Pyridine

Pyridine

SCHEMBL2993097

CC(=O)O.CCCCO.CCO.O.c1ccncc1

nearest known ligand 0.42

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
ALDH1A1 P00352 3/20 0.42
SMN1; SMN2 Q16637 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.35
TSHR P16473 3/20 0.35
NAPRT Q6XQN6 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
LMNA P02545 6/20 0.34
HSD17B10 Q99714 1/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
CES1 P23141 1/20 0.34
HDAC3 O15379 2/20 0.33
HDAC1 Q13547 2/20 0.33
HDAC2 Q92769 2/20 0.33
POLB P06746 1/20 0.33
NAAA Q02083 1/20 0.33
HTT P42858 1/20 0.32
CYP1A2 P05177 1/20 0.32
CYP2C9 P11712 1/20 0.32
CYP2C19 P33261 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
Pyridine SCHEMBL907254 0.98 ALDH1A1 (0.44) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL7422031 0.96 ALDH1A1 (0.46) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL618965 0.90 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Benzene SCHEMBL6273750 0.90 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL9766208 0.88 NAPRT (0.41) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL10539991 0.88 ALDH1A1 (0.50) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL1460187 0.88 ALDH1A1 (0.55) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL12476946 0.88 ALDH1A1 (0.55) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL1079036 0.86 NAPRT (0.43) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT
Pyridine SCHEMBL11779483 0.86 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2L3MBTL1TSHRNAPRT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10919941-B2 Functional lipid constructs KODE BIOTECH LIMITED (NZ) 2021-02-16 US disclosed
US-10858384-B2 Synthetic molecule constructs KODE BIOTECH LIMITED (NZ) 2020-12-08 US disclosed
US-20200123188-A1 SYNTHETIC MOLECULE CONSTRUCTS KODE BIOTECH LIMITED (NZ) 2020-04-23 US disclosed
US-10414786-B2 Synthetic membrane anchors KODE BIOTECH LIMITED (NZ) 2019-09-17 US disclosed
US-20180057518-A1 SYNTHETIC MEMBRANE ANCHORS KODE BIOTECH LTD. (NZ) 2018-03-01 US disclosed
US-20170218027-A1 FUNCTIONAL LIPID CONSTRUCTS KODE BIOTECH LIMITED (NZ) 2017-08-03 US disclosed
US-20160361423-A1 CARBOHYDRATE-LIPID CONSTRUCTS AND THEIR USE IN PREVENTING OR TREATING VIRAL INFECTION KODE BIOTECH LTD (NZ) 2016-12-15 US disclosed
US-9226968-B2 Carbohydrate-lipid constructs and their use in preventing or treating viral infection KODE BIOTECH LIMITED (NZ) 2016-01-05 US disclosed
US-20140200191-A1 CARBOHYDRATE-LIPID CONSTRUCTS AND THEIR USE IN PREVENTING OR TREATING VIRAL INFECTION KODE BIOTECH LIMITED (NZ) 2014-07-17 US disclosed
US-20120277172-A1 CARBOHYDRATE-LIPID CONSTRUCTS AND THEIR USE IN PREVENTING OR TREATING VIRAL INFECTION KODE BIOTECH LIMITED (NZ) 2012-11-01 US disclosed
US-6706497-B2 GENERATION OF SIALYLOLIGOSACCHARIDES IN A DAIRY PRODUCTS; OBTAIN ENZYME MIXTURE, INCUBATE WITH MILK, RECOVER SIALYLOLIGOSACCHARIDES NEOSE TECHNOLOGIES, INC. 2004-03-16 US disclosed
US-20020150995-A1 Methods for producing sialyloligosaccharides in a dairy source NEOSE TECHNOLOGIES, INC. 2002-10-17 US disclosed
US-6323008-B1 CONTACTING .ALPHA.(2,3)TRANS-SIALIDASE WITH DAIRY SOURCE COMPRISING LACTOSE AND SIALIC ACID DONORS TO FORM DAIRY/TRANS-SIALIDASE MIXTURE; INCUBATING TO EFFECT TRANSFER OF SIALIC ACID FROM SIALIC ACID DONORS TO LACTOSE NEOSE TECHNOLOGIES, INC. 2001-11-27 US disclosed
US-6218161-B1 DNA ENCODING AN ACTIVE DOMAIN OF N-ACETYLGALACTOSAMINE-ALPHA-2,6-SIALYLTRANSFERASE; FOR RECOMBINANT PRODUCTION THE INSTITUTE OF PHYSICAL AND CHEMICAL RESEARCH (JP) 2001-04-17 US disclosed
EP-1003366-A1 METHODS FOR PRODUCING SIALYLOLIGOSACCHARIDES IN A DAIRY SOURCE Neose Technologies, Inc. (US) 2000-05-31 EP disclosed
WO-1999008511-A1 METHODS FOR PRODUCING SIALYLOLIGOSACCHARIDES IN A DAIRY SOURCE NEOSE TECHNOLOGIES, INC. (US) 1999-02-25 WO disclosed
EP-0737745-A1 NOVEL SUGAR-CHAIN SYNTHETASE AND PROCESS FOR PRODUCING THE SAME THE INSTITUTE OF PHYSICAL & CHEMICAL RESEARCH (JP) 1996-10-16 EP disclosed
EP-0586687-A4 TRANS-SIALIDASE AND METHODS OF USE AND MAKING THEREOF UNIV NEW YORK (US) 1996-04-17 EP disclosed
EP-0586687-A1 TRANS-SIALIDASE AND METHODS OF USE AND MAKING THEREOF NEW YORK UNIVERSITY (US) 1994-03-16 EP disclosed
WO-1993018787-A1 TRANS-SIALIDASE AND METHODS OF USE AND MAKING THEREOF NEW YORK UNIVERSITY (US) 1993-09-30 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 (9 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-20140200191-A1 CARBOHYDRATE-LIPID CONSTRUCTS AND THEIR USE IN PREVENTING OR TREATING VIRAL INFECTION HAVCR2, SIGLEC7, FUT5 ALDH1A1 3182/4885SMN1; SMN2 4767/4885L3MBTL1 1442/4885
US-20160361423-A1 CARBOHYDRATE-LIPID CONSTRUCTS AND THEIR USE IN PREVENTING OR TREATING VIRAL INFECTION HAVCR2, SIGLEC7, FUT5 ALDH1A1 3182/4885SMN1; SMN2 4767/4885L3MBTL1 1442/4885
US-20170218027-A1 FUNCTIONAL LIPID CONSTRUCTS CETP, LCAT, LIPA ALDH1A1 1782/4885SMN1; SMN2 4732/4885L3MBTL1 1458/4885
US-10919941-B2 Functional lipid constructs CETP, LCAT, LIPA ALDH1A1 1782/4885SMN1; SMN2 4732/4885L3MBTL1 1458/4885
US-20180057518-A1 SYNTHETIC MEMBRANE ANCHORS PTDSS2, DDOST, STT3B ALDH1A1 3805/4885SMN1; SMN2 4788/4885L3MBTL1 149/4885
US-20200123188-A1 SYNTHETIC MOLECULE CONSTRUCTS PTDSS2, PTDSS1, UGCG ALDH1A1 1208/4885SMN1; SMN2 4803/4885L3MBTL1 465/4885
US-20120277172-A1 CARBOHYDRATE-LIPID CONSTRUCTS AND THEIR USE IN PREVENTING OR TREATING VIRAL INFECTION HAVCR2, SIGLEC7, FUT5 ALDH1A1 3182/4885SMN1; SMN2 4767/4885L3MBTL1 1442/4885
US-10414786-B2 Synthetic membrane anchors PTDSS2, DDOST, STT3B ALDH1A1 3838/4885SMN1; SMN2 4783/4885L3MBTL1 157/4885
US-10858384-B2 Synthetic molecule constructs PTDSS2, PTDSS1, UGCG ALDH1A1 1238/4885SMN1; SMN2 4797/4885L3MBTL1 474/4885

“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.