Sorbinil

Sorbinil

SCHEMBL2108408

O=C1NC(=O)C2(CCOc3ccc(F)cc32)N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AKR1B1

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
AKR1B1 known ✓ P15121 1/20 1.00
AKR1B10 O60218 1/20 1.00
MAPT P10636 1/20 1.00
AKR1A1 P14550 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
Sorbinil SCHEMBL17223865 1.00 AKR1B10 (1.00) AKR1B10MAPTAKR1A1AKR1B1
Sorbinil SCHEMBL9790028 1.00 AKR1B10 (1.00) AKR1B10MAPTAKR1A1AKR1B1
Sorbinil SCHEMBL29599732 1.00 AKR1B10 (1.00) AKR1B10MAPTAKR1A1AKR1B1
Sorbinil SCHEMBL48877 1.00 AKR1B10 (1.00) AKR1B10MAPTAKR1A1AKR1B1
SCHEMBL12620675 0.89 AKR1B10 (0.80) AKR1B10MAPTAKR1A1AKR1B1
SCHEMBL7867894 0.89 AKR1B10 (0.80) AKR1B10MAPTAKR1A1AKR1B1
Sorbinil SCHEMBL11088391 0.88 AKR1B10 (0.78) AKR1B10MAPTAKR1A1AKR1B1
Sorbinil SCHEMBL11097273 0.88 AKR1B1 (0.78) AKR1B10MAPTAKR1A1AKR1B1
SCHEMBL3439473 0.86 AKR1B1 (0.76) AKR1B10MAPTAKR1A1AKR1B1
SCHEMBL9824214 0.86 AKR1B1 (0.76) AKR1B10MAPTAKR1A1AKR1B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0111387-B1 REGENERATION OF 6-FLUORO-4-CHROMANONE FROM BY-PRODUCTS IN THE SYNTHESIS OF SORBINIL PFIZER INC. (US) 1986-04-09 EP claimed
EP-0175312-A2 Process for preparing optically active hydantoins KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1986-03-26 EP claimed
EP-0111387-A1 Regeneration of 6-fluoro-4-chromanone from by-products in the synthesis of sorbinil PFIZER INC. (US) 1984-06-20 EP claimed
US-4431828-A Regeneration of 6-fluoro-4-chromanone from by-products in the synthesis of sorbinil PFIZER INC. (US) 1984-02-14 US claimed
US-4177282-A ANITDIABETIC PFIZER INC. (US) 1979-12-04 US claimed
US-4147795-A ENZYME INHIBITORS PFIZER INC. (US) 1979-04-03 US claimed
US-4130714-A SPIRO CHROMANS OR THIOCHROMANS PFIZER INC. (US) 1978-12-19 US claimed
US-20140349969-A1 COMPOUNDS AND METHODS FOR TREATING PAIN AKRON MOLECULES AG (AT) 2014-11-27 US disclosed
EP-2674161-A1 FMO3 inhibitors for treating pain Akron Molecules GmbH (AT) 2013-12-18 EP disclosed
US-20130252924-A1 Compounds and Methods for Treating Pain AKRON MOLECULES GMBH (AT) 2013-09-26 US disclosed
US-8158667-B2 Topical treatment of cataracts in dogs BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA 2012-04-17 US disclosed
WO-2010065024-A1 TOPICAL TREATMENT OF CATARACTS IN DOGS KADOR PETER F (US) 2010-06-10 WO disclosed
US-20090082415-A1 Topical treatment of cataracts in dogs BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA 2009-03-26 US disclosed
US-4177282-A ANITDIABETIC PFIZER INC. (US) 1979-12-04 US disclosed
US-4147795-A ENZYME INHIBITORS PFIZER INC. (US) 1979-04-03 US disclosed
US-4147795-A ENZYME INHIBITORS PFIZER INC. (US) 1979-04-03 US disclosed
US-4130714-A SPIRO CHROMANS OR THIOCHROMANS PFIZER INC. (US) 1978-12-19 US disclosed
US-4130714-A SPIRO CHROMANS OR THIOCHROMANS PFIZER INC. (US) 1978-12-19 US disclosed
US-4117230-A ANTIDIABETIC AGENTS PFIZER INC. (US) 1978-09-26 US disclosed
US-4117230-A ANTIDIABETIC AGENTS PFIZER INC. (US) 1978-09-26 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 (3 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-20140349969-A1 COMPOUNDS AND METHODS FOR TREATING PAIN TRPV1, ACHE, OPRL1 AKR1B1 1566/4885AKR1B10 1719/4885MAPT 898/4885
US-20090082415-A1 Topical treatment of cataracts in dogs AKR1A1, AKR1B1, AKR1C1 AKR1B1 2/4885AKR1B10 9/4885MAPT 758/4885
US-20130252924-A1 Compounds and Methods for Treating Pain TRPV1, ACHE, OPRL1 AKR1B1 1566/4885AKR1B10 1719/4885MAPT 898/4885

“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.