Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of 2-Chloropyridine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| 2-Chloropyridine SCHEMBL932561 | 1.00 | — | — | |
| 2-Chloropyridine SCHEMBL28283275 | 0.97 | TDP1 (1.00) | — | |
| 2-Chloropyridine SCHEMBL11389784 | 0.97 | — | — | |
| 2-Chloropyridine SCHEMBL10690176 | 0.97 | TDP1 (1.00) | — | |
| 2-Chloropyridine SCHEMBL29402311 | 0.97 | — | — | |
| 2-Chloropyridine SCHEMBL16637 | 0.97 | — | — | |
| 2-Chloropyridine SCHEMBL5751999 | 0.94 | — | — | |
| 2-Chloropyridine SCHEMBL457535 | 0.94 | — | — | |
| 2-Chloropyridine SCHEMBL11437985 | 0.94 | — | — | |
| 2-Chloropyridine SCHEMBL21640063 | 0.94 | — | — |
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 148 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108341767-A | A method of preparing 2,3,5- trichloropyridines | 盐城恒盛化工有限公司 | 2018-07-31 | — | — | CN | claimed |
| CN-107501173-A | A kind of method for synthesizing 4 alkanamine yl pyridines in a mild condition | 武汉桀升生物科技有限公司 | 2017-12-22 | — | — | CN | claimed |
| WO-2017127654-A1 | METHODS FOR CATALYST SEPARATION AND RECOVERY | ARCHER DANIELS MIDLAND COMPANY (US) | 2017-07-27 | — | — | WO | claimed |
| CN-104478794-B | Synthesis method of 2,6-dichloropyridine | 盐城恒盛化工有限公司 | 2017-04-12 | — | — | CN | claimed |
| CN-104478794-A | Synthesis method of 2,6-dichloropyridine | YANCHENG HENGSHENG CHEMICAL IND CO LTD | 2015-04-01 | — | — | CN | claimed |
| EP-0859768-B1 | AMINE ACID SALT COMPOUNDS AND PROCESS FOR THE PRODUCTION THEREOF | YOO SEO HONG (US) | 2003-01-08 | — | — | EP | claimed |
| EP-0859768-A4 | AMINE ACID SALT COMPOUNDS AND PROCESS FOR THE PRODUCTION THEREOF | YOO SEO HONG (US) | 1998-11-11 | — | — | EP | claimed |
| EP-0859768-A1 | AMINE ACID SALT COMPOUNDS AND PROCESS FOR THE PRODUCTION THEREOF | Yoo, Seo Hong (US) | 1998-08-26 | — | — | EP | claimed |
| US-5686588-A | Amine acid salt compounds and process for the production thereof | YOO SEO HONG (US) | 1997-11-11 | — | — | US | claimed |
| WO-1997007112-A1 | AMINE ACID SALT COMPOUNDS AND PROCESS FOR THE PRODUCTION THEREOF | YOO SEO HONG (US) | 1997-02-27 | — | — | WO | claimed |
| JP-1100158-A | — | — | None | — | — | JP | disclosed |
| US-12358877-B2 | Synthesis of 4-amino-5-methyl-1H-pyridin-2(1H)-on (intermediate compound for the synthesis of the MR antagonist finerenone) from 2-chloro-5-methyl-4-nitro-pyridine-1-oxide using the intermediate compound 2-chloro-5-methyl-4-pyridinamine | BAYER AKTIENGESELLSCHAFT (DE) | 2025-07-15 | — | — | US | disclosed |
| EP-3935045-B1 | SYNTHESIS OF 4-AMINO-5-METHYL-1H-PYRIDIN-2(1H)-ONE (INTERMEDIATE IN THE SYNTHESIS OF THE MR ANTAGONIST FINERENONE) FROM 2-CHLORO-5-METHYL-4-PYRIDINAMINE VIA THE INTERMEDIATE 2-CHLORO-5-METHYL-4-PYRIDINEAMINE | BAYER AG (DE) | 2025-05-21 | — | — | EP | disclosed |
| CN-119638617-A | Preparation method of 2, 3-dichloropyridine | 重庆华歌生物化学有限公司 | 2025-03-18 | — | — | CN | disclosed |
| CN-113474332-B | Method for synthesizing 4-amino-5-methyl-1H-pyridin-2-one | 拜耳公司 | 2025-03-04 | — | — | CN | disclosed |
| EP-0239904-A2 | Method of preparing 2,3,6-trichloropyridine and 2,3,5,6-tetrachloropyridine in the gas phase | MAKHTESHIM CHEMICAL WORKS LIMITED (IL) | 1987-10-07 | — | — | EP | disclosed |
| EP-0140927-A1 | PRODUCTION OF POLYCHLORINATED PYRIDINE MIXTURES BY LIQUID PHASE CHLORINATION OF 3,5-LUTIDINE OR 3,5-LUTIDINE HYDROCHLORIDE | KALAMA CHEMICAL, INC. (US) | 1985-05-15 | — | — | EP | disclosed |
| US-4515953-A | NONCATALYTIC | KALAMA CHEMICAL, INC. (US) | 1985-05-07 | — | — | US | disclosed |
| US-4507486-A | Production of polychlorinated pyridine mixtures by liquid phase chlorination of 3,5-lutidine or 3,5-lutidine hydrochloride | KALAMA CHEMICAL, INC. (US) | 1985-03-26 | — | — | US | disclosed |
| WO-1984004093-A1 | PRODUCTION OF POLYCHLORINATED PYRIDINE MIXTURES BY LIQUID PHASE CHLORINATION OF 3,5-LUTIDINE OR 3,5-LUTIDINE HYDROCHLORIDE | KALAMA CHEMICAL INC (US) | 1984-10-25 | — | — | WO | disclosed |