Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9492830

C=C(C)C(=O)OCC[N+](C)(C)C.Cl

nearest known ligand 0.63

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
▸ CHRM5 known ✓ P08912 6/20 0.63
▸ CHRM1 known ✓ P11229 6/20 0.63
▸ CHRM3 known ✓ P20309 6/20 0.63
▸ CHRM2 known ✓ P08172 5/20 0.59
▸ CHRM4 known ✓ P08173 5/20 0.59
▸ CHRNA7 known ✓ P36544 3/20 0.59
▸ HTR1A known ✓ P08908 2/20 0.59
▸ CHRNB4 known ✓ P30926 1/20 0.59
▸ CHRNA3 known ✓ P32297 1/20 0.59
▸ GAA known ✓ P10253 1/20 0.57
▸ ADRA2A known ✓ P08913 1/20 0.54
▸ ADRA1A known ✓ P35348 1/20 0.54
▸ ACHE known ✓ P22303 2/20 0.43
▸ CHRNB2 P17787 4/20 0.59
▸ CHRNA4 P43681 4/20 0.59
▸ SMN1; SMN2 Q16637 2/20 0.59
▸ PGR P06401 1/20 0.59
▸ TBXA2R P21731 1/20 0.59
▸ CHRNA10 Q9GZZ6 1/20 0.59
▸ CHRNA9 Q9UGM1 1/20 0.59

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 SCHEMBL28351837 1.00 CHRM5 (0.63) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL27653182 0.98 CHRM5 (0.61) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL22128479 0.98 CHRM5 (0.61) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL28918239 0.98 CHRM5 (0.61) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL28832470 0.98 CHRM5 (0.61) CHRM5CHRM1CHRM3CHRM2CHRM4
SCHEMBL180003 0.98 CHRM5 (0.65) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL30183040 0.98 CHRM5 (0.65) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL15954 0.98 CHRM5 (0.65) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL22128467 0.96 CHRM5 (0.59) CHRM5CHRM1CHRM3CHRM2CHRM4
Iodide SCHEMBL723953 0.96 CHRM5 (0.63) CHRM5CHRM1CHRM3CHRM2CHRM4

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5252629-A Adhesives for dentin GC CORPORATION (JP) 1993-10-12 — — US claimed
WO-2021112219-A1 SLUDGE DEHYDRATING AGENT AND SLUDGE DEHYDRATION METHOD 栗田工業株式会社 2021-06-10 — — WO disclosed
US-20170273881-A1 COSMETIC COMPOSITION FOR KERATIN FIBRES ALFA PARF GROUP S.P.A. (IT) 2017-09-28 — — US disclosed
US-20160250118-A1 METHOD AND COMPOSITION TO REMODELLING KERATINIC FIBER ALFA PARF GROUP S.P.A. (IT) 2016-09-01 — — US disclosed
US-20160194209-A1 BETA MOLECULAR SIEVE HAVING MULTI-LEVEL CHANNEL STRUCTURE AND PREPARATION METHOD THEREOF DALIAN INSTITUTE OF CHEMICAL PHYSICS, CHINESE ACADEMY OF SCIENCES (CN) 2016-07-07 — — US disclosed
EP-3037385-A1 BETA MOLECULAR SIEVE HAVING MULTI-LEVEL CHANNEL STRUCTURE, AND PREPARATION METHOD THEREOF Dalian Institute Of Chemical Physics, Chinese Academy of Sciences (CN) 2016-06-29 — — EP disclosed
CN-105372963-A charging roll, process cartridge, and image forming apparatus CANON KK 2016-03-02 — — CN disclosed
WO-2016026710-A1 COSMETIC COMPOSITION FOR KERATIN FIBRES ALFA PARF GROUP S.P.A. (IT) 2016-02-25 — — WO disclosed
US-5270055-A Solid pharmaceutical sustained-release form NORDMARK ARZNEIMITTEL GMBH (DE) 1993-12-14 — — 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-20160250118-A1 METHOD AND COMPOSITION TO REMODELLING KERATINIC FIBER KRT18, FABP2, CPT1A CHRM5 687/4885CHRM1 725/4885CHRM3 383/4885
US-20170273881-A1 COSMETIC COMPOSITION FOR KERATIN FIBRES KRT18, GRHPR, CUTA CHRM5 3088/4885CHRM1 4167/4885CHRM3 3267/4885

“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.

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