Pyrazine

Pyrazine

SCHEMBL8936652

CCO.CCO.c1cnccn1

nearest known ligand 0.50

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Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.50
ALDH1A1 P00352 1/20 0.50
NAPRT Q6XQN6 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
POLB P06746 1/20 0.31
NOS3 P29474 1/20 0.30
NOS1 P29475 1/20 0.30
NOS2 P35228 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
Pyrazine SCHEMBL4081041 1.00
Pyrazine SCHEMBL28899285 0.96 ALDH1A1 (0.46) TSHRALDH1A1POLB
Pyrazine SCHEMBL27594329 0.84 MAPT (0.47) TSHRALDH1A1
Pyrazine SCHEMBL28845759 0.82
Pyridine SCHEMBL8610477 0.82 TSHR (0.60) TSHRALDH1A1NAPRTTDP1
Pyridine SCHEMBL8610474 0.82 TSHR (0.60) TSHRALDH1A1NAPRTTDP1
Pyridine SCHEMBL28757618 0.82 TSHR (0.60) TSHRALDH1A1NAPRTTDP1
Pyridine SCHEMBL180736 0.82
Pyridine SCHEMBL10904050 0.79 TSHR (0.56) TSHRALDH1A1NAPRTTDP1
Pyridine SCHEMBL11518871 0.79 TSHR (0.56) TSHRALDH1A1NAPRTTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1042333-C 5, 6-disubstituted-3-picolyl ammonium halide compound and preparation method thereof AMERICAN CYANAMID CO (US) 1999-03-03 CN disclosed
CN-1190094-A Process of 5-(substituted methyl)-2,3-pyridinedicarboxylic acids AMERICAN CYANAMID CO (US) 1998-08-12 CN disclosed
US-5545835-A CHEMICAL INTERMEDIATES FOR PREPARATION OF SUBSTITUTED 2,3-PYRIDINEDICARBOXYLIC ACIDS AMERICAN CYANAMID COMPANY (US) 1996-08-13 US disclosed
US-5378843-A Halogenation, quaternization AMERICAN CYANAMID COMPANY (US) 1995-01-03 US disclosed
US-5288866-A Chemical intermediates in the preparation of purity herbicides AMERICAN CYANAMID COMPANY (US) 1994-02-22 US disclosed