Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4897724

Cl.O=C(Cl)CN1CCNCC1

nearest known ligand 0.61

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 Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CHRM5 known ✓ P08912 2/20 0.48
CHRM3 known ✓ P20309 2/20 0.48
SIGMAR1 known ✓ Q99720 7/20 0.44
CA2 known ✓ P00918 2/20 0.37
GAA known ✓ P10253 1/20 0.36
CA12 O43570 1/20 0.37
CA1 P00915 1/20 0.37
CA9 Q16790 1/20 0.37
CXCR4 P61073 2/20 0.36
KDM4E B2RXH2 1/20 0.36
HSD17B10 Q99714 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
CHKA P35790 1/20 0.35

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
SCHEMBL2991895 0.98 CHRM5 (0.50) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL1373260 0.79 CHRM5 (0.50) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL31505485 0.79 CHRM5 (0.50) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL4441607 0.79 CHRM5 (0.50) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL114328 0.78 GAA (0.50) KDM4EGAAL3MBTL1
SCHEMBL30733932 0.78 CHRM5 (0.53) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL4681 0.77 KDM4E (0.54) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL3925566 0.77 CHRM5 (0.53) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL28968883 0.77 CHRM5 (0.48) CHRM5CHRM3SIGMAR1CA2CA12
Hydrochloric Acid SCHEMBL1546636 0.77 KDM4E (0.54) CHRM5CHRM3SIGMAR1CA2CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102675319-A Method for preparing dexzopiclone SHANGHAI ZNBIOCHEM CO LTD 2012-09-19 CN claimed
CN-102675318-A Chiral synthesis of Eszopiclone SHANGHAI ZNBIOCHEM CO LTD 2012-09-19 CN claimed
CN-102675318-A Chiral synthesis of Eszopiclone SHANGHAI ZNBIOCHEM CO LTD 2012-09-19 CN disclosed
CN-102675319-A Method for preparing dexzopiclone SHANGHAI ZNBIOCHEM CO LTD 2012-09-19 CN disclosed
CN-102675319-A Method for preparing dexzopiclone SHANGHAI ZNBIOCHEM CO LTD 2012-09-19 CN disclosed
EP-1904499-A1 PROCESS FOR THE PREPARATION OF ZOPICLONE Teva Pharmaceutical Industries Ltd (IL) 2008-04-02 EP disclosed
US-20080015197-A1 Process for the preparatrion of zopiclone TEVA PHARMACEUTICALS USA, INC. 2008-01-17 US disclosed
WO-2008002629-A1 PROCESS FOR THE PREPARATION OF ZOPICLONE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2008-01-03 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 (1 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-20080015197-A1 Process for the preparatrion of zopiclone CYP3A5, CYP3A7, CYP3A43 CHRM5 940/4885CHRM3 868/4885SIGMAR1 769/4885

“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.