Hydrochloric Acid

Hydrochloric Acid

SCHEMBL25242562

Cl.NC(=O)c1cncnc1

nearest known ligand 0.56

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
PARP1 known ✓ P09874 1/20 0.40
ADRA1A known ✓ P35348 1/20 0.38
HCAR2 Q8TDS4 1/20 0.56
SIRT2 Q8IXJ6 2/20 0.52
SIRT1 Q96EB6 2/20 0.52
SIRT3 Q9NTG7 2/20 0.52
F7 P08709 1/20 0.52
F3 P13726 1/20 0.52
SARM1 Q6SZW1 1/20 0.52
SIRT6 Q8N6T7 1/20 0.52
SIRT5 Q9NXA8 1/20 0.52
SIRT4 Q9Y6E7 1/20 0.52
AR P10275 1/20 0.43
NNMT P40261 3/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
MKNK1 Q9BUB5 6/20 0.41
MKNK2 Q9HBH9 6/20 0.41
TSHR P16473 2/20 0.40
POLB P06746 1/20 0.40
CYP3A4 P08684 1/20 0.40

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 SCHEMBL12971394 1.00 HCAR2 (0.56) HCAR2SIRT2SIRT1SIRT3F7
Hydrochloric Acid SCHEMBL28749975 0.97 HCAR2 (0.54) HCAR2SIRT2SIRT1SIRT3F7
SCHEMBL503242 0.97
SCHEMBL27541990 0.95
SCHEMBL27941587 0.95 HCAR2 (0.56) HCAR2SIRT2SIRT1SIRT3F7
SCHEMBL28147137 0.95 HCAR2 (0.56) HCAR2SIRT2SIRT1SIRT3F7
Water SCHEMBL27583249 0.95 HCAR2 (0.56) HCAR2SIRT2SIRT1SIRT3F7
Sulfuric Acid SCHEMBL27952916 0.88 HCAR2 (0.50) HCAR2SIRT2SIRT1SIRT3F7
Formic Acid SCHEMBL25244373 0.88 HCAR2 (0.50) HCAR2SIRT2SIRT1SIRT3F7
SCHEMBL27941661 0.84 HCAR2 (0.46) HCAR2SIRT2SIRT1SIRT3F7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4565585-A1 COMPOUNDS FOR MODULATING RET PROTEIN Bristol-Myers Squibb Company (US) 2025-06-11 EP disclosed
EP-4441042-A1 5-PYRIMIDINECARBOXAMIDE DERIVATIVES AND METHODS OF USING THE SAME Rgenta Therapeutics, Inc. (US) 2024-10-09 EP disclosed
CN-118251389-A Pyridyl derivatives as sodium channel activators 泽农医药公司 2024-06-25 CN disclosed
CN-115594666-B Synthesis and application of phosphatase degradation agent 海创药业股份有限公司 2024-05-31 CN disclosed
CN-117586253-A Protein degradation agent, preparation method thereof and application thereof in pharmacy 上海汇伦医药股份有限公司 2024-02-23 CN disclosed
WO-2024032529-A1 PROTEIN DEGRADATION AGENT AND PREPARATION METHOD THEREFOR AND PHARMACEUTICAL USE THEREOF 上海汇伦医药股份有限公司 2024-02-15 WO disclosed
US-20240041783-A1 AGGREGATING MICROPARTICLES FOR MEDICAL THERAPY Graybug Vision, Inc. (US) 2024-02-08 US disclosed
WO-2024030968-A1 COMPOUNDS FOR MODULATING RET PROTEIN BRYSTOL-MYERS SQUIBB COMPANY (US) 2024-02-08 WO disclosed
WO-2023165943-A1 3-ALKYNYL CARBOXAMIDES AS AEP MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2023-09-07 WO disclosed
CN-111892577-B Compounds and methods for androgen receptor targeted degradation 阿尔维纳斯运营股份有限公司 2023-07-07 CN disclosed
CN-107847763-A Targeted selection of patients eligible for treatment with cortistatin derivatives 哈佛学院院长等 2018-03-27 CN disclosed
CN-106946795-A Substituted dicarbamylamine and diaminourea formonitrile HCN pyrimidine, its composition, and the method treated with it 西格诺药品有限公司 2017-07-14 CN disclosed
CN-103608018-B Use of substituted 2, 3-dihydroimidazo [1,2-C ] quinazolines 拜耳知识产权有限责任公司 2017-06-30 CN disclosed
CN-103492370-B Substituted diaminocarboxamides and diaminocarbonitrile pyrimidines, compositions thereof, and methods of treatment therewith 西格诺药品有限公司 2016-10-26 CN disclosed
CN-103608018-A Use of substituted 2, 3-dihydroimidazo [1,2-C ] quinazolines Bayer Pharma AG 2014-02-26 CN disclosed
CN-101163696-B Histone deacetylase inhibitors CHROMA THERAPEUTICS LTD 2011-09-14 CN disclosed
CN-101321751-A Met kinase inhibitors BRISTOL MYERS SQUIBB CO (US) 2008-12-10 CN disclosed
CN-101163696-A Histone deacetylase inhibitors CHROMA THERAPEUTICS LTD (GB) 2008-04-16 CN disclosed
CN-1330654-C Fused bicyclic pyrimidine derivatives KYORIN SEIYAKU KK (JP) 2007-08-08 CN disclosed
CN-1656098-A Fused bicyclic pyrimidine derivatives KYORIN SEIYAKU KK (JP) 2005-08-17 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-20240041783-A1 AGGREGATING MICROPARTICLES FOR MEDICAL THERAPY MIF, VEGFA, ICAM1 PARP1 3225/4885ADRA1A 1380/4885HCAR2 1309/4885

“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.