Atazanavir

Atazanavir

SCHEMBL825777

COC(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C(C)(C)C.COC(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C(C)(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ UGT1A1 P22309 3/20 1.00
▸ MLNR O43193 1/20 1.00
▸ NR1I2 O75469 1/20 1.00
▸ SLCO2B1 O94956 1/20 1.00
▸ ABCB11 O95342 1/20 1.00
▸ ABCB1 P08183 1/20 1.00
▸ CCKAR P32238 1/20 1.00
▸ OPRK1 P41145 1/20 1.00
▸ GHSR Q92847 1/20 1.00
▸ SLCO1B3 Q9NPD5 1/20 1.00
▸ ABCG2 Q9UNQ0 1/20 1.00
▸ SLCO1B1 Q9Y6L6 1/20 1.00
▸ KCNH2 Q12809 1/20 0.72
▸ CTSD P07339 4/20 0.57
▸ CYP3A4 P08684 3/20 0.57
▸ CTSE P14091 1/20 0.41
▸ PGC P20142 1/20 0.41
▸ PSEN1 P49768 8/20 0.40
▸ PSEN2 P49810 8/20 0.40
▸ APH1B Q8WW43 8/20 0.40

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
Atazanavir SCHEMBL7993264 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL41697 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL41696 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL9975220 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL1559640 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL20629941 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL21565117 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL20629937 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL22847477 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11
Atazanavir SCHEMBL1396072 1.00 UGT1A1 (1.00) UGT1A1MLNRNR1I2SLCO2B1ABCB11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10869921-B2 Compositions and methods to treat AIDS UNIVERSITY OF MASSACHUSETTS (US) 2020-12-22 — — US disclosed
US-20190160165-A1 COMPOSITIONS AND METHODS TO TREAT AIDS UNIVERSITY OF MASSACHUSETTS 2019-05-30 — — US disclosed
EP-3452483-A1 ENHANCER OF ZESTE HOMOLOG 2 INHIBITORS GlaxoSmithKline Intellectual Property (No. 2) Limited (GB) 2019-03-13 — — EP disclosed
EP-3384040-A1 COMPOSITIONS FOR CYP450 PHENOTYPING USING SALIVA SAMPLES Concordia University, Inc. (US) 2018-10-10 — — EP disclosed
WO-2017191545-A1 ENHANCER OF ZESTE HOMOLOG 2 INHIBITORS GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2017-11-09 — — WO disclosed
WO-2017095921-A1 COMPOSITIONS FOR CYP450 PHENOTYPING USING SALIVA SAMPLES CONCORDIA UNIVERSITY INC. (US) 2017-06-08 — — WO disclosed
US-20160038502-A1 HIV TREATMENT FORMULATION OF ATAZANAVIR AND COBICISTAT BRISTOL-MYERS SQUIBB COMPANY 2016-02-11 — — US disclosed
WO-2012006353-A1 DRUG-ELUTING CERVICAL CAP CERMED CORPORATION (US) 2012-01-12 — — WO disclosed
EP-2190461-A2 USE OF PARATHYROID HORMONE (1-34) AS ANTI-HIV AGENT Mondobiotech Laboratories AG (LI) 2010-06-02 — — EP disclosed
EP-2187934-A1 USE OF FERTIRELIN AND DELTA-ENDORPHIN AS THERAPEUTIC AGENTS Mondobiotech Laboratories AG (LI) 2010-05-26 — — EP disclosed
WO-2009033663-A1 USE OF FERTIRELIN AND DELTA-ENDORPHIN AS THERAPEUTIC AGENTS MONDOBIOTECH LABORATORIES AG (LI) 2009-03-19 — — WO disclosed
WO-2009033667-A2 USE OF A PEPTIDE AS A THERAPEUTIC AGENT MONDOBIOTECH LABORATORIES AG (LI) 2009-03-19 — — WO disclosed
WO-2008112156-A1 CHEMOKINE RECEPTOR MODULATORS ALTIRIS THERAPEUTICS (US) 2008-09-18 — — WO disclosed
WO-2008109154-A1 CHEMOKINE RECEPTOR MODULATORS ALTIRIS THERAPEUTICS, INC. (US) 2008-09-12 — — WO disclosed
WO-2007010266-A1 PYRROLIDINE COMPOSITIONS MNL PHARMA LIMITED (GB) 2007-01-25 — — WO disclosed
WO-2006129134-A1 SYNERGIC COMBINATIONS COMPRISING A STYRYLQUINOLINE COMPOUND AND OTHER HIV INFECTION THERAPEUTIC AGENTS BIOALLIANCE PHARMA (FR) 2006-12-07 — — WO disclosed
US-7135467-B2 Pyrimidine carboxamides; 5-hydroxy-2-(2-(1,1-Dioxo-6-[1,2]thiazinan-2-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamides; AIDS; AIDS related complex BRISTOL-MYERS SQUIBB COMPANY (US) 2006-11-14 — — US disclosed
WO-2006077427-A2 ANTIVIRAL DRUG COMBINATIONS MNL PHARMA LIMITED (GB) 2006-07-27 — — WO disclosed
US-20040204498-A1 HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-10-14 — — US disclosed
WO-2004062613-A2 HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2004-07-29 — — WO 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 (2 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-20040204498-A1 HIV integrase inhibitors IMPDH1, TYMP, REV1 UGT1A1 319/4885MLNR 3936/4885NR1I2 838/4885
US-20160038502-A1 HIV TREATMENT FORMULATION OF ATAZANAVIR AND COBICISTAT APOBEC3A, SAMHD1, ADA UGT1A1 1305/4885MLNR 3972/4885NR1I2 3781/4885

“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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