Elvitegravir

Elvitegravir

SCHEMBL2280863

[2H]C([2H])([2H])Oc1cc2c(cc1Cc1cccc(Cl)c1F)c(=O)c(C(=O)O)cn2[C@H](CO)C(C)C

nearest known ligand 0.89

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 15)

geneUniProtsupporting neighboursconfidence
▸ METTL3 Q86U44 1/20 0.89
▸ PLA2G4A P47712 4/20 0.34
▸ MAPT P10636 2/20 0.33
▸ GAA P10253 2/20 0.33
▸ TP53 P04637 1/20 0.32
▸ CFD P00746 2/20 0.32
▸ EGFR P00533 2/20 0.32
▸ HTT P42858 1/20 0.32
▸ KDM4E B2RXH2 2/20 0.31
▸ POLB P06746 1/20 0.31
▸ ALDH1A1 P00352 1/20 0.31
▸ HPGD P15428 1/20 0.31
▸ TSHR P16473 1/20 0.31
▸ RAB9A P51151 1/20 0.31
▸ HSD17B10 Q99714 1/20 0.31

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 SCHEMBL13225651 0.94 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL726251 0.94 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL726252 0.94 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL29623981 0.94 METTL3 (1.00) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL1050769 0.94 METTL3 (0.98) METTL3PLA2G4AMAPTGAATP53
Elvitegravir SCHEMBL1050765 0.94 METTL3 (0.98) METTL3PLA2G4AMAPTGAATP53
SCHEMBL1045112 0.90 METTL3 (0.86) METTL3PLA2G4AMAPTGAATP53
SCHEMBL3245266 0.90 METTL3 (0.86) METTL3PLA2G4AMAPTGAATP53
SCHEMBL3118267 0.90 METTL3 (0.85) METTL3MAPTGAATP53CFD
Elvitegravir SCHEMBL31577400 0.90 METTL3 (0.88) METTL3PLA2G4AMAPTGAATP53

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2197847-B1 DEUTERATED 4 -OXOQUINOLINE DERIVATIVE FOR THE TREATMENT OF HIV INFECTION CONCERT PHARMACEUTICALS INC (US) 2012-11-07 — — EP disclosed
US-7994194-B2 4-oxoquinoline derivatives CONCERT PHARMACEUTICALS, INC. (US) 2011-08-09 — — US disclosed
US-7994194-B2 4-oxoquinoline derivatives CONCERT PHARMACEUTICALS, INC. (US) 2011-08-09 — — US disclosed
US-20090143427-A1 4-Oxoquinoline derivatives SUN PHARMACEUTICAL INDUSTRIES, INC. 2009-06-04 — — US disclosed
US-20090143427-A1 4-Oxoquinoline derivatives SUN PHARMACEUTICAL INDUSTRIES, INC. 2009-06-04 — — US disclosed

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

For each of this compound's patents that has machine-readable text (1 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-20090143427-A1 4-Oxoquinoline derivatives CYP3A4, PIK3CA, CYP3A5 METTL3 2275/4885PLA2G4A 2963/4885MAPT 2253/4885

“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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