Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7264175

CCCCCCCCCCCCCNCc1ccccc1.Cl

nearest known ligand 0.77

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 15)

geneUniProtsupporting neighboursconfidence
▸ MAOA known ✓ P21397 1/20 0.77
▸ CHRM2 known ✓ P08172 1/20 0.74
▸ SIGMAR1 known ✓ Q99720 4/20 0.67
▸ HRH3 known ✓ Q9Y5N1 1/20 0.67
▸ GAA known ✓ P10253 1/20 0.57
▸ LMNA P02545 1/20 0.69
▸ HRH4 Q9H3N8 1/20 0.67
▸ CYP1A2 P05177 3/20 0.66
▸ CYP2D6 P10635 3/20 0.66
▸ CYP2C19 P33261 3/20 0.66
▸ SMN1; SMN2 Q16637 1/20 0.62
▸ MEN1 O00255 1/20 0.59
▸ KMT2A Q03164 1/20 0.59
▸ TDP1 Q9NUW8 1/20 0.59
▸ MAPT P10636 1/20 0.57

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 SCHEMBL28037282 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL6113017 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL5142852 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL4618378 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL1072926 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL15821301 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL11907511 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL1109937 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL21253049 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4
Hydrochloric Acid SCHEMBL15822816 1.00 MAOA (0.77) MAOACHRM2LMNASIGMAR1HRH4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 — — US claimed
US-4574158-A Acetal purification using phase transfer catalysts CONOCO INC. (US) 1986-03-04 — — US claimed
US-4513144-A Acetal purification with superoxides CONOCO INC. (US) 1985-04-23 — — US claimed
US-4412065-A Poly(oxy(silylene) esters) CONOCO INC. (US) 1983-10-25 — — US claimed
US-4379766-A Silyl esters of carboxylic acids by phase transfer catalysts CONOCO INC. (US) 1983-04-12 — — US claimed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 — — US claimed
EP-4342957-B1 OIL-RESISTANT AGENT DAIKIN IND LTD (JP) 2025-09-03 — — EP disclosed
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 — — US disclosed
EP-4342957-A1 OIL-RESISTANT AGENT DAIKIN INDUSTRIES, LTD. (JP) 2024-03-27 — — EP disclosed
US-20220097022-A1 A PROCESS FOR PREPARATION OF SUPERABSORBENT POLYMER UPL LTD (IN) 2022-03-31 — — US disclosed
EP-3917996-A1 A PROCESS FOR PREPARATION OF SUPERABSORBENT POLYMER UPL Ltd (IN) 2021-12-08 — — EP disclosed
CN-113316606-A Method for preparing superabsorbent polymer UPL有限公司 2021-08-27 — — CN disclosed
WO-2020157643-A1 A PROCESS FOR PREPARATION OF SUPERABSORBENT POLYMER UPL LTD (IN) 2020-08-06 — — WO disclosed
EP-0025846-A1 Improved process for the preparation of vinylcyclopropane derivatives NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1981-04-01 — — EP disclosed
US-4252739-A ALKYLATING AGENT SUCH AS 1,4-DIHALO-2-BUTENE, AN ACTIVE METHYLENE COMPOUND, A CATALYTIC ONIUM COMPOUND, AN ALKALI METAL COMPOUND AND WATER; ONE STEP EMERY INDUSTRIES, INC. (US) 1981-02-24 — — US disclosed
EP-0003835-A1 A hydroxy-urea, process for producing the same and a process for producing a phenyl-substituted N-methoxy-N-methyl-urea SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1979-09-05 — — EP disclosed
EP-0001825-A1 Method of preparing 2,4-difluoroaniline MERCK & CO. INC. (US) 1979-05-16 — — EP disclosed
US-4140719-A Solid-liquid phase transfer catalysis improved method of preparing 2,4-difluoroaniline MERCK & CO., INC. (US) 1979-02-20 — — US disclosed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 — — US disclosed
US-3969334-A SODIUM SILICATE TOYO SODA MANUFACTURING CO., LTD. (JA) 1976-07-13 — — US disclosed
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