Tipranavir

Tipranavir

SCHEMBL13536854

CCC[C@@]1(CCc2ccccc2)CC(O)=C(C(CC)c2cccc(NS(=O)(=O)c3ccc(C(F)(F)F)cn3)c2)C(=O)O1

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 Tipranavir. 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
▸ MLNR O43193 1/20 1.00
▸ NR1I2 O75469 1/20 1.00
▸ ABCB11 O95342 1/20 1.00
▸ PGR P06401 1/20 1.00
▸ CTSD P07339 1/20 1.00
▸ CHRM2 P08172 1/20 1.00
▸ ADRA2A P08913 1/20 1.00
▸ PGA5 P0DJD9 1/20 1.00
▸ ADORA3 P0DMS8 1/20 1.00
▸ CTSE P14091 1/20 1.00
▸ GABRA1 P14867 1/20 1.00
▸ ADRA2C P18825 1/20 1.00
▸ DRD1 P21728 1/20 1.00
▸ HTR2A P28223 1/20 1.00
▸ AGTR1 P30556 1/20 1.00
▸ CCKAR P32238 1/20 1.00
▸ ADRA1A P35348 1/20 1.00
▸ PTGS2 P35354 1/20 1.00
▸ PPARG P37231 1/20 1.00
▸ OPRD1 P41143 1/20 1.00

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
Tipranavir SCHEMBL6957763 1.00 MLNR (1.00) MLNRNR1I2ABCB11PGRCTSD
Tipranavir SCHEMBL5414762 1.00 MLNR (1.00) MLNRNR1I2ABCB11PGRCTSD
Tipranavir SCHEMBL6953675 1.00 MLNR (1.00) MLNRNR1I2ABCB11PGRCTSD
Tipranavir SCHEMBL40629 1.00 MLNR (1.00) MLNRNR1I2ABCB11PGRCTSD
Tipranavir SCHEMBL29393318 1.00 MLNR (1.00) MLNRNR1I2ABCB11PGRCTSD
Tipranavir SCHEMBL7407890 1.00 MLNR (1.00) MLNRNR1I2ABCB11PGRCTSD
Tipranavir SCHEMBL434955 0.99 MLNR (0.99) MLNRNR1I2ABCB11PGRCTSD
SCHEMBL7398499 0.98 MLNR (0.96) MLNRNR1I2ABCB11PGRCTSD
SCHEMBL7398500 0.98 MLNR (0.96) MLNRNR1I2ABCB11PGRCTSD
SCHEMBL7401866 0.98 MLNR (0.96) MLNRNR1I2ABCB11PGRCTSD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210246125-A1 PYRANONE COMPOUNDS USEFUL TO MODULATE OMA1 PROTEASE 712 NORTH INC. 2021-08-12 — — US claimed
US-20240041764-A1 Sustained-Release Oral Fosamprenavir Formulation for Treatment of Reflux N-ZYME BIOMEDICAL INC. (CA) 2024-02-08 — — US disclosed
US-20230172846-A1 ORAL DISSOLVABLE FILM AND METHOD OF MANUFACTURING AND USING THE SAME CUREX PHARMACEUTICAL MEXICO S.A.P.I. DE C.V. (MX) 2023-06-08 — — US disclosed
US-20230078695-A1 Aerosolized Formulations of HIV Protease Inhibitors for the Treatment of Airway Reflux THE MEDICAL COLLEGE OF WISCONSIN, INC. 2023-03-16 — — US disclosed
US-20180221406-A1 THERAPEUTIC COMBINATIONS OF ANTIVIRAL AND ANTI-INFLAMMATORY THERAPIES FORESIGHT BIOTHERAPEUTICS, INC. (US) 2018-08-09 — — US disclosed
EP-2752422-B1 Stereoselective synthesis of phosphorus containing actives GILEAD PHARMASSET LLC (US) 2017-08-16 — — EP disclosed
US-20110245484-A1 STEREOSELECTIVE SYNTHESIS OF PHOSPHORUS CONTAINING ACTIVES PHARMASSET, INC. (US) 2011-10-06 — — US disclosed
US-7649015-B2 Cellular accumulation of phosphonate analogs of HIV protease inhibitor compounds GILEAD SCIENCES, INC. (US) 2010-01-19 — — US disclosed
US-7649015-B2 Cellular accumulation of phosphonate analogs of HIV protease inhibitor compounds GILEAD SCIENCES, INC. (US) 2010-01-19 — — US disclosed
US-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds GILEAD SCIENCES, INC. 2007-01-11 — — 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 (5 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-20180221406-A1 THERAPEUTIC COMBINATIONS OF ANTIVIRAL AND ANTI-INFLAMMATORY THERAPIES EIF2AK2, IRF3, IFNG MLNR 4370/4885NR1I2 727/4885ABCB11 3192/4885
US-20210246125-A1 PYRANONE COMPOUNDS USEFUL TO MODULATE OMA1 PROTEASE OPA1, OLA1, PITRM1 MLNR 4622/4885NR1I2 2201/4885ABCB11 3758/4885
US-20110245484-A1 STEREOSELECTIVE SYNTHESIS OF PHOSPHORUS CONTAINING ACTIVES PPA1, ENPP1, ITPA MLNR 3396/4885NR1I2 3329/4885ABCB11 2686/4885
US-20230172846-A1 ORAL DISSOLVABLE FILM AND METHOD OF MANUFACTURING AND USING THE SAME DSTN, FDFT1, DDHD2 MLNR 3066/4885NR1I2 3489/4885ABCB11 1183/4885
US-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds PPA1, PNP, PPME1 MLNR 4092/4885NR1I2 4255/4885ABCB11 2761/4885

“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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