Pyridine

Pyridine

SCHEMBL4462835

CC(=O)O.O=c1cccn[nH]1.c1ccncc1

nearest known ligand 0.37

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Pyridine. 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
HCAR2 Q8TDS4 2/20 0.37
NAMPT P43490 1/20 0.36
ALDH1A1 P00352 3/20 0.36
GAA P10253 2/20 0.36
APP P05067 1/20 0.36
HCAR3 P49019 1/20 0.36
NAPRT Q6XQN6 3/20 0.33
CYP2A6 P11509 2/20 0.33
KMT2A Q03164 2/20 0.33
KDM4E B2RXH2 1/20 0.33
CYP2E1 P05181 1/20 0.33
CYP2B6 P20813 1/20 0.33
NPC1 O15118 1/20 0.33
ALOX15 P16050 1/20 0.33
CDK2 P24941 1/20 0.33
RAB9A P51151 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
MEN1 O00255 1/20 0.33
TSHR P16473 1/20 0.32

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
Acetic Acid SCHEMBL4456446 0.93 HCAR2 (0.42) HCAR2NAMPTALDH1A1GAAAPP
Pyridine SCHEMBL27717610 0.91 TSHR (0.39) HCAR2NAMPTALDH1A1GAAAPP
Methyl Alcohol SCHEMBL27901542 0.87
Bicarbonate SCHEMBL14880924 0.85 HCAR2 (0.45) HCAR2NAMPTALDH1A1GAAAPP
Oxalic Acid SCHEMBL27558037 0.83 HCAR2 (0.43) HCAR2NAMPTALDH1A1GAAAPP
Benzene SCHEMBL27553953 0.82 CYP1A2 (0.40) HCAR2CYP2A6KMT2AKDM4ECYP2E1
Acetic Acid SCHEMBL9604109 0.81 FKBP5 (0.52) HCAR2ALDH1A1NAPRTKMT2ANPC1
SCHEMBL30564 0.80
Urea SCHEMBL5212492 0.79 HCAR2 (0.39) HCAR2NAMPTNAPRTKMT2ANPC1
Hypochlorous Acid SCHEMBL27887759 0.78

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0401981-B1 Pyridazinone deriratives PFIZER (US) 1995-04-26 EP claimed
US-7572910-B2 Pyridazinone aldose reductase inhibitors PFIZER, INC. (US) 2009-08-11 US disclosed
EP-1491541-B1 Pyridazinone aldose reductase inhibitors PFIZER PROD INC (US) 2007-01-24 EP disclosed
EP-1491540-B1 Intermediates useful for the synthesis of pyridazinone aldose reductase inhibitors PFIZER PROD INC (US) 2006-12-13 EP disclosed
EP-1236720-B1 Sulfonyl pyridazinone compounds useful as aldose reductase inhibitors PFIZER PROD INC (US) 2005-06-15 EP disclosed
US-20050113381-A1 Pyridazinone aldose reductase inhibitors MYLARI BANAVARA L (US) 2005-05-26 US disclosed
US-6872722-B2 Therapies for tissue damage resulting from ischemia PFIZER INC (US) 2005-03-29 US disclosed
EP-1260224-B1 Sulfonyl pyridazinone compounds as therapeutic agents for ischemic tissue damage PFIZER PROD INC (US) 2005-02-23 EP disclosed
US-6849629-B2 Heteroaromatic substituted sulfonyl or sulfoxide or thio-pyridazinone derivatives, useful for treating diabetic complications and cardiovascular disorders PFIZER, INC. (US) 2005-02-01 US disclosed
US-20050004124-A1 THERAPIES RELATING TO COMBINATIONS OF ALDOSE REDUCTASE INHIBITORS AND CYCLOOXYGENASE-2 INHIBITORS MYLARI BANAVARA L (US) 2005-01-06 US disclosed
EP-1260224-A1 Sulfonyl pyridazinone compounds as therapeutic agents for ischemic tissue damage Pfizer Products Inc. (US) 2002-11-27 EP disclosed
WO-2002087584-A1 COMBINATIONS OF ALDOSE REDUCTASE INHIBITORS AND CYCLOOXYGENASE-2 INHIBITORS PFIZER PRODUCTS INC. (US) 2002-11-07 WO disclosed
WO-2002079198-A1 PYRIDAZINONE ALDOSE REDUCTASE INHIBITORS PFIZER PRODUCTS INC. (US) 2002-10-10 WO disclosed
US-20020143017-A1 Pyridazinone aldose reductase inhibitors MYLARI BANAVARA L (US) 2002-10-03 US disclosed
EP-1236720-A1 Sulfonyl pyridazinone compounds useful as aldose reductase inhibitors Pfizer Products Inc. (US) 2002-09-04 EP disclosed
EP-0401981-B1 Pyridazinone deriratives PFIZER (US) 1995-04-26 EP disclosed
EP-0582643-A1 PYRIDAZINONE ACETIC ACIDS PFIZER INC. (US) 1994-02-16 EP disclosed
WO-1992017446-A2 PYRIDAZINONE ACETIC ACIDS ALDOSE REDUCTASE INHIBITORS PFIZER INC. (US) 1992-10-15 WO disclosed
US-4996204-A Antidiabetic agents PFIZER INC. (US) 1991-02-26 US disclosed
EP-0401981-A1 Pyridazinone deriratives PFIZER INC. (US) 1990-12-12 EP 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-20050113381-A1 Pyridazinone aldose reductase inhibitors SLC5A1, ALDOA, AKR1B1 HCAR2 633/4885NAMPT 230/4885ALDH1A1 30/4885
US-20020143017-A1 Pyridazinone aldose reductase inhibitors SLC5A1, AKR1B1, AKR1D1 HCAR2 610/4885NAMPT 129/4885ALDH1A1 27/4885
US-20050004124-A1 THERAPIES RELATING TO COMBINATIONS OF ALDOSE REDUCTASE INHIBITORS AND CYCLOOXYGENASE-2 INHIBITORS ALDOA, AKR1B1, ALDH2 HCAR2 597/4885NAMPT 221/4885ALDH1A1 30/4885

“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.