Oxypertine

Oxypertine

SCHEMBL2837214

COc1cc2[nH]c(C)c(CCN3CCN(c4ccccc4)CC3)c2cc1OC.c1ccc(-c2ccccc2)cc1

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ DRD2 P14416 5/20 0.94
▸ HTR1A P08908 3/20 0.94
▸ HTR2A P28223 2/20 0.94
▸ NR1I2 O75469 1/20 0.94
▸ ADRB1 P08588 1/20 0.94
▸ ADRA2A P08913 1/20 0.94
▸ ADORA3 P0DMS8 1/20 0.94
▸ ADRA2B P18089 1/20 0.94
▸ ADRA2C P18825 1/20 0.94
▸ SLC6A2 P23975 1/20 0.94
▸ HTR2C P28335 1/20 0.94
▸ PTGS2 P35354 1/20 0.94
▸ HRH1 P35367 1/20 0.94
▸ HTR2B P41595 1/20 0.94
▸ CHRNA4 P43681 1/20 0.94
▸ SLC6A3 Q01959 1/20 0.94
▸ PDE4D Q08499 1/20 0.94
▸ KCNH2 Q12809 1/20 0.94
▸ HTR7 P34969 1/20 0.47
▸ MAPT P10636 4/20 0.44

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
Oxypertine SCHEMBL1515 0.97 DRD2 (1.00) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL2463001 0.97 DRD2 (1.00) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL31153315 0.97 DRD2 (1.00) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL5069690 0.96 DRD2 (0.98) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL3478579 0.96 DRD2 (0.98) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL20270862 0.96 DRD2 (0.98) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL3440995 0.96 DRD2 (0.98) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL21268763 0.94 HTR1A (0.94) DRD2HTR1AHTR2ANR1I2ADRB1
Oxypertine SCHEMBL7527152 0.91 HTR1A (0.88) DRD2HTR1AHTR2ANR1I2ADRB1
SCHEMBL2615395 0.89 DRD2 (0.84) DRD2HTR1AHTR2ANR1I2ADRB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180344803-A1 Methods and Compositions For the Treatment of Proteinuric Diseases THE GENERAL HOSPITAL CORPORATION 2018-12-06 — — US disclosed
US-20160296592-A1 Methods and Compositions for the Treatment of Proteinuric Diseases THE GENERAL HOSPITAL CORPORATION 2016-10-13 — — US disclosed
US-9345739-B2 Methods and compositions for the treatment of proteinuric diseases THE GENERAL HOSPITAL CORPORATION (US) 2016-05-24 — — US disclosed
EP-2730282-A1 Methods and compositions for the treatment of proteinuric diseases The General Hospital Corporation (US) 2014-05-14 — — EP disclosed
US-20100297139-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF PROTEINURIC DISEASES THE GENERAL HOSPITAL CORPORATION 2010-11-25 — — US disclosed
EP-2217238-A2 METHODS AND COMPOSITIONS FOR THE TREATMENT OF PROTEINURIC DISEASES The General Hospital Corporation (US) 2010-08-18 — — EP disclosed
WO-2009061448-A9 METHODS AND COMPOSITIONS FOR THE TREATMENT OF PROTEINURIC DISEASES THE GENERAL HOSPITAL CORPORATION (US) 2009-08-13 — — WO disclosed
WO-2009061448-A2 METHODS AND COMPOSITIONS FOR THE TREATMENT OF PROTEINURIC DISEASES THE GENERAL HOSPITAL CORPORATION (US) 2009-05-14 — — WO disclosed
US-20080064716-A1 Alpha v beta 3 and/or alpha v beta 5 integrin inhibitors; osteoporosis, retinopathy, tumor metastasis and angiogenesis; decreased side effects, improved potency; 3-(2-(3-[2-(5,6,7,8- Tetrahydro-1,8-naphthyridin-2-yl)ethoxy]benzyl}-phenyl)propionic acid PHARMACIA 2008-03-13 — — US disclosed
US-20080064716-A1 Alpha v beta 3 and/or alpha v beta 5 integrin inhibitors; osteoporosis, retinopathy, tumor metastasis and angiogenesis; decreased side effects, improved potency; 3-(2-(3-[2-(5,6,7,8- Tetrahydro-1,8-naphthyridin-2-yl)ethoxy]benzyl}-phenyl)propionic acid PHARMACIA 2008-03-13 — — US disclosed
EP-1802618-A1 BIPHENYL INTEGRIN ANTAGONISTS Pharmacia Corporation (US) 2007-07-04 — — EP disclosed
EP-1802618-A1 BIPHENYL INTEGRIN ANTAGONISTS Pharmacia Corporation (US) 2007-07-04 — — EP disclosed
WO-2006043930-A1 BIPHENYL INTEGRIN ANTAGONISTS PHARMACIA CORPORATION (US) 2006-04-27 — — WO disclosed
WO-2006043930-A1 BIPHENYL INTEGRIN ANTAGONISTS PHARMACIA CORPORATION (US) 2006-04-27 — — 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 (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-20160296592-A1 Methods and Compositions for the Treatment of Proteinuric Diseases ITGB3, PLAUR, PROC DRD2 4797/4885HTR1A 4517/4885HTR2A 4073/4885
US-20080064716-A1 Alpha v beta 3 and/or alpha v beta 5 integrin inhibitors; osteoporosis, retinopathy, tumor metastasis and angiogenesis; decreased side effects, improved potency; 3-(2-(3-[2-(5,6,7,8- Tetrahydro-1,8-naphthyridin-2-yl)ethoxy]benzyl}-phenyl)propionic acid ITGA5, ITGAV, ITGB5 DRD2 2127/4885HTR1A 2510/4885HTR2A 3876/4885
US-20180344803-A1 Methods and Compositions For the Treatment of Proteinuric Diseases ITGB3, PLAUR, PROC DRD2 4797/4885HTR1A 4517/4885HTR2A 4073/4885
US-20100297139-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF PROTEINURIC DISEASES ITGB3, PLAUR, PROC DRD2 4797/4885HTR1A 4517/4885HTR2A 4073/4885

“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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