Hydrochloric Acid

Hydrochloric Acid

SCHEMBL184070

CCOC(=O)C1CCN(Cc2ccccc2)CC1=O.Cl

nearest known ligand 0.58

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 10)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 1/20 0.47
MEN1 O00255 1/20 0.55
KMT2A Q03164 1/20 0.55
ALDH1A1 P00352 4/20 0.55
CCR8 P51685 1/20 0.52
L3MBTL1 Q9Y468 2/20 0.50
ATM Q13315 1/20 0.50
KDM4E B2RXH2 4/20 0.48
MAPT P10636 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.47

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
SCHEMBL184071 0.99 MEN1 (0.56) MEN1KMT2AALDH1A1CCR8L3MBTL1
SCHEMBL5413556 0.92 L3MBTL1 (0.57) MEN1KMT2AALDH1A1CCR8L3MBTL1
Hydrochloric Acid SCHEMBL5779638 0.90 SMN1; SMN2 (0.47) MEN1KMT2AALDH1A1CCR8L3MBTL1
Hydrochloric Acid SCHEMBL1621693 0.89 ALDH1A1 (0.56) MEN1KMT2AALDH1A1CCR8L3MBTL1
Hydrochloric Acid SCHEMBL17611756 0.89 FKBP1A (0.47) MEN1KMT2ASMN1; SMN2SIGMAR1
SCHEMBL5752863 0.88 L3MBTL1 (0.48) MEN1KMT2AALDH1A1CCR8L3MBTL1
Hydrochloric Acid SCHEMBL7189733 0.88 GPR119 (0.45) MEN1KMT2AALDH1A1CCR8L3MBTL1
SCHEMBL1622710 0.88 ALDH1A1 (0.57) MEN1KMT2AALDH1A1CCR8L3MBTL1
Hydrochloric Acid SCHEMBL183705 0.88 ALDH1A1 (0.51) MEN1KMT2AALDH1A1CCR8L3MBTL1
SCHEMBL350213 0.88 FKBP1A (0.47) MEN1KMT2ASMN1; SMN2SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119392325-B Cyanide-free gold plating solution for plating gold on micro blind holes and electroplating method 深圳创智芯联科技股份有限公司 2025-04-01 CN claimed
CN-119392325-A Cyanide-free gold plating solution for plating gold on micro blind holes and electroplating method 深圳创智芯联科技股份有限公司 2025-02-07 CN claimed
CN-110734393-B Preparation method of N-benzyl-3-oxopiperidine-4-carboxylic acid ethyl ester hydrochloride 南京恒远科技开发有限公司 2022-02-25 CN claimed
CN-110734393-A Preparation method of N-benzyl-3-oxopiperidine-4-carboxylic acid ethyl ester hydrochloride 南京恒远科技开发有限公司 2020-01-31 CN claimed
EP-4216951-B1 KRAS G12D INHIBITORS MIRATI THERAPEUTICS INC (US) 2026-04-01 EP disclosed
US-12509438-B2 Pyrazole derivative APTABIO THERAPEUTICS INC. (KR) 2025-12-30 US disclosed
US-20250282778-A1 CRYSTALLINE FORMS OF A KRAS G12C INHIBITOR MIRATI THERAPEUTICS INC (US) 2025-09-11 US disclosed
US-12286431-B2 Crystalline forms of a KRas G12C inhibitor Mirati Therapeutics, Inc. (US) 2025-04-29 US disclosed
US-12281113-B2 Crystalline forms of a KRas G12C inhibitor Mirati Therapeutics, Inc. (US) 2025-04-22 US disclosed
CN-119392325-B Cyanide-free gold plating solution for plating gold on micro blind holes and electroplating method 深圳创智芯联科技股份有限公司 2025-04-01 CN disclosed
CN-119392325-A Cyanide-free gold plating solution for plating gold on micro blind holes and electroplating method 深圳创智芯联科技股份有限公司 2025-02-07 CN disclosed
CN-115348959-B Heteroaryl compounds and their therapeutic use in conditions associated with altered beta-glucocerebrosidase activity GT增益治疗股份有限公司 2025-01-07 CN disclosed
EP-0897303-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE Merck & Co., Inc. (US) 1999-02-24 EP disclosed
EP-0897303-A4 1999-02-24 EP disclosed
WO-1997036605-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO., INC. (US) 1997-10-09 WO disclosed
US-4831029-A SEDATIVES, TRANQUILIZERS REITER JOZSEF (HU) 1989-05-16 US disclosed
CN-87107643-A CONDENSED CYCLIC TRIAZOLE DERIVATIVES 1988-08-24 CN disclosed
US-4254116-A ANALGESICS, ANTIDEPRESSANTS, NEUTRALIZING AGENTS ABBOTT LABORATORIES (US) 1981-03-03 US disclosed
US-RE29196-E ANALGESICS AND TRANQUILIZERS ABBOTT LABORATORIES (US) 1977-04-26 US disclosed
US-3932432-A Alkylphenyl benzopyranopyridines ABBOTT LABORATORIES (US) 1976-01-13 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 (4 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-12281113-B2 Crystalline forms of a KRas G12C inhibitor KRAS, NRAS, HRAS SIGMAR1 4508/4885MEN1 506/4885KMT2A 1138/4885
US-12509438-B2 Pyrazole derivative CBR3, NR3C2, NR3C1 SIGMAR1 153/4885MEN1 3044/4885KMT2A 4419/4885
US-12286431-B2 Crystalline forms of a KRas G12C inhibitor KRAS, NRAS, HRAS SIGMAR1 4508/4885MEN1 506/4885KMT2A 1138/4885
US-20250282778-A1 CRYSTALLINE FORMS OF A KRAS G12C INHIBITOR KRAS, NRAS, HRAS SIGMAR1 4508/4885MEN1 506/4885KMT2A 1138/4885

“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.