Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4398174

C=CCC(N)(Cc1ccccc1)C(=O)O.Cl

nearest known ligand 0.53

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 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.53
HIF1A Q16665 1/20 0.53
ARG1 P05089 2/20 0.50
ARG2 P78540 2/20 0.50
ALDH1A1 P00352 2/20 0.49
TSHR P16473 1/20 0.49
HTT P42858 1/20 0.46
CYP2C19 P33261 4/20 0.43
CYP2C9 P11712 3/20 0.43
CYP3A4 P08684 3/20 0.43
TAAR1 Q96RJ0 1/20 0.40
MAPK1 P28482 1/20 0.37
BLM P54132 1/20 0.37
KMT2A Q03164 1/20 0.36
FDPS P14324 1/20 0.36
ATM Q13315 1/20 0.35
CYP1A2 P05177 2/20 0.35
RECQL P46063 1/20 0.35
CYP2D6 P10635 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
Hydrochloric Acid SCHEMBL4398176 1.00 SMN1; SMN2 (0.53) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL4396691 0.98 SMN1; SMN2 (0.55) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL4396692 0.98 SMN1; SMN2 (0.55) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL9551389 0.87 HTT (0.54) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL9551388 0.87 HTT (0.54) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL12583561 0.85 SMN1; SMN2 (0.47) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL8351006 0.82 SMN1; SMN2 (0.69) SMN1; SMN2HIF1AARG1ARG2TSHR
SCHEMBL27420773 0.81 ALDH1A1 (0.46) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL8903660 0.78 SMN1; SMN2 (0.51) SMN1; SMN2HIF1AARG1ARG2ALDH1A1
SCHEMBL28910344 0.78 PPARA (0.42) ARG1ARG2ALDH1A1TSHRCYP2C19

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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7511039-B2 β-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins MYRIAD GENETICS, INC. (US) 2009-03-31 US disclosed
US-20060293372-A1 Beta-sheet mimetics and methods relating to the use thereof MYRIAD GENETICS, INC. (US) 2006-12-28 US disclosed
US-20060276408-A1 Beta-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins MYRIAD GENETICS, INCORPORATED (US) 2006-12-07 US disclosed
US-7125872-B2 β-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins MYRIAD GENETICS, INC. (US) 2006-10-24 US disclosed
EP-1661566-A2 Use of beta-sheet mimetics as protease and kinase inhibitors and as inhibitors of transcription factors MYRIAD GENETICS, INC. (US) 2006-05-31 EP disclosed
EP-0915700-B1 USE OF BETA-SHEET MIMETICS AS PROTEASE AND KINASE INHIBITORS AND AS INHIBITORS OF TRANSCRIPTION FACTORS MYRIAD GENETICS INC (US) 2006-03-22 EP disclosed
US-20040230035-A1 Beta-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins MYRIAD GENETICS, INC. (US) 2004-11-18 US disclosed
US-6699869-B1 PROTEASE INHIBITORS, ANTICOAGULANT MYRIAD GENETICS INC. 2004-03-02 US disclosed
US-20030191109-A1 Beta-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins KAHN MICHAEL (US) 2003-10-09 US disclosed
US-6586426-B1 Pyrrolizine derivatives; thrombin, elastase, and factor X inhibitors MOLECUMETICS LTD. 2003-07-01 US disclosed
EP-1053246-A1 BETA-SHEET MIMETICS AND METHODS RELATING TO THE USE THEREOF MOLECUMETICS, LTD. (US) 2000-11-22 EP disclosed
US-6117896-A Methods for regulating transcription factors MOLECUMETICS LTD. (US) 2000-09-12 US disclosed
US-6020331-A β-sheet mimetics and use thereof as protease inhibitors MOLECUMETICS, LTD. (US) 2000-02-01 US disclosed
WO-1999041276-A1 β-SHEET MIMETICS AND METHODS RELATING TO THE USE THEREOF MOLECUMETICS LTD. (US) 1999-08-19 WO disclosed
EP-0915700-A1 USE OF BETA-SHEET MIMETICS AS PROTEASE AND KINASE INHIBITORS AND AS INHIBITORS OF TRANSCRIPTION FACTORS MOLECUMETICS, LTD. (US) 1999-05-19 EP disclosed
WO-1998005333-A1 USE OF BETA-SHEET MIMETICS AS PROTEASE AND KINASE INHIBITORS AND AS INHIBITORS OF TRANSCRIPTION FACTORS MOLECUMETICS LTD. (US) 1998-02-12 WO disclosed
EP-0817642-A1 $g(b)-SHEET MIMETICS AND USE THEREOF AS INHIBITORS OF BIOLOGICALLY ACTIVE PEPTIDES OR PROTEINS MOLECUMETICS, LTD. (US) 1998-01-14 EP disclosed
EP-0815123-A1 $g(b)-SHEET MIMETICS AND USE THEREOF AS PROTEASE INHIBITORS MOLECUMETICS, LTD. (US) 1998-01-07 EP disclosed
WO-1996030035-A1 β-SHEET MIMETICS AND USE THEREOF AS INHIBITORS OF BIOLOGICALLY ACTIVE PEPTIDES OR PROTEINS MOLECUMETICS LTD. (US) 1996-10-03 WO disclosed
WO-1996030396-A1 β-SHEET MIMETICS AND USE THEREOF AS PROTEASE INHIBITORS MOLECUMETICS LTD. (US) 1996-10-03 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 (3 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-20060293372-A1 Beta-sheet mimetics and methods relating to the use thereof SERBP1, PACSIN2, HGFAC SLC6A2 4538/4885SMN1; SMN2 2257/4885HIF1A 512/4885
US-20030191109-A1 Beta-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins MICA, BMX, CD74 SLC6A2 4079/4885SMN1; SMN2 2466/4885HIF1A 1268/4885
US-20060276408-A1 Beta-sheet mimetics and use thereof as inhibitors of biologically active peptides or proteins SERPINB1, SERPINE1, SERPINA2 SLC6A2 4801/4885SMN1; SMN2 1259/4885HIF1A 1965/4885

“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.