Hydrochloric Acid

Hydrochloric Acid

SCHEMBL27409281

CCCCCCCC(N)=O.Cl

nearest known ligand 0.71

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
PPARG known ✓ P37231 6/20 0.59
HDAC11 known ✓ Q96DB2 5/20 0.59
ESR1 known ✓ P03372 1/20 0.59
PDE4A known ✓ P27815 1/20 0.59
PDE3A known ✓ Q14432 1/20 0.59
SOAT1 P35610 2/20 0.71
MEN1 O00255 2/20 0.71
KMT2A Q03164 2/20 0.71
FAAH O00519 1/20 0.71
TP53 P04637 1/20 0.71
CYP1A2 P05177 1/20 0.71
CYP3A4 P08684 1/20 0.71
CYP2C19 P33261 1/20 0.71
KDM4E B2RXH2 2/20 0.63
CES2 O00748 3/20 0.62
CES1 P23141 3/20 0.62
GPR84 Q9NQS5 7/20 0.59
PPARD Q03181 6/20 0.59
PPARA Q07869 6/20 0.59
TSHR P16473 4/20 0.59

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 SCHEMBL29863502 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Hydrochloric Acid SCHEMBL28977480 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Hydrochloric Acid SCHEMBL30958746 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Hydrochloric Acid SCHEMBL6941901 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Hydrochloric Acid SCHEMBL31367850 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Palmitamide SCHEMBL25349110 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Octadecanoic Acid Amide SCHEMBL5791921 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Tetradecanamide SCHEMBL30958755 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Hydrochloric Acid SCHEMBL30958748 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53
Tetradecanamide SCHEMBL28136606 1.00 SOAT1 (0.71) SOAT1MEN1KMT2AFAAHTP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240425517-A1 NOVEL COMPOUND FOR DEGRADATION OF TARGET PROTEIN OR POLYPEPTIDE BY POLYUBIQUITINATION PRAZER THERAPEUTICS INC. (KR) 2024-12-26 US claimed
CN-103724573-B A kind of preparation method of amphipathic copolymerization network DONGHUA UNIVERSITY (CN) 2016-01-20 CN claimed
CN-103865067-B A kind of preparation method of amphipathic copolymerization network DONGHUA UNIVERSITY (CN) 2016-01-06 CN claimed
CN-104592532-A Amphiphilic copolymer network and preparation method thereof NAT UNIV DONG HWA 2015-05-06 CN claimed
CN-103865067-A Method for preparing amphiphilic copolymeric network UNIV DONGHUA 2014-06-18 CN claimed
CN-103724573-A Method for preparing amphipathic copolymerization network UNIV DONGHUA 2014-04-16 CN claimed
US-20240425517-A1 NOVEL COMPOUND FOR DEGRADATION OF TARGET PROTEIN OR POLYPEPTIDE BY POLYUBIQUITINATION PRAZER THERAPEUTICS INC. (KR) 2024-12-26 US disclosed
CN-116437913-A Pharmaceutical compounds for treating complement-mediated disorders 艾其林医药公司 2023-07-14 CN disclosed
CN-113717161-B Nitrogen-containing saturated heterocyclic compound, preparation method thereof, pharmaceutical composition and application 广州费米子科技有限责任公司 2023-06-09 CN disclosed
CN-114685505-A Imidazopyrrolopyridines as JAK family kinase inhibitors 詹森药业有限公司 2022-07-01 CN disclosed
CN-110312719-B Imidazopyrrolopyridines as JAK family kinase inhibitors 詹森药业有限公司 2022-04-15 CN disclosed
CN-113717161-A Nitrogen-containing saturated heterocyclic compound and preparation method, pharmaceutical composition and application thereof 广州费米子科技有限责任公司 2021-11-30 CN disclosed
CN-113226296-A SSAO inhibitors and uses thereof 梅塔科林公司 2021-08-06 CN disclosed
CN-101351443-A Process for preparing sulfonamides BASF AG (DE) 2009-01-21 CN disclosed
CN-101218218-A Novel Pyrocatechol Derivatives NOVARTIS AG (CH) 2008-07-09 CN disclosed
CN-1839194-A Treatment of crude oil fractions, fossil fuels and products thereof MARK CULLEN (US) 2006-09-27 CN disclosed
CN-1169791-C Novel acetamide derivatives and protease inhibitors �ձ���ҩ��ʽ���� 2004-10-06 CN disclosed
CN-1312805-A Benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake SEARLE & CO (US) 2001-09-12 CN disclosed
CN-1229405-A Novel acetamide derivatives and protease inhibitors NIPPON KAYAKU KK (JP) 1999-09-22 CN disclosed
CN-1100734-A Process for producing cross-linked monodispersed polymeric particles GEN ELECTRIC (US) 1995-03-29 CN 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-20240425517-A1 NOVEL COMPOUND FOR DEGRADATION OF TARGET PROTEIN OR POLYPEPTIDE BY POLYUBIQUITINATION ADRM1, SUMO1, SUMO2 PPARG 3040/4885HDAC11 1761/4885ESR1 2938/4885

“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.