20 1.00
▸ PLA2G4A P47712 5/20 0.39
▸ MAPT P10636 2/20 0.38
▸ GAA P10253 1/20 0.38
▸ TP53 P04637 1/20 0.37
▸ EGFR P00533 4/20 0.36
▸ LTB4R Q15722 1/20 0.35
▸ POLB P06746 1/20 0.35
▸ CMA1 P23946 1/20 0.34

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Elvitegravir SCHEMBL726252 1.00 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL29623981 1.00 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL13225651 1.00 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL1050769 0.99 METTL3 (0.98) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL1050765 0.99 METTL3 (0.98) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL2280863 0.94 METTL3 (0.89) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL31577400 0.94 METTL3 (0.88) METTL3PLA2G4AMAPTGAATP53
SCHEMBL4366707 0.94 METTL3 (0.88) METTL3PLA2G4AMAPTGAATP53
SCHEMBL1104875 0.93 METTL3 (0.88) METTL3PLA2G4AMAPTGAAEGFR
SCHEMBL19829420 0.93 METTL3 (0.88) METTL3PLA2G4AMAPTGAAEGFR

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 149 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3406596-A1 4-OXOQUINOLINE COMPOUND AND USE THEREOF AS HIV INTEGRASE INHIBITOR Japan Tobacco Inc. (JP) 2018-11-28 — — EP claimed
EP-3287130-A1 COMBINATIONS COMPRISING A 4-ISOQUINOLONE DERIVATIVE AND PROTEASE INHIBITORS Japan Tobacco Inc. (JP) 2018-02-28 — — EP claimed
US-20180029989-A1 STABLE CRYSTAL OF 4-OXOQUINOLINE COMPOUND JAPAN TOBACCO INC. (JP) 2018-02-01 — — US claimed
US-20140364389-A1 Combination Therapy JAPAN TOBACCO INC. (JP) 2014-12-11 — — US claimed
EP-2802315-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THEIR PREPARATION Gilead Sciences, Inc. (US) 2014-11-19 — — EP claimed
US-8633219-B2 Combination therapy JAPAN TOBACCO INC. (JP) 2014-01-21 — — US claimed
WO-2013106732-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THEIR PREPARATION GILEAD SCIENCES, INC. (US) 2013-07-18 — — WO claimed
EP-2452682-A1 Use of 6-(3-chloro-2-fluorobenzyl)-1-[(2s)-1-hydroxy-3-methylbutan-2-yl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or salt thereof for treating retrovirus infection Japan Tobacco, Inc. (JP) 2012-05-16 — — EP claimed
US-20120093917-A1 METNASE AND INTNASE INHIBITORS AND THEIR USE IN TREATING CANCER THE REGENTS OF THE UNIVERSITY OF NEW MEXICO 2012-04-19 — — US claimed
EP-2332538-A1 Combinations comprising a 4-isoquinolone derivative and anti-HIV agents Japan Tobacco, Inc. (JP) 2011-06-15 — — EP claimed
JP-2009525265-A — — 2009-07-09 — — JP claimed
WO-2009006199-A1 THERAPEUTIC COMPOSITIONS AND THE USE THEREOF GILEAD SCIENCES, INC. (US) 2009-01-08 — — WO claimed
WO-2009006203-A1 THERAPEUTIC COMPOSITIONS AND THE USE THEREOF GILEAD SCIENCES, INC. (US) 2009-01-08 — — WO claimed
EP-1976517-A1 METHODS FOR IMPROVING THE PHARMACOKINETICS OF HIV INTEGRASE INHIBITORS GILEAD SCIENCES, INC. (US) 2008-10-08 — — EP claimed
WO-2007079260-A9 METHODS FOR IMPROVING THE PHARMACOKINETICS OF HIV INTEGRASE INHIBITORS GILEAD SCIENCES INC (US) 2007-08-30 — — WO claimed
WO-2007079260-A1 METHODS FOR IMPROVING THE PHARMACOKINETICS OF HIV INTEGRASE INHIBITORS GILEAD SCIENCES, INC. (US) 2007-07-12 — — WO claimed
EP-1758581-A1 COMBINATIONS COMPRISING A 4-ISOQUINOLONE DERIVATIVE AND ANTI-HIV AGENTS Japan Tobacco, Inc. (JP) 2007-03-07 — — EP claimed
US-20050288326-A1 Combination therapy SHIONOGI & CO., LTD. (JP) 2005-12-29 — — US claimed
WO-2005112930-A1 COMBINATIONS COMPRISING A 4-ISOQUINOLONE DERIVATIVE AND ANTI-HIV AGENTS JAPAN TOBACCO INC. (JP) 2005-12-01 — — WO claimed
EP-1564210-A1 4-OXOQUINOLINE COMPOUNDS AND UTILIZATION THEREOF AS HIV INTEGRASE INHIBITORS JAPAN TOBACCO INC. (JP) 2005-08-17 — — EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050288326-A1 Combination therapy TYMP, TPMT, PNP METTL3 855/4885PLA2G4A 1042/4885MAPT 1794/4885
US-20120093917-A1 METNASE AND INTNASE INHIBITORS AND THEIR USE IN TREATING CANCER RNASE1, DCLRE1B, FEN1 METTL3 75/4885PLA2G4A 2658/4885MAPT 3716/4885
US-20140364389-A1 Combination Therapy TYMP, TPMT, PNP METTL3 855/4885PLA2G4A 1042/4885MAPT 1794/4885
US-20180029989-A1 STABLE CRYSTAL OF 4-OXOQUINOLINE COMPOUND KCNQ2, RCC1, SFPQ METTL3 133/4885PLA2G4A 4321/4885MAPT 626/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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