Hydrochloric Acid

Hydrochloric Acid

SCHEMBL362843

C=Cc1ccc(C(=O)O)cc1.Cl

nearest known ligand 0.60

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
GLA known ✓ P06280 1/20 0.50
CA2 known ✓ P00918 2/20 0.48
DRD1 known ✓ P21728 1/20 0.48
ALDH1A1 P00352 5/20 0.60
TSHR P16473 4/20 0.57
TP53 P04637 1/20 0.57
KMT2A Q03164 1/20 0.54
TDP1 Q9NUW8 2/20 0.50
SRD5A2 P31213 2/20 0.50
POLB P06746 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
CA1 P00915 2/20 0.48
CA12 O43570 1/20 0.48
CA3 P07451 1/20 0.48
TYR P14679 1/20 0.48
CA4 P22748 1/20 0.48
CA6 P23280 1/20 0.48
CA5A P35218 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48

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
SCHEMBL16536 0.98 ALDH1A1 (0.62) ALDH1A1TSHRTP53KMT2ATDP1
SCHEMBL9742687 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
Bromide SCHEMBL3627952 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
Iodide SCHEMBL3628545 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
SCHEMBL8490138 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
SCHEMBL1059528 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
SCHEMBL11050679 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
SCHEMBL4344885 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
SCHEMBL1886825 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1
Ethylene SCHEMBL29074528 0.95 ALDH1A1 (0.60) ALDH1A1TSHRTP53KMT2ATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8507659-B2 Method for chemically modifying biopolymer and polypeptide FUJIFILM CORPORATION (JP) 2013-08-13 US claimed
US-7384990-B2 Latex particulates with active ester functional groups HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. (US) 2008-06-10 US claimed
US-20050282927-A1 Latex particulates with active ester functional groups HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2005-12-22 US claimed
US-12403447-B2 Separating agent for optical isomers DAICEL CORPORATION (JP) 2025-09-02 US disclosed
WO-2024176701-A1 RESIST COMPOSITION, RESIST PATTERN FORMATION METHOD, COMPOUND, AND POLYMER COMPOUND 東京応化工業株式会社 2024-08-29 WO disclosed
WO-2024176825-A1 METHOD FOR PRODUCING RADICAL POLYMERIZABLE GROUP-CONTAINING ORGANOPOLYSILOXANE, AND RADICAL POLYMERIZABLE GROUP-CONTAINING ORGANOPOLYSILOXANE 信越化学工業株式会社 2024-08-29 WO disclosed
WO-2024135498-A1 RESIST COMPOSITION, RESIST PATTERN FORMATION METHOD, AND COMPOUND 東京応化工業株式会社 2024-06-27 WO disclosed
CN-114502609-B Liquid crystal aligning agent, liquid crystal alignment film, liquid crystal element, polymer and compound JSR株式会社 2023-08-15 CN disclosed
WO-2023054507-A1 METHOD FOR PRODUCING STATIONARY PHASE FOR COLUMN CHROMATOGRAPHY 株式会社ダイセル 2023-04-06 WO disclosed
CN-114502609-A Liquid crystal aligning agent, liquid crystal alignment film, and liquid crystal element JSR株式会社 2022-05-13 CN disclosed
US-20210370270-A1 SEPARATING AGENT FOR OPTICAL ISOMERS DAICEL CORPORATION (JP) 2021-12-02 US disclosed
US-20070112103-A1 Molecular system and method for reversibly switching the same HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2007-05-17 US disclosed
US-7067587-B2 Polyolefin macromonomer, graft polymer obtained from the polyolefin macromonomer, and use thereof MITSUI CHEMICALS, INC. (JP) 2006-06-27 US disclosed
US-20040242791-A1 Polyolefin macromonomer, graft polymer obtained from the polyolefin macromonomer, and use thereof MITSUI CHEMICALS, INC. (JP) 2004-12-02 US disclosed
US-20040220346-A1 Multi-branched polymer, process for producing the same, and applications thereof MITSUI CHEMICALS, INC. (JP) 2004-11-04 US disclosed
EP-1457512-A1 Multi-branched polymer, process for producing the same, and applications thereof Mitsui Chemicals, Inc. (JP) 2004-09-15 EP disclosed
EP-1396504-A2 Polyolefin macromonomer, graft polymer obtained from the polyolefin macromonomer, and use thereof Mitsui Chemicals, Inc. (JP) 2004-03-10 EP disclosed
US-5626910-A CONTACTING RESIN WITH FLUORINE GAS FOR SURFACE MODIFIED MOLDED PRODUCT MITSUBISHI CHEMICAL CORPORATION (JP) 1997-05-06 US disclosed
US-5376499-A Highly heat-resistant positive resists comprising end-capped hydroxypolyamides SIEMENS AKTIENGESELLSCHAFT (DE) 1994-12-27 US disclosed
EP-0585662-A1 Surface-modified molded product of synthetic resin and process for producing it Mitsubishi Chemical Corporation (JP) 1994-03-09 EP disclosed