Pyridine

Pyridine

SCHEMBL20972307

CC.O=S(=O)(O)O.c1ccncc1

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CALCRLCHRM1CHRM2CHRM3F2RMAOAMAOBMAP2K1MAP2K2NTRK1NTRK2NTRK3OPRD1OPRK1OPRM1P2RY12PKLRSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASLC18A2SLC6A2SLC6A3TLR7TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8dacAdacBdacCfolAftsImrcAmrcBmrdApolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmB1rpmB2rpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmHrpmIrpmJrpmJ2rpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsR1rpsR2rpsSrpsTrpsUrpsZykgMykgO

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 17)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 3/20 0.53
TSHR P16473 2/20 0.53
TDP1 Q9NUW8 2/20 0.53
CA5A P35218 1/20 0.35
CA5B Q9Y2D0 1/20 0.35
HPGD P15428 1/20 0.34
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
ALDH1A1 P00352 1/20 0.31
APP P05067 1/20 0.31
GAA P10253 1/20 0.31
HCAR3 P49019 1/20 0.31
HCAR2 Q8TDS4 1/20 0.31
LMNA P02545 1/20 0.31
KDM4E B2RXH2 1/20 0.30
ALOX12 P18054 1/20 0.30

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
Pyridine SCHEMBL20972306 1.00 NAPRT (0.53) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL22261964 0.94 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL1407986 0.94 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL3316655 0.94 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL407438 0.94 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL22261990 0.94 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL1005857 0.94 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL25405557 0.91 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL122022 0.91 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL22151316 0.91 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190148754-A1 USE OF IONIC LIQUIDS AS AN ADJUVANT IN ELECTROCHEMISTRY UNIVERSITE DE RENNES 1 (FR) 2019-05-16 US claimed
CN-109643817-A Use of ionic liquids as adjuvants in electrochemistry 雷恩第大学 2019-04-16 CN claimed
US-20190148754-A1 USE OF IONIC LIQUIDS AS AN ADJUVANT IN ELECTROCHEMISTRY UNIVERSITE DE RENNES 1 (FR) 2019-05-16 US disclosed
CN-109643817-A Use of ionic liquids as adjuvants in electrochemistry 雷恩第大学 2019-04-16 CN disclosed