Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2070160

COC(=O)N[C@H]1CC[C@@H](OC)CC1.Cl

nearest known ligand 0.50

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 16)

geneUniProtsupporting neighboursconfidence
MMP8 known ✓ P22894 1/20 0.34
EPHX2 P34913 2/20 0.50
EPHX1 P07099 2/20 0.42
CD38 P28907 6/20 0.38
CYP2D6 P10635 1/20 0.36
CYP2B6 P20813 1/20 0.36
CYP2C19 P33261 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
CCNA2 P20248 3/20 0.36
CDK2 P24941 3/20 0.36
GSK3A P49840 2/20 0.36
GSK3B P49841 2/20 0.36
TSHR P16473 1/20 0.36
MAPT P10636 1/20 0.35
BRD4 O60885 1/20 0.34
MMP2 P08253 1/20 0.34

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
Hydrochloric Acid SCHEMBL28190843 1.00 EPHX2 (0.50) EPHX2EPHX1CD38CYP2D6CYP2B6
Hydrochloric Acid SCHEMBL3546089 1.00 EPHX2 (0.50) EPHX2EPHX1CD38CYP2D6CYP2B6
SCHEMBL2050427 0.87
SCHEMBL8464579 0.87 EPHX1 (0.46) EPHX2EPHX1NPSR1TSHRMAPT
SCHEMBL23684164 0.81 BTK (0.51) EPHX2EPHX1
SCHEMBL14175254 0.81 BTK (0.51) EPHX2EPHX1
SCHEMBL7936513 0.81 BTK (0.51) EPHX2EPHX1
SCHEMBL12409405 0.81 EPHX2 (0.51) EPHX2EPHX1CD38CYP2D6CYP2B6
SCHEMBL12409147 0.81 EPHX2 (0.51) EPHX2EPHX1CD38CYP2D6CYP2B6
SCHEMBL3539009 0.81 EPHX2 (0.51) EPHX2EPHX1CD38CYP2D6CYP2B6

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
US-7897803-B2 Cis-alkoxy-substituted spirocyclic 1H-pyrrolidine-2,4-dione derivatives serving as pesticides BAYER CROPSCIENCE AG (DE) 2011-03-01 US disclosed
US-7803967-B2 4-alkoxy-cyclohexane-1-amino-carboxylic esters and processes for their preparation BAYER CROPSCIENCE AG (DE) 2010-09-28 US disclosed
US-20100056598-A1 CIS-ALKOXY-SUBSTITUTED SPIROCYCLIC 1H-PYRROLIDINE-2,4-DIONE DERIVATIVES SERVING AS PESTICIDES BAYER INTELLECTUAL PROPERTY GMBH (DE) 2010-03-04 US disclosed
US-7638547-B2 Cis-alkoxy-substituted spirocyclic 1H-pyrrolidine-2,4-dione derivatives serving as pesticides BAYER CROPSCIENCE AG (DE) 2009-12-29 US disclosed
US-20090156402-A1 4-ALKOXY-CYCLOHEXANE-1-AMINO-CARBOXYLIC ESTERS AND PROCESSES FOR THEIR PREPARATION BAYER CROPSCIENCE AG (DE) 2009-06-18 US disclosed
US-7511153-B2 4-alkoxy cyclohexane-1 amino carboxylic acid esters and method for the production thereof BAYER CROPSCIENCE AG (DE) 2009-03-31 US disclosed
US-20070043219-A1 4-Alkoxy cyclohexane-1 amino carboxylic acid esters and method for the production thereof BAYER INTELLECTUAL PROPERTY GMBH (DE) 2007-02-22 US disclosed
US-20070032539-A1 Cis-alkoxy-substituted spirocyclic 1-h-pyrrolidine-2,4-dione derivatives serving as pesticides BAYER CROPSCIENCE AKTIENGESELLSCHAFT (DE) 2007-02-08 US disclosed
US-7148377-B2 4-Alkoxy cyclohexane-1-amino-carboxylic acid esters and method for the production thereof BAYER CROPSCIENCE AG (DE) 2006-12-12 US disclosed
US-20040039223-A1 4-Alkoxy cyclohexane-1 amino carboxylic acid esters and method for the production thereof BAYER INTELLECTUAL PROPERTY GMBH (DE) 2004-02-26 US 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 (5 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-20100056598-A1 CIS-ALKOXY-SUBSTITUTED SPIROCYCLIC 1H-PYRROLIDINE-2,4-DIONE DERIVATIVES SERVING AS PESTICIDES DDT, CYP4X1, CDY1; CDY1B MMP8 4616/4885EPHX2 149/4885EPHX1 266/4885
US-20070032539-A1 Cis-alkoxy-substituted spirocyclic 1-h-pyrrolidine-2,4-dione derivatives serving as pesticides DDT, CYP4X1, PDHX MMP8 4657/4885EPHX2 99/4885EPHX1 155/4885
US-20070043219-A1 4-Alkoxy cyclohexane-1 amino carboxylic acid esters and method for the production thereof ALDH7A1, DDC, ABAT MMP8 4492/4885EPHX2 268/4885EPHX1 388/4885
US-20090156402-A1 4-ALKOXY-CYCLOHEXANE-1-AMINO-CARBOXYLIC ESTERS AND PROCESSES FOR THEIR PREPARATION DDT, CYP4B1, ALDH7A1 MMP8 4421/4885EPHX2 177/4885EPHX1 255/4885
US-20040039223-A1 4-Alkoxy cyclohexane-1 amino carboxylic acid esters and method for the production thereof ALDH7A1, CYP51A1, ABAT MMP8 4594/4885EPHX2 354/4885EPHX1 495/4885

“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.