Pyridine

Pyridine

SCHEMBL28404147

Cl.O=C(O)C(c1cccs1)c1cccs1.c1ccncc1.c1ccncc1

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
CHRM2 known ✓ P08172 1/20 0.37
CHRM1 known ✓ P11229 1/20 0.37
CHRM3 known ✓ P20309 1/20 0.37
TSHR P16473 1/20 0.46
CES2 O00748 2/20 0.42
CES1 P23141 2/20 0.42
KEAP1 Q14145 1/20 0.42
CYP2C19 P33261 1/20 0.41
ALDH1A1 P00352 4/20 0.40
HTT P42858 2/20 0.40
MAPT P10636 2/20 0.40
NPSR1 Q6W5P4 2/20 0.40
PKM P14618 1/20 0.40
HPGD P15428 1/20 0.40
ATM Q13315 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
ALOX5 P09917 1/20 0.39
DAO P14920 1/20 0.38
AHR P35869 1/20 0.38
LMNA P02545 2/20 0.36

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 SCHEMBL29016896 1.00 TSHR (0.46) TSHRCES2CES1KEAP1CYP2C19
Pyridine SCHEMBL30437342 0.98 TSHR (0.47) TSHRCES2CES1KEAP1CYP2C19
SCHEMBL72374 0.89 CES2 (0.50) TSHRCES2CES1KEAP1CYP2C19
Fluoride SCHEMBL14931714 0.87 CES2 (0.48) TSHRCES2CES1KEAP1CYP2C19
Fluoride SCHEMBL14774852 0.87 CES2 (0.48) TSHRCES2CES1KEAP1CYP2C19
Fumaric Acid SCHEMBL28542597 0.80 HCAR2 (0.50) TSHRCES2CES1KEAP1CYP2C19
SCHEMBL4619853 0.78 POLB (0.50) TSHRCES2CES1KEAP1CYP2C19
Hydrochloric Acid SCHEMBL3891233 0.76 ALOX5 (0.46) CES2CES1KEAP1CYP2C19ALDH1A1
SCHEMBL11078590 0.74 MAPT (0.39) TSHRCES2CES1KEAP1CYP2C19
SCHEMBL891673 0.73 ALOX5 (0.47) CES2CES1KEAP1CYP2C19ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116102691-B Viscosity-reducing water reducer for high-strength concrete and preparation method thereof 石家庄市长安育才建材有限公司 2023-08-08 CN claimed
CN-116283030-B Early-strength viscosity-reducing water reducer and preparation method thereof 石家庄市长安育才建材有限公司 2023-08-08 CN claimed
CN-116283030-A Early-strength viscosity-reducing water reducer and preparation method thereof 石家庄市长安育才建材有限公司 2023-06-23 CN claimed
CN-116102691-A Viscosity-reducing water reducer for high-strength concrete and preparation method thereof 石家庄市长安育才建材有限公司 2023-05-12 CN claimed
CN-111217966-A Viscosity-reducing early-strength concrete water reducer and preparation method thereof 刘翠芬 2020-06-02 CN claimed
CN-116102691-B Viscosity-reducing water reducer for high-strength concrete and preparation method thereof 石家庄市长安育才建材有限公司 2023-08-08 CN disclosed
CN-116283030-B Early-strength viscosity-reducing water reducer and preparation method thereof 石家庄市长安育才建材有限公司 2023-08-08 CN disclosed
CN-116283030-A Early-strength viscosity-reducing water reducer and preparation method thereof 石家庄市长安育才建材有限公司 2023-06-23 CN disclosed
CN-116102691-A Viscosity-reducing water reducer for high-strength concrete and preparation method thereof 石家庄市长安育才建材有限公司 2023-05-12 CN disclosed
CN-111217966-A Viscosity-reducing early-strength concrete water reducer and preparation method thereof 刘翠芬 2020-06-02 CN disclosed