Hydrochloric Acid

Hydrochloric Acid

SCHEMBL150092

Cc1cccccccs1.Cl

nearest known ligand 0.38

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
ACHE known ✓ P22303 2/20 0.38
OPRM1 known ✓ P35372 1/20 0.31
TSHR P16473 3/20 0.38
LMNA P02545 1/20 0.38
ALOX12 P18054 1/20 0.38
HTT P42858 1/20 0.33
HPGDS O60760 1/20 0.32
DAO P14920 1/20 0.32
CYP3A4 P08684 2/20 0.31
TDP1 Q9NUW8 1/20 0.31
FBP1 P09467 1/20 0.31
CYP1A2 P05177 2/20 0.31
CYP2C19 P33261 2/20 0.31
CYP2D6 P10635 1/20 0.31
CYP2C9 P11712 1/20 0.31
RECQL P46063 1/20 0.31
OPRL1 P41146 1/20 0.31
KDM4E B2RXH2 1/20 0.30
HSD17B10 Q99714 1/20 0.30
PDPK1 O15530 1/20 0.30

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 SCHEMBL30018178 1.00 TSHR (0.38) TSHRACHELMNAALOX12HTT
Hydrochloric Acid SCHEMBL30492120 0.97 TSHR (0.36) TSHRACHELMNAALOX12HTT
Hydrochloric Acid SCHEMBL28785708 0.97 TSHR (0.36) TSHRACHELMNAALOX12HTT
SCHEMBL357322 0.97 TSHR (0.40) TSHRACHELMNAALOX12HTT
SCHEMBL30418396 0.97 TSHR (0.40) TSHRACHELMNAALOX12HTT
SCHEMBL29035078 0.94 TSHR (0.38) TSHRACHELMNAALOX12HPGDS
Water SCHEMBL17220159 0.94 TSHR (0.38) TSHRACHELMNAALOX12HPGDS
Iodide SCHEMBL27818959 0.94 TSHR (0.38) TSHRACHELMNAALOX12HPGDS
Water SCHEMBL1461353 0.94 TSHR (0.38) TSHRACHELMNAALOX12HPGDS
Hydrochloric Acid SCHEMBL27789351 0.92 TSHR (0.36) TSHRACHELMNAALOX12HPGDS

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3698140-A1 METHODS FOR MONITORING BLADDER CANCER IMMUNOTHERAPY NantBio, Inc. (US) 2020-08-26 EP claimed
US-20190117153-A1 METHODS FOR MONITORING BLADDER CANCER IMMUNOTHERAPY NANTBIO, INC. 2019-04-25 US claimed
WO-2019079009-A1 METHODS FOR MONITORING BLADDER CANCER IMMUNOTHERAPY NANTBIO, INC. (US) 2019-04-25 WO claimed
CN-108273516-A A kind of method that electrolytic manganese residues prepare effective catalyst and catalyzing hydrogen peroxide oxidative degradation methylene blue 北京森泉伟业科技有限公司 2018-07-13 CN claimed
EP-2046767-B1 PROCESS FOR PREPARING DIAMINOPHENOTHIAZINIUM COMPOUNDS PROVENCE TECHNOLOGIES (FR) 2015-04-22 EP claimed
US-8765942-B2 Process for preparing diaminophenothiazinium compounds PROVENCE TECHNOLOGIES (FR) 2014-07-01 US claimed
WO-2014096933-A1 SYSTEM FOR INHIBITING GLASS BOTTLE RE-USE BARTNING DIAZ CARLOS (MX) 2014-06-26 WO claimed
US-20140123718-A1 LIQUID PHOSPHATE FERTILIZER SOLUTION FOR AGRONOMIC USE ANTELO JOSÉ RAMÓN FLORENCIO (AR) 2014-05-08 US claimed
WO-2012012656-A2 MATERIALS AND METHODS FOR TREATING NEURODEGENERATIVE DISEASES UNIVERSITY OF SOUTH FLORIDA (US) 2012-01-26 WO claimed
US-20090291943-A1 PROCESS FOR PREPARING DIAMINOPHENOTHIAZINIUM COMPOUNDS PROVEPHARM LIFE SOLUTIONS (FR) 2009-11-26 US claimed
US-4361561-A METHYLENE BLUE Naylor, Graham John (GB) 1982-11-30 US claimed
CN-122055173-A Freeze-resistant injectable shear-thinning compositions 波士顿科学国际有限公司 2026-05-15 CN disclosed
US-12576140-B2 Cyclophilin 40 for reduction of neurotoxic fibrils and treatment of neurodegenerative diseases UNIVERSITY OF SOUTH FLORIDA (US) 2026-03-17 US disclosed
EP-4017496-B1 FORMULATIONS FOR USE IN THE PREVENTION AND/OR TREATMENT OF PERIPHERAL NEUROPATHY AND ITS ASSOCIATED DISEASES LOH YIN SZE (SG) 2026-01-07 EP disclosed
US-20250367466-A1 LIGHT THERAPY BED WITH ILLUMINATED MESH SUPPORT STRUCTURE POWER MEDICINE LLC (US) 2025-12-04 US disclosed
US-4548927-A Method and agents for raising animal tolerance to oxidant stress-inducing antibiotics EATON JOHN W (US) 1985-10-22 US disclosed
EP-0144402-A1 METHOD AND AGENTS FOR RAISING ANIMAL TOLERANCE TO OXIDANT STRESS-INDUCING ANTIBIOTICS EATON, John W. (US) 1985-06-19 EP disclosed
WO-1984004679-A1 METHOD AND AGENTS FOR RAISING ANIMAL TOLERANCE TO OXIDANT STRESS-INDUCING ANTIBIOTICS EATON JOHN W 1984-12-06 WO disclosed
US-4414212-A Method of treatment of pre-menstrual syndrome Naylor, Graham J. (GB) 1983-11-08 US disclosed
US-4361561-A METHYLENE BLUE Naylor, Graham John (GB) 1982-11-30 US 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 (2 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-12576140-B2 Cyclophilin 40 for reduction of neurotoxic fibrils and treatment of neurodegenerative diseases PSEN1, PSEN2, PRNP ACHE 1516/4885OPRM1 3691/4885TSHR 2889/4885
US-20090291943-A1 PROCESS FOR PREPARING DIAMINOPHENOTHIAZINIUM COMPOUNDS DCPS, QDPR, DNPEP ACHE 2384/4885OPRM1 990/4885TSHR 3603/4885

“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.