Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4305679

CC(=O)OCC(CN)OC(C)=O.Cl

nearest known ligand 0.52

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 17)

geneUniProtsupporting neighboursconfidence
PRKCA known ✓ P17252 4/20 0.40
GAA known ✓ P10253 1/20 0.38
HRH1 known ✓ P35367 1/20 0.35
CHRM2 known ✓ P08172 1/20 0.32
CHRM4 known ✓ P08173 1/20 0.32
CHRM1 known ✓ P11229 1/20 0.32
TDP1 Q9NUW8 1/20 0.52
AR P10275 1/20 0.39
LMNA P02545 2/20 0.36
TSHR P16473 2/20 0.36
ALDH1A1 P00352 1/20 0.36
HSD17B10 Q99714 1/20 0.36
MEN1 O00255 1/20 0.35
CYP1A2 P05177 1/20 0.35
KMT2A Q03164 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
TBXA2R P21731 1/20 0.32

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
SCHEMBL1020470 0.98 TDP1 (0.53) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL28165091 0.87 TDP1 (0.54) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL9420964 0.85 TDP1 (0.52) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL3870 0.84 TDP1 (0.56) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL821340 0.84 TDP1 (0.56) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL16446056 0.82 TDP1 (0.54) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL4367394 0.82 TDP1 (0.54) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL31035933 0.82 TDP1 (0.54) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL16445622 0.82 TDP1 (0.54) TDP1PRKCAARGAALMNA
Triacetin SCHEMBL8012678 0.82 TDP1 (0.54) TDP1PRKCAARGAALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009134030-A1 NOVEL PROCESS FOR PREPARATION OF IOPROMIDE LG LIFE SCIENCES LTD. (KR) 2009-11-05 WO claimed
US-4675131-A Organic quaternary ammonium compounds and process for the preparation thereof INTEROX(SOCIETE ANONYME) (BE) 1987-06-23 US claimed
CN-102015624-B Preparation method of iopromide LG LIFE SCIENCES LTD 2013-11-06 CN disclosed
US-8420858-B2 Process for preparation of iopromide LG LIFE SCIENCES LTD. (KR) 2013-04-16 US disclosed
US-8420858-B2 Process for preparation of iopromide LG LIFE SCIENCES LTD. (KR) 2013-04-16 US disclosed
CN-102015624-A New preparation method of iopromide LG LIFE SCIENCES LTD 2011-04-13 CN disclosed
WO-2009134030-A1 NOVEL PROCESS FOR PREPARATION OF IOPROMIDE LG LIFE SCIENCES LTD. (KR) 2009-11-05 WO disclosed
WO-2009134030-A1 NOVEL PROCESS FOR PREPARATION OF IOPROMIDE LG LIFE SCIENCES LTD. (KR) 2009-11-05 WO disclosed
EP-0835259-A1 IODINE-CONTAINING PEPTIDES AND THEIR USE AS X-RAY CONTRAST MEDIA SCHERING AKTIENGESELLSCHAFT (DE) 1998-04-15 EP disclosed
WO-1996040760-A2 IODINE-CONTAINING PEPTIDES AND THEIR USE AS X-RAY CONTRAST MEDIA SCHERING AKTIENGESELLSCHAFT (DE) 1996-12-19 WO disclosed
US-5073362-A DICARBOXYLIC ACID-BIS(3,5-DICARBAMOYL-2,4,6-TRIIODOANILIDES) AND X-RAY CONTRAST MEDIA CONTAINING THEM SCHERING AKTIENGESELLSCHAFT (DE) 1991-12-17 US disclosed