Hydrochloric Acid

Hydrochloric Acid

SCHEMBL21824331

Cl.O=C1COc2ccncc2N1

nearest known ligand 0.54

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 16)

geneUniProtsupporting neighboursconfidence
PARP1 known ✓ P09874 3/20 0.46
PDE3B known ✓ Q13370 1/20 0.40
PDE3A known ✓ Q14432 1/20 0.40
GAA known ✓ P10253 2/20 0.40
CYP11B1 P15538 2/20 0.54
CYP11B2 P19099 2/20 0.54
MMP12 P39900 1/20 0.50
NR3C2 P08235 3/20 0.44
ALDH1A1 P00352 5/20 0.44
KMT2A Q03164 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
MAPT P10636 4/20 0.42
HPGD P15428 1/20 0.42
PKM P14618 1/20 0.40
KDM4E B2RXH2 1/20 0.39

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
SCHEMBL1191106 0.98 CYP11B1 (0.55) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL1190878 0.84 CYP11B1 (0.58) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL7328231 0.81 CYP11B1 (0.40) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL5214057 0.74 ALDH1A1 (0.60) CYP11B1CYP11B2MMP12PARP1NR3C2
Hydrochloric Acid SCHEMBL30293243 0.74 MMP12 (0.56) CYP11B1CYP11B2MMP12PARP1NR3C2
Hydrochloric Acid SCHEMBL6518631 0.74 MMP12 (0.56) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL30494187 0.73 NR3C2 (0.55) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL26463277 0.73 NR3C2 (0.55) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL21004232 0.73 MMP12 (0.44) CYP11B1CYP11B2MMP12PARP1NR3C2
SCHEMBL10552765 0.72 CYP11B1 (0.40) CYP11B1CYP11B2MMP12NR3C2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260070923-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND JW PHARMACEUTICAL CORP (KR) 2026-03-12 US disclosed
US-12497410-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound JW PHARMACEUTICAL CORPORATION (KR) 2025-12-16 US disclosed
CN-119143779-A Process for preparing heterocyclic derivative compounds, compositions containing the compounds and hydrates of the compounds JW 制药公司 2024-12-17 CN disclosed
EP-3909956-B1 HYDROCHLORIDE SALT 1.5 HYDRATE OF AN HETEROCYCLIC DERIVATIVE COMPOUND JW PHARMACEUTICAL CORP (KR) 2024-12-04 EP disclosed
US-12103938-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound JW PHARMACEUTICAL CORPORATION (KR) 2024-10-01 US disclosed
CN-114085235-B Process for preparing heterocyclic derivative compounds, compositions containing the compounds and hydrates of the compounds JW 制药公司 2024-08-13 CN disclosed
US-12030895-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound JW PHARMACEUTICAL CORPORATION (KR) 2024-07-09 US disclosed
US-20240083911-A1 Method For Preparing Heterocyclic Derivative Compound, Composition Containing Same Compound, And Hydrate of Same Compound JW PHARMACEUTICAL CORPORATION (KR) 2024-03-14 US disclosed
US-20240067659-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND JW PHARMACEUTICAL CORPORATION (KR) 2024-02-29 US disclosed
US-11866448-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound JW PHARMACEUTICAL CORPORATION (KR) 2024-01-09 US disclosed
US-20220363691-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND JW PHARMACEUTICAL CORPORATION (KR) 2022-11-17 US disclosed
US-20220340594-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND JW PHARMACEUTICAL CORPORATION (KR) 2022-10-27 US disclosed
EP-3909955-A1 A PHARMACEUTICAL COMPOSITION COMPRISING A HETEROCYCLIC DERIVATIVE FOR USE IN THE TREATMENT OF HYPERURICEMIA JW Pharmaceutical Corporation (KR) 2021-11-17 EP disclosed
EP-3909956-A1 HYDROCHLORIDE SALT 1.5 HYDRATE OF AN HETEROCYCLIC DERIVATIVE COMPOUND JW Pharmaceutical Corporation (KR) 2021-11-17 EP disclosed
EP-3632917-B1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE JW PHARMACEUTICAL CORP (KR) 2021-11-17 EP disclosed
US-20200207784-A1 Method For Preparing Heterocyclic Derivative Compound, Composition Containing Same Compound, And Hydrate of Same Compound JW PHARMACEUTICAL CORPORATION (KR) 2020-07-02 US disclosed
EP-3632917-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND JW Pharmaceutical Corporation (KR) 2020-04-08 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 (10 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-20220363691-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-20240083911-A1 Method For Preparing Heterocyclic Derivative Compound, Composition Containing Same Compound, And Hydrate of Same Compound REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-12103938-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-20260070923-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND SLC26A3, SLC10A6, SLC14A1 PARP1 3709/4885PDE3B 2540/4885PDE3A 2307/4885
US-20200207784-A1 Method For Preparing Heterocyclic Derivative Compound, Composition Containing Same Compound, And Hydrate of Same Compound REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-20220340594-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-11866448-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-20240067659-A1 METHOD FOR PREPARING HETEROCYCLIC DERIVATIVE COMPOUND, COMPOSITION CONTAINING SAME COMPOUND, AND HYDRATE OF SAME COMPOUND REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-12497410-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885
US-12030895-B2 Method for preparing heterocyclic derivative compound, composition containing same compound, and hydrate of same compound REN, NOD1, NLRP3 PARP1 4501/4885PDE3B 747/4885PDE3A 623/4885

“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.