Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4305676

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

nearest known ligand 0.47

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
CHRM2 known ✓ P08172 2/20 0.32
CHRM4 known ✓ P08173 2/20 0.32
CHRM1 known ✓ P11229 2/20 0.32
HTR1A known ✓ P08908 1/20 0.30
CHRM5 known ✓ P08912 1/20 0.30
CHRM3 known ✓ P20309 1/20 0.30
CHRNB4 known ✓ P30926 1/20 0.30
CHRNA3 known ✓ P32297 1/20 0.30
CHRNA7 known ✓ P36544 1/20 0.30
PRKCA known ✓ P17252 2/20 0.30
TDP1 Q9NUW8 1/20 0.47
TSHR P16473 3/20 0.36
ALDH1A1 P00352 3/20 0.36
LMNA P02545 2/20 0.36
HSD17B10 Q99714 1/20 0.36
TBXA2R P21731 2/20 0.32
SMN1; SMN2 Q16637 3/20 0.31
MAPT P10636 2/20 0.31
GALR3 O60755 1/20 0.31
BLM P54132 1/20 0.31

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
SCHEMBL1020469 0.98 TDP1 (0.48) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL29104740 0.80 TDP1 (0.52) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL440977 0.78 TDP1 (0.50) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL31469524 0.78 TDP1 (0.50) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL13967844 0.77 TDP1 (0.48) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL425735 0.77 TDP1 (0.48) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL6225790 0.77 TDP1 (0.48) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL712304 0.77 TDP1 (0.48) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL7276080 0.77 TDP1 (0.48) TDP1TSHRALDH1A1LMNAHSD17B10
SCHEMBL6760890 0.76 TSHR (0.40) TDP1TSHRALDH1A1LMNAHSD17B10

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
WO-2009134030-A1 NOVEL PROCESS FOR PREPARATION OF IOPROMIDE LG LIFE SCIENCES LTD. (KR) 2009-11-05 WO 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