Hydrochloric Acid

Hydrochloric Acid

SCHEMBL588959

CCCCNCc1ccccc1.Cl

nearest known ligand 0.69

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
MAOA known ✓ P21397 1/20 0.69
CHRM2 known ✓ P08172 1/20 0.67
SIGMAR1 known ✓ Q99720 4/20 0.62
GAA known ✓ P10253 1/20 0.61
HRH3 known ✓ Q9Y5N1 1/20 0.60
SCN8A known ✓ Q9UQD0 1/20 0.53
MEN1 O00255 1/20 0.64
KMT2A Q03164 1/20 0.64
TDP1 Q9NUW8 1/20 0.64
MAPT P10636 1/20 0.61
HRH4 Q9H3N8 1/20 0.60
CYP1A2 P05177 3/20 0.59
CYP2D6 P10635 3/20 0.59
CYP2C19 P33261 3/20 0.59
LMNA P02545 1/20 0.58
SMN1; SMN2 Q16637 1/20 0.56
MPO P05164 1/20 0.51

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
SCHEMBL41690 0.98 MAOA (0.72) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL28054971 0.96 MAOA (0.69) MAOACHRM2MEN1KMT2ATDP1
Iodide SCHEMBL3001589 0.96 MAOA (0.69) MAOACHRM2MEN1KMT2ATDP1
Ammonia Solution, Strong SCHEMBL28964330 0.96 MAOA (0.69) MAOACHRM2MEN1KMT2ATDP1
Bromide SCHEMBL2577914 0.96 MAOA (0.69) MAOACHRM2MEN1KMT2ATDP1
Water SCHEMBL28180553 0.96 MAOA (0.69) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL16439697 0.94 CHRM2 (0.70) MAOACHRM2MEN1KMT2ATDP1
Hydrochloric Acid SCHEMBL28284417 0.94 MAOA (0.73) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL29306651 0.94 CHRM2 (0.70) MAOACHRM2MEN1KMT2ATDP1
Hydrochloric Acid SCHEMBL1072926 0.92 MAOA (0.77) MAOACHRM2MEN1KMT2ATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2417110-B1 A ONE POT PROCESS FOR PREPARING 2-BUTYL-3-[[2'-(1H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-1,3-DIAZASPIRO [4, 4]NON-1-EN-4-ONE (IRBESARTAN) CTX LIFE SCIENCES PVT LTD (IN) 2014-05-07 EP claimed
US-8609859-B2 One pot process for preparing 2-butyl-3-[[2′-(1H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1,3-diazaspiro [4, 4] non-1-en-4-one (irbesartan) CTX LIFE SCIENCES PVT. LTD. (IN) 2013-12-17 US claimed
US-20120116093-A1 ONE POT PROCESS FOR PREPARING 2-BUTYL-3-[[2'-(1H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-1,3-DIAZASPIRO [4, 4] NON-1-EN-4-ONE (IRBESARTAN) CTX Life Sciences Pvt. Ltd (IN) 2012-05-10 US claimed
EP-2417110-A2 A ONE POT PROCESS FOR PREPARING 2-BUTYL-3-[[2'-(1H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-1,3-DIAZASPIRO [4, 4]NON-1-EN-4-ONE (IRBESARTAN) CTX Life Sciences Pvt. Ltd. (IN) 2012-02-15 EP claimed
WO-2011154860-A1 AN IMPROVED PROCESS FOR PREPARING ILOPERIDONE ALEMBIC PHARMACEUTICALS LIMITED (IN) 2011-12-15 WO claimed
WO-2010116380-A2 A ONE POT PROCESS FOR PREPARING 2-BUTYL-3-[[2'-(1H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-1,3-DIAZASPIRO [4, 4] NON-1-EN-4-ONE (IRBESARTAN) CTX LIFE SCIENCES PVT. LTD. (IN) 2010-10-14 WO claimed
US-20060252940-A1 CRYSTALLINE 1-[2-(2,4-DIFLUOROPHENYL)-OXIRANYL METHYL]-1H-1,2,4-TRIAZOLE DR. REDDY'S LABORATORIES, INC. 2006-11-09 US claimed
JP-3054468-A None JP disclosed
WO-2025099119-A1 A NOVEL AND HIGHLY COST-EFFICIENT TELESCOPING SYNTHESIS OF 2-METHOXYMETHYL-P-PHENYLENEDIAMINE WELLA GERMANY GMBH (DE) 2025-05-15 WO disclosed
EP-2934563-B1 ANTIMICROBIAL COMPOUNDS, THEIR SYNTHESIS AND APPLICATIONS THEREOF JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENT RESEARCH (IN) 2020-07-08 EP disclosed
CN-109153846-A Resin composition, electrophotographic photoreceptor, and electrophotographic apparatus 出光兴产株式会社 2019-01-04 CN disclosed
US-9783490-B2 Antimicrobial compounds, their synthesis and applications thereof THE SECRETARY OF STATE FOR HEALTH (GB) 2017-10-10 US disclosed
CN-106662820-A Silicon-containing resist underlayer film forming composition having halogenated sulfonylalkyl group 日产化学工业株式会社 2017-05-10 CN disclosed
CN-1275123-A Prostaglandin agonists and their use to treat bone disorders PFIZER (US) 2000-11-29 CN disclosed
JP-H0354468-A SEPARATION OF STEROID SULFATE IN BLOOD NISHIKAZE OSAMU 1991-03-08 JP disclosed
EP-0229098-A1 PLANT GROWTH REGULATING COMPOSITIONS AND PROCESS FOR REGULATING PLANT GROWTH MéM NÖVéNYVéDELMI éS AGROKéMIAI KÖZPONT (HU) 1987-07-22 EP disclosed
EP-0109039-B1 BENZO(F)QUINOLINE DERIVATIVES Yoshitomi Pharmaceutical Industries, Ltd. (JP) 1987-02-25 EP disclosed
WO-1986007237-A1 PLANT GROWTH REGULATING COMPOSITIONS AND PROCESS FOR REGULATING PLANT GROWTH MÉM NÖVÉNYVÉDELMI ÉS AGROKÉMIAI KÖZPONT (HU) 1986-12-18 WO disclosed
US-4543354-A Anti-hypertensive 9-aminomethyl-benzo[f]quinoline-3,10-dione derivatives YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1985-09-24 US disclosed
EP-0109039-A1 Benzo(f)quinoline derivatives Yoshitomi Pharmaceutical Industries, Ltd. (JP) 1984-05-23 EP 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-20060252940-A1 CRYSTALLINE 1-[2-(2,4-DIFLUOROPHENYL)-OXIRANYL METHYL]-1H-1,2,4-TRIAZOLE CYP2F1, CYP4B1, CYP3A4 MAOA 1125/4885CHRM2 2732/4885SIGMAR1 2204/4885
US-20120116093-A1 ONE POT PROCESS FOR PREPARING 2-BUTYL-3-[[2'-(1H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-1,3-DIAZASPIRO [4, 4] NON-1-EN-4-ONE (IRBESARTAN) PKD1, AGTR1, NPR1 MAOA 4113/4885CHRM2 1242/4885SIGMAR1 63/4885

“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.