Hydrochloric Acid

Hydrochloric Acid

SCHEMBL22033461

CC1(N)CCN(c2cnc(-c3cccc(Cl)c3Cl)c(N)n2)CC1.Cl.Cl

nearest known ligand 0.98

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 4)

geneUniProtsupporting neighboursconfidence
KCNH2 known ✓ Q12809 2/20 0.98
PTPN11 Q06124 20/20 0.98
MAPK3 P27361 1/20 0.98
MAPK1 P28482 1/20 0.98

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 SCHEMBL29479127 1.00 PTPN11 (0.98) PTPN11KCNH2MAPK3MAPK1
Hydrochloric Acid SCHEMBL29828013 1.00 PTPN11 (0.98) PTPN11KCNH2MAPK3MAPK1
Hydrochloric Acid SCHEMBL29024442 1.00 PTPN11 (0.98) PTPN11KCNH2MAPK3MAPK1
SCHEMBL16914284 0.99 PTPN11 (1.00) PTPN11KCNH2MAPK3MAPK1
SCHEMBL29352400 0.99 PTPN11 (1.00) PTPN11KCNH2MAPK3MAPK1
SCHEMBL26247011 0.91 PTPN11 (0.85) PTPN11KCNH2MAPK3MAPK1
SCHEMBL26015655 0.89 PTPN11 (0.82) PTPN11KCNH2MAPK3MAPK1
SCHEMBL30295870 0.88 PTPN11 (0.80) PTPN11KCNH2MAPK3MAPK1
SCHEMBL19785300 0.88 PTPN11 (0.80) PTPN11KCNH2MAPK3MAPK1
SCHEMBL25485425 0.87 PTPN11 (0.78) PTPN11KCNH2MAPK3MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240423984-A1 COMBINATION THERAPIES OF KRAS G12D INHIBITORS WITH SHP-2 INHIBITORS MIRATI THERAPEUTICS, INC 2024-12-26 US claimed
US-20220079947-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. 2022-03-17 US claimed
US-20210113659-A1 ENGINEERED THERAPEUTIC TO ENHANCE CYTOTOXIC ACTIVITY AND PHAGOCYTOSIS IN TUMOR ASSOCIATED MACROPHAGES UNIVERSITY OF MASSACHUSETTS 2021-04-22 US claimed
US-20250340548-A1 KRAS G12C INHIBITORS FRONTIER MEDICINES CORP (US) 2025-11-06 US disclosed
US-12377101-B2 Combination therapies Mirati Therapeutics, Inc. (US) 2025-08-05 US disclosed
WO-2025106901-A1 COMBINATION CANCER THERAPIES WITH A KRAS MODULATOR AND AN RTK-MAPK PATHWAY INHIBITOR QUANTA THERAPEUTICS, INC. (US) 2025-05-22 WO disclosed
US-12291539-B2 KRAS G12C inhibitors FRONTIER MEDICINES CORPORATION (US) 2025-05-06 US disclosed
US-20250129103-A1 METHODS FOR TREATMENT OF CANCER FRONTIER MEDICINES CORPORATION 2025-04-24 US disclosed
US-20250019387-A1 KRAS G12C INHIBITORS FRONTIER MEDICINES CORPORATION 2025-01-16 US disclosed
US-20240423984-A1 COMBINATION THERAPIES OF KRAS G12D INHIBITORS WITH SHP-2 INHIBITORS MIRATI THERAPEUTICS, INC 2024-12-26 US disclosed
US-20240417412-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE AMGEN INC. (US) 2024-12-19 US disclosed
CN-117835976-A Heterocyclic compounds and methods of use 安进公司 2024-04-05 CN disclosed
CN-117651700-A 2-aminobenzothiazole compounds and methods of use 安进公司 2024-03-05 CN disclosed
CN-117561063-A Heterocyclic compounds and methods of use 安进公司 2024-02-13 CN disclosed
WO-2023150394-A1 METHODS FOR TREATMENT OF CANCER FRONTIER MEDICINES CORPORATION (US) 2023-08-10 WO disclosed
WO-2023081840-A1 KRAS G12C INHIBITORS FRONTIER MEDICINES CORPORATION (US) 2023-05-11 WO disclosed
US-20220079947-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. 2022-03-17 US disclosed
EP-3890716-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2021-10-13 EP disclosed
US-20210113659-A1 ENGINEERED THERAPEUTIC TO ENHANCE CYTOTOXIC ACTIVITY AND PHAGOCYTOSIS IN TUMOR ASSOCIATED MACROPHAGES UNIVERSITY OF MASSACHUSETTS 2021-04-22 US disclosed
WO-2020118066-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2020-06-11 WO 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 (8 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-20240423984-A1 COMBINATION THERAPIES OF KRAS G12D INHIBITORS WITH SHP-2 INHIBITORS KRAS, NRAS, SHPRH KCNH2 4609/4885PTPN11 24/4885MAPK3 765/4885
US-20240417412-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE KRAS, NRAS, HRAS KCNH2 4325/4885PTPN11 551/4885MAPK3 554/4885
US-12291539-B2 KRAS G12C inhibitors KRAS, NRAS, HRAS KCNH2 4645/4885PTPN11 583/4885MAPK3 525/4885
US-20250129103-A1 METHODS FOR TREATMENT OF CANCER KRAS, HRAS, TP53 KCNH2 4760/4885PTPN11 1658/4885MAPK3 2082/4885
US-20250340548-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS KCNH2 4645/4885PTPN11 583/4885MAPK3 525/4885
US-20220079947-A1 COMBINATION THERAPIES KRAS, NRAS, HRAS KCNH2 4389/4885PTPN11 9/4885MAPK3 1039/4885
US-12377101-B2 Combination therapies KRAS, NRAS, HRAS KCNH2 4389/4885PTPN11 9/4885MAPK3 1039/4885
US-20250019387-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS KCNH2 4645/4885PTPN11 583/4885MAPK3 525/4885

“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.