Pyridine

Pyridine

SCHEMBL3316655

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

nearest known ligand 0.60

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 20)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 4/20 0.60
TSHR P16473 2/20 0.60
TDP1 Q9NUW8 1/20 0.60
CA5A P35218 1/20 0.40
CA5B Q9Y2D0 1/20 0.40
SMN1; SMN2 Q16637 2/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35
GAA P10253 2/20 0.33
ALDH1A1 P00352 2/20 0.33
APP P05067 1/20 0.33
HCAR3 P49019 1/20 0.33
HCAR2 Q8TDS4 1/20 0.33
HPGD P15428 3/20 0.32
KDM4E B2RXH2 2/20 0.32
ALOX12 P18054 1/20 0.32
TAAR1 Q96RJ0 1/20 0.31
PLOD2 O00469 1/20 0.31
PLOD3 O60568 1/20 0.31
CYP1A2 P05177 1/20 0.31

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 SCHEMBL22261990 1.00 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL1005857 1.00 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL22261964 1.00 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL1407986 1.00 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL407438 1.00 NAPRT (0.60) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL25405557 0.97 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL22151317 0.97 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL22151316 0.97 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL122022 0.97 NAPRT (0.56) NAPRTTSHRTDP1CA5ACA5B
Pyridine SCHEMBL11617873 0.97 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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8324179-B2 Nucleoside analogs for antiviral treatment GILEAD SCIENCES, INC. (US) 2012-12-04 US disclosed
US-20100104532-A1 NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES, INC. (US) 2010-04-29 US disclosed
WO-2008100447-A2 NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES, INC. (US) 2008-08-21 WO disclosed
US-6617306-B2 Therapeutic agent is conjugated to the carrier via a biodegradable disulfide bond. RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY 2003-09-09 US disclosed
US-20020058611-A1 Carrier for in vivo delivery of a therapeutic agent RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY 2002-05-16 US disclosed
US-6258774-B1 A POLYMER, MULTIPLE THIOL COMPOUNDS CONJUGATED TO THE POLYMER FORMING A DISULFIDE BOND, A CELL UPTAKE PROMOTER CONJUGATED TO THE POLYMER; PROTECTED FROM DEGRADATION AND RENAL CLEARANCE, IMMUNE RESPONSE IS LIMITED UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY 2001-07-10 US disclosed
EP-1082139-A2 CARRIER FOR $i(IN VIVO) DELIVERY OF A THERAPEUTIC AGENT UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY (US) 2001-03-14 EP disclosed
WO-1999047173-A2 CARRIER FOR IN VIVO DELIVERY OF A THERAPEUTIC AGENT UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY (US) 1999-09-23 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 (1 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-20100104532-A1 NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT SLC29A1, NUDT1, EIF2AK2 NAPRT 98/4885TSHR 4612/4885TDP1 966/4885

“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.