Pyridine

Pyridine

SCHEMBL10980010

CC(=O)NN.Cl.c1ccncc1

nearest known ligand 0.43

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
NAPRT Q6XQN6 2/20 0.43
TSHR P16473 2/20 0.43
TDP1 Q9NUW8 1/20 0.43
CYP1A2 P05177 3/20 0.40
CYP3A4 P08684 3/20 0.40
CYP2D6 P10635 2/20 0.40
CYP2C19 P33261 2/20 0.40
KDM4E B2RXH2 1/20 0.40
MPO P05164 1/20 0.40
ADORA3 P0DMS8 1/20 0.40
CYP2A6 P11509 1/20 0.40
P2RX7 Q99572 3/20 0.37
TP53 P04637 1/20 0.36
CYP2C9 P11712 2/20 0.36
ALDH1A1 P00352 2/20 0.33
TAAR1 Q96RJ0 1/20 0.33
PLOD2 O00469 1/20 0.33
PLOD3 O60568 1/20 0.33
HPGD P15428 1/20 0.33
PLOD1 Q02809 1/20 0.33

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 SCHEMBL10974779 0.98 NAPRT (0.45) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL294375 0.82 NAPRT (0.50) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL27295109 0.82 NAPRT (0.50) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL9134951 0.82 NAPRT (0.50) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL9073450 0.82 NAPRT (0.56) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL11225938 0.82 NAPRT (0.56) NAPRTTSHRTDP1CYP1A2CYP3A4
Benzene SCHEMBL5880091 0.82 NAPRT (0.43) NAPRTTSHRCYP1A2CYP3A4KDM4E
Pyridine SCHEMBL4655282 0.80 TDP1 (0.47) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL27474885 0.80 CYP1A2 (0.53) NAPRTTSHRTDP1CYP1A2CYP3A4
Pyridine SCHEMBL4528020 0.79 NAPRT (0.53) NAPRTTSHRTDP1CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113880905-A Progesterone refining method 浙江神洲药业有限公司 2022-01-04 CN claimed
CN-111269102-A Method for extracting phorbol from croton oil by using Giralde reagent 南昌大学 2020-06-12 CN claimed
CN-113880905-A Progesterone refining method 浙江神洲药业有限公司 2022-01-04 CN disclosed
CN-111269102-A Method for extracting phorbol from croton oil by using Giralde reagent 南昌大学 2020-06-12 CN disclosed
EP-0056692-B1 7-SUBSTITUTED CAMPTOTHECIN DERIVATIVES AND PROCESS FOR THEIR PREPARATION KABUSHIKI KAISHA YAKULT HONSHA (JP) 1985-08-14 EP disclosed
EP-0089394-A1 1-H-Indole-2,3-dione derivatives and preparation thereof STERLING DRUG INC. (US) 1983-09-28 EP disclosed
US-4399276-A 7-Substituted camptothecin derivatives KABUSHIKI KAISHA YAKULT HONSHA (JP) 1983-08-16 US disclosed
US-4382941-A BACTERICIDES; FUNGICIDES; MICROBIOCIDES; CATIONIC SURFACTANTS SICARDI SUSANA M 1983-05-10 US disclosed
EP-0056692-A1 7-Substituted camptothecin derivatives and process for their preparation KABUSHIKI KAISHA YAKULT HONSHA (JP) 1982-07-28 EP disclosed
US-4322533-A CARDIOTONIC, BRONCHODILATOR, AND ANTICHLOLINERGIC AGENTS; ANTIMISTAMINES; ANTIALLERGENS STERLING DRUG INC. 1982-03-30 US disclosed
US-4267094-A COMPRISING AN ACRYLIC-VINYLIDENE HALIDE POLYMER AND AN ACRYLAMIDE POLYMER BAYER AKTIENGESELLSCHAFT (DE) 1981-05-12 US disclosed
US-4065455-A REAGENTS FOR ION EXCHANGE EXTRACTION OF METALS GENERAL MILLS CHEMICALS, INC. (US) 1977-12-27 US disclosed
US-4051223-A SELECTIVE, CALCIUM SEPARATION, HYDROGEN ION EXCHANGE RESIN GENERAL MILLS CHEMICALS, INC. (US) 1977-09-27 US disclosed