Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6897315

Cl.OCCNCc1ccccc1

nearest known ligand 0.72

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
GAA known ✓ P10253 1/20 0.65
MAOA known ✓ P21397 1/20 0.61
CHRM2 known ✓ P08172 1/20 0.59
SIGMAR1 known ✓ Q99720 3/20 0.55
DRD4 known ✓ P21917 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.72
MEN1 O00255 2/20 0.70
KMT2A Q03164 2/20 0.70
TDP1 Q9NUW8 1/20 0.70
MAPT P10636 1/20 0.65
LMNA P02545 1/20 0.54
MPO P05164 2/20 0.53
PDCD1 Q15116 1/20 0.53
CD274 Q9NZQ7 1/20 0.53
PKM P14618 1/20 0.52
THRB P10828 1/20 0.50
IDO1 P14902 1/20 0.50

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
SCHEMBL19401259 0.98 MEN1 (0.73) SMN1; SMN2MEN1KMT2ATDP1GAA
SCHEMBL177039 0.98 MEN1 (0.73) SMN1; SMN2MEN1KMT2ATDP1GAA
Bromide SCHEMBL11864024 0.95 MEN1 (0.70) SMN1; SMN2MEN1KMT2ATDP1GAA
Alcohol SCHEMBL11200660 0.94 SMN1; SMN2 (0.66) SMN1; SMN2MEN1KMT2ATDP1GAA
SCHEMBL6265883 0.93 SMN1; SMN2 (0.76) SMN1; SMN2MEN1KMT2ATDP1GAA
Hydrochloric Acid SCHEMBL8029205 0.90 CHRM2 (0.78) SMN1; SMN2MEN1KMT2ATDP1GAA
Diethanolamine SCHEMBL5343789 0.88 GAA (0.74) SMN1; SMN2MEN1KMT2ATDP1GAA
SCHEMBL7986639 0.88 CHRM2 (0.81) SMN1; SMN2MEN1KMT2ATDP1MAOA
N-Benzylmethylamine SCHEMBL781748 0.88 MAPT (0.63) SMN1; SMN2MEN1KMT2ATDP1GAA
Sulfuric Acid SCHEMBL28861186 0.88 MEN1 (0.59) SMN1; SMN2MEN1KMT2ATDP1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118185507-A Multilayer embossing precoating film and preparation method thereof 扬州市众和同盛包装材料有限公司 2024-06-14 CN claimed
CN-115926141-A Preparation method of cation-pi type coating modified carbon fiber and carbon fiber composite material 长春工业大学 2023-04-07 CN claimed
CN-118185507-A Multilayer embossing precoating film and preparation method thereof 扬州市众和同盛包装材料有限公司 2024-06-14 CN disclosed
CN-115058001-B Retarding monomer and preparation method thereof, retarding water reducer and preparation method thereof 科之杰新材料集团有限公司 2023-08-29 CN disclosed
CN-115926141-A Preparation method of cation-pi type coating modified carbon fiber and carbon fiber composite material 长春工业大学 2023-04-07 CN disclosed
CN-112226224-B Method for increasing crude oil recovery ratio 中国石油化工股份有限公司 2023-03-03 CN disclosed
CN-115667339-A Aqueous polyurethane resin dispersion 爱克发有限公司 2023-01-31 CN disclosed
CN-115058001-A Retarding monomer and preparation method thereof, retarding water reducer and preparation method thereof 科之杰新材料集团有限公司 2022-09-16 CN disclosed
CN-114929271-A Nanoemulsion compositions for the treatment of aeroallergen-related allergies and inflammation 密歇根大学董事会 2022-08-19 CN disclosed
CN-112708064-B Air-entraining and slow-setting type water reducing agent and preparation method thereof 科之杰新材料集团有限公司 2022-07-05 CN disclosed
CN-112708067-B Air-entraining monomer, air-entraining water reducer and preparation method thereof 科之杰新材料集团有限公司 2022-07-05 CN disclosed
CN-1948266-B Method of preparing N-mono substituted benzylamine by catalytic hydrogenation reduction amination UNIV TSINGHUA 2010-05-12 CN disclosed
CN-1948266-A Method of preparing N-mono substituted benzylamine by catalytic hydrogenation reduction amination UNIV TSINGHUA (CN) 2007-04-18 CN disclosed
US-6730784-B2 AS THERAPEUTIC AGENTS FOR AUTOIMMUNE DISEASES SUCH AS RHEUMATOID ARTHRITIS SANTEN PHARMACEUTICAL CO., LTD. (JP) 2004-05-04 US disclosed
US-20020198376-A1 Novel urea derivatives SANTEN PHARMACEUTICAL CO., LTD. (JP) 2002-12-26 US disclosed
US-6492370-B1 Urea derivatives and pharmaceutical compositions thereof SANTEN PHARMACEUTICAL CO., LTD. (JP) 2002-12-10 US disclosed
CN-1299344-A Novel urea derivatives SANTEN PHARCEUMATICAL CO LTD (JP) 2001-06-13 CN disclosed
EP-1072591-A1 NOVEL UREA DERIVATIVES SANTEN PHARMACEUTICAL CO., LTD. (JP) 2001-01-31 EP disclosed
US-4251660-A Method for preparing tetrahydroisoquinolines SMITHKLINE CORPORATION (US) 1981-02-17 US disclosed
US-4081030-A EPOXY RESIN, CURING AGENT, SOLVENT, COUPLING AGENT, QUATERNARY AMMONIUM HALIDE SURFACTANT, AND A PARTICULATE MATERIAL THE DOW CHEMICAL COMPANY (US) 1978-03-28 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 (1 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-20020198376-A1 Novel urea derivatives TNF, CTH, CFH GAA 2480/4885MAOA 731/4885CHRM2 315/4885

“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.