Hydrochloric Acid

Hydrochloric Acid

SCHEMBL231197

Cl.O=C(O)c1ccc(-c2ccccc2)cc1

nearest known ligand 0.95

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
EGFR known ✓ P00533 1/20 0.69
TSHR P16473 2/20 0.65
DAO P14920 1/20 0.65
NAPRT Q6XQN6 1/20 0.65
TP53 P04637 1/20 0.63
BCL2L1 Q07817 1/20 0.62
BAD Q92934 1/20 0.62
MAPT P10636 1/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
SRD5A2 P31213 2/20 0.61
CES2 O00748 1/20 0.61
CES1 P23141 1/20 0.61
NPC1 O15118 2/20 0.61
RAB9A P51151 2/20 0.61
MKNK1 Q9BUB5 1/20 0.61
MKNK2 Q9HBH9 1/20 0.61
CDC25B P30305 1/20 0.59
ATM Q13315 1/20 0.59
EPHX2 P34913 1/20 0.58
NR1H4 Q96RI1 1/20 0.58

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
Terephthalic Acid SCHEMBL10780545 0.97 EGFR (0.72) EGFRTSHRDAONAPRTTP53
SCHEMBL38562 0.97 EGFR (0.72) EGFRTSHRDAONAPRTTP53
Biphenyl SCHEMBL27749501 0.97 EGFR (0.72) EGFRTSHRDAONAPRTTP53
Biphenyl SCHEMBL5186249 0.97 EGFR (0.72) EGFRTSHRDAONAPRTTP53
SCHEMBL7155730 0.97 EGFR (0.72) EGFRTSHRDAONAPRTTP53
Benzene SCHEMBL28431643 0.97 EGFR (0.72) EGFRTSHRDAONAPRTTP53
SCHEMBL1584121 0.95 EGFR (0.69) EGFRTSHRDAONAPRTTP53
Biphenyl SCHEMBL9650627 0.95 EGFR (0.69) EGFRTSHRDAONAPRTTP53
Methane SCHEMBL20584283 0.95 EGFR (0.69) EGFRTSHRDAONAPRTTP53
SCHEMBL2596283 0.95 EGFR (0.69) EGFRTSHRDAONAPRTTP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240050419-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS CENTRE FOR DIGESTIVE DISEASES (AU) 2024-02-15 US claimed
US-20220184117-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS BORODY THOMAS JUJIS (AU) 2022-06-16 US claimed
EP-3955927-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS Borody, Thomas Julius (AU) 2022-02-23 EP claimed
EP-0899266-B1 Process for the production of benzoxazinones CIBA SC HOLDING AG (CH) 2003-01-15 EP claimed
US-6040443-A Process for the production of benzoxazinones CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-03-21 US claimed
EP-0899266-A1 Process for the production of benzoxazinones Ciba SC Holding AG (CH) 1999-03-03 EP claimed
JP-59174849-A None JP disclosed
US-20240050419-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS CENTRE FOR DIGESTIVE DISEASES (AU) 2024-02-15 US disclosed
CN-114644583-B Indole derivative and preparation method and application thereof 中国医学科学院医药生物技术研究所 2024-02-06 CN disclosed
US-11833140-B2 Compositions and methods for treating, ameliorating and preventing H. pylori infections CENTRE FOR DIGESTIVE DISEASES (AU) 2023-12-05 US disclosed
US-20220184117-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS BORODY THOMAS JUJIS (AU) 2022-06-16 US disclosed
EP-3955927-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS Borody, Thomas Julius (AU) 2022-02-23 EP disclosed
CN-111629728-A Compounds and methods for modulating adenosine A2B receptor and adenosine A2A receptor 科尔沃斯制药股份有限公司 2020-09-04 CN disclosed
US-4335054-A Process for the preparation of alkenylbenzenecarboxylic acid derivatives and alkenylnaphthalenecarboxylic acid derivatives CIBA-GEIGY CORPORATION (US) 1982-06-15 US disclosed
US-4335055-A Process for the preparation of alkenylbenzene derivatives or alkenylnaphthalene derivatives CIBA-GEIGY CORPORATION (US) 1982-06-15 US disclosed
US-4214099-A Intermediates for synthesis of precursors for prostaglandins PFIZER INC. (US) 1980-07-22 US disclosed
US-4122093-A Process for preparing a lactone PFIZER INC. (US) 1978-10-24 US disclosed
US-4029835-A MADE BY PRESSING AND HEATING A MIXED WEB OF TWO AROMATIC POLYAMIDES MITSUBISHI RAYON CO., LTD. (JA) 1977-06-14 US disclosed
US-3992438-A Novel prostaglandin intermediates PFIZER INC. (US) 1976-11-16 US disclosed
US-3943151-A Prostaglandin intermediates PFIZER INC. (US) 1976-03-09 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-20220184117-A1 COMPOSITIONS AND METHODS FOR TREATING, AMELIORATING AND PREVENTING H. PYLORI INFECTIONS ATP1A2, ATP4A, ATP1A3 EGFR 4754/4885TSHR 3723/4885DAO 1559/4885

“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.