Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2528348

C=CCOC(=O)NCCN.Cl

nearest known ligand 0.41

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
CACNA1B known ✓ Q00975 1/20 0.41
HRH3 known ✓ Q9Y5N1 2/20 0.34
ACHE known ✓ P22303 1/20 0.33
MAPT P10636 2/20 0.41
APBA1 Q02410 1/20 0.41
MEN1 O00255 2/20 0.37
KMT2A Q03164 2/20 0.37
ERN1 O75460 4/20 0.36
CYP3A4 P08684 1/20 0.35
CASP1 P29466 5/20 0.35
TSHR P16473 2/20 0.34
ALDH1A1 P00352 2/20 0.34
HSD17B10 Q99714 1/20 0.34
HRH4 Q9H3N8 2/20 0.34
BLM P54132 1/20 0.33
PMP22 Q01453 1/20 0.33

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
SCHEMBL7001155 0.98 MAPT (0.42) MAPTCACNA1BAPBA1MEN1KMT2A
Hydrochloric Acid SCHEMBL28852389 0.89 DDAH1 (0.39) MAPTCACNA1BAPBA1MEN1KMT2A
Hydrochloric Acid SCHEMBL28713623 0.87 DDAH1 (0.45) MAPTCACNA1BAPBA1ERN1HRH4
SCHEMBL28255342 0.87 ACHE (0.40) MAPTCACNA1BAPBA1MEN1KMT2A
Trifluoroacetic Acid SCHEMBL1276411 0.87 CASP1 (0.36) MAPTCACNA1BAPBA1MEN1KMT2A
Hydrochloric Acid SCHEMBL2525927 0.86 PAOX (0.46) ERN1ACHE
SCHEMBL13055388 0.86 MAPT (0.42) MAPTCACNA1BAPBA1MEN1KMT2A
SCHEMBL1276392 0.85 DDAH1 (0.46) MAPTCACNA1BAPBA1MEN1KMT2A
SCHEMBL20207166 0.84 PAOX (0.47) MAPTCACNA1BAPBA1ERN1TSHR
SCHEMBL6951293 0.84 PAOX (0.47) MAPTCACNA1BAPBA1ERN1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4077485-B1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS DISPERSIONS WACKER CHEMIE AG (DE) 2023-05-17 EP claimed
US-20220372195-A1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS DISPERSIONS WACKER CHEMIE AG (DE) 2022-11-24 US claimed
EP-4077485-A1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS DISPERSIONS Wacker Chemie AG (DE) 2022-10-26 EP claimed
CN-114829456-A Crosslinkable reactive silicone organic copolymer dispersions 瓦克化学股份公司 2022-07-29 CN claimed
WO-2021126174-A1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS DISPERSIONS WACKER CHEMIE AG (DE) 2021-06-24 WO claimed
US-9850327-B2 Use of modified water-soluble polymers as crosslinking auxiliary agents WACKER CHEMIE AG (DE) 2017-12-26 US claimed
EP-3049450-B1 USE OF MODIFIED WATER-SOLUBLE POLYMERS AS CROSSLINKING AUXILIARY AGENTS WACKER CHEMIE AG (DE) 2017-11-08 EP claimed
US-20160208031-A1 USE OF MODIFIED WATER-SOLUBLE POLYMERS AS CROSSLINKING AUXILIARY AGENTS WACKER CHEMIE AG (DE) 2016-07-21 US claimed
US-8637613-B2 Self-dispersible silicone copolymers and method for the production and use thereof WACKER CHEMIE AG (DE) 2014-01-28 US claimed
US-20100041822-A1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS AND METHOD FOR THE PRODUCTION AND USE THEREOF WACKER CHEMIE AG (DE) 2010-02-18 US claimed
WO-2025133027-A1 PROCESS FOR FORMING A COATING COMPOSITION, A COATING COMPOSITION, AND AN ARTICLE COMPRISING THE SAME WACKER CHEMIE AG (DE) 2025-06-26 WO disclosed
CN-115245589-B Novel degradable embolism microsphere with controllable particle size and preparation method thereof 苏州浩微生物医疗科技有限公司 2024-08-20 CN disclosed
CN-115245591-B Degradable embolism microsphere and preparation method thereof 苏州浩微生物医疗科技有限公司 2024-06-14 CN disclosed
EP-4077485-B1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS DISPERSIONS WACKER CHEMIE AG (DE) 2023-05-17 EP disclosed
CN-114829456-B Crosslinkable reactive silicone organic copolymer dispersions 瓦克化学股份公司 2023-04-28 CN disclosed
US-20110257297-A1 Graft Copolymers and Use Thereof as Low-Profile Additives WACKER CHEMIE AG (DE) 2011-10-20 US disclosed
US-20100273934-A1 CROSSLINKABLE VINYL ESTER COPOLYMERS AND THEIR USE AS LOW-PROFILE ADDITIVES WACKER CHEMIE AG (DE) 2010-10-28 US disclosed
US-20100227995-A1 PRODUCTION OF VINYL ACETATE - VINYL ESTER COPOLYMERS HAVING A LOW CONTENT OF HIGH-BOILING VINYL ESTERS WACKER CHEMIE AG (DE) 2010-09-09 US disclosed
US-20100041822-A1 CROSSLINKABLE REACTIVE SILICONE ORGANIC COPOLYMERS AND METHOD FOR THE PRODUCTION AND USE THEREOF WACKER CHEMIE AG (DE) 2010-02-18 US disclosed
US-20100010165-A1 SELF-DISPERSIBLE SILICONE COPOLYMERS AND METHOD FOR THE PRODUCTION AND USE THEREOF WACKER CHEMIE AG (DE) 2010-01-14 US disclosed