Hydrochloric Acid

Hydrochloric Acid

SCHEMBL227522

CC(C)N(CCCl)C(C)C.Cl

nearest known ligand 0.94

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 9)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.94
KMT2A Q03164 1/20 0.94
LMNA P02545 2/20 0.45
TP53 P04637 1/20 0.45
TSHR P16473 1/20 0.45
HTT P42858 1/20 0.45
HBB P68871 1/20 0.45
MAPT P10636 1/20 0.40
ALDH1A1 P00352 1/20 0.33

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
SCHEMBL2990827 0.97 MEN1 (1.00) MEN1KMT2ALMNATP53TSHR
SCHEMBL226273 0.97 MEN1 (1.00) MEN1KMT2ALMNATP53TSHR
Phosphine SCHEMBL27652671 0.94 MEN1 (0.94) MEN1KMT2ALMNATP53TSHR
SCHEMBL27834982 0.94 MEN1 (0.94) MEN1KMT2ALMNATP53TSHR
Hydrochloric Acid SCHEMBL28047633 0.91 MEN1 (0.88) MEN1KMT2ALMNATP53TSHR
SCHEMBL28125636 0.91 MEN1 (0.88) MEN1KMT2ALMNATP53TSHR
Hydrochloric Acid SCHEMBL8950200 0.89 MEN1 (0.75) MEN1KMT2ALMNATP53TSHR
Tert-Butylamine SCHEMBL9152840 0.87 MEN1 (0.71) MEN1KMT2ALMNATP53TSHR
Hydrochloric Acid SCHEMBL9492390 0.82 MEN1 (0.65) MEN1KMT2ALMNATP53TSHR
SCHEMBL8997704 0.82 MEN1 (0.71) MEN1KMT2ALMNATP53TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240216531-A1 CHITOSAN-CONTAINING NANOPARTICLES FOR DELIVERY OF POLYNUCLEOTIDES VALORISATION RECH HSCM LIMITED PARTNERSHIP (CA) 2024-07-04 US claimed
CN-113292440-A Preparation method of N, N-diisopropylethylenediamine and preparation method of pramiperacetam monohydrate 浙江朗华制药有限公司 2021-08-24 CN claimed
CN-112225626-A High-nutrient organic fertilizer prepared from livestock and poultry manure 安徽正基生态农业有限公司 2021-01-15 CN claimed
CN-106365243-B Abandon a class type rainwater deep cycle purifier and purification process thereof 徐州工程学院 2020-09-08 CN claimed
CN-104341333-B A kind of preparation method of pramiracetam sulfate BEIJING HUARUI DINGXIN TECHNOLOGY CO., LTD. (CN) 2016-03-02 CN claimed
CN-104341333-A Preparation method of Pramiracetam sulfate BEIJING HRDX MEDICINAL TECHNOLOGIES CO LTD 2015-02-11 CN claimed
CN-101058542-B [2-(2-Diisopropylamino-ethylamino)-ethyl]-diisopropyl-amine, and synthetic method and use thereof UNIV ZHEJIANG 2010-10-06 CN claimed
CN-101058542-A [2-(2-Diisopropylamino-ethylamino)-ethyl]-diisopropyl-amine, and synthetic method and use thereof UNIV ZHEJIANG (CN) 2007-10-24 CN claimed
US-12398097-B2 WDR5-MYC inhibitors VANDERBILT UNIVERSITY (US) 2025-08-26 US disclosed
US-20240216531-A1 CHITOSAN-CONTAINING NANOPARTICLES FOR DELIVERY OF POLYNUCLEOTIDES VALORISATION RECH HSCM LIMITED PARTNERSHIP (CA) 2024-07-04 US disclosed
US-11685761-B2 Cyclic di-nucleotide compounds as sting agonists MERCK SHARP & DOHME LLC (US) 2023-06-27 US disclosed
CN-115991653-A Preparation method of prazoracetam key intermediate N, N-diisopropyl ethylenediamine 河南省三生药业有限公司 2023-04-21 CN disclosed
US-20220289673-A1 WDR5-MYC INHIBITORS VANDERBILT UNIVERSITY 2022-09-15 US disclosed
US-11420963-B2 Rebamipide prodrugs, preparation method and use thereof SAMJIN PHARMACEUTICAL CO., LTD. (KR) 2022-08-23 US disclosed
US-4144338-A N-pyrimidinyl-N-dialkylaminoalkyl ureas MERCK & CO., INC. (US) 1979-03-13 US disclosed
US-4113951-A ANTIARRHYTHMIA DELALANDE S. A. (FR) 1978-09-12 US disclosed
US-4105849-A [(Substituted )phenyl]phenylmethyl-1-(dialkylaminoalkyl)piperidines G. D. SEARLE & CO. (US) 1978-08-08 US disclosed
US-4073917-A Local anesthetics tertiary aminoalkoxyphenyl ethers ASTRA LAKEMEDEL AKTIEBOLAG (SW) 1978-02-14 US disclosed
US-4009201-A PARTIALLY OR FULLY QUATERNIZED POLYAMINE ESTERS OF ACRYLIC ACIDS ALCOLAC INC. (US) 1977-02-22 US disclosed
US-3953602-A DELAYED HYPERSENSITIVITY RICHARDSON-MERRELL INC. (US) 1976-04-27 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 (5 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-20220289673-A1 WDR5-MYC INHIBITORS MYC, WDR5, MYCBP MEN1 1279/4885KMT2A 186/4885LMNA 2680/4885
US-20240216531-A1 CHITOSAN-CONTAINING NANOPARTICLES FOR DELIVERY OF POLYNUCLEOTIDES TLR3, PCNP, H1-3 MEN1 1339/4885KMT2A 2581/4885LMNA 425/4885
US-12398097-B2 WDR5-MYC inhibitors MYC, WDR5, MYCBP MEN1 1279/4885KMT2A 186/4885LMNA 2680/4885
US-11420963-B2 Rebamipide prodrugs, preparation method and use thereof SI, CYP2A7, MLN MEN1 2774/4885KMT2A 4445/4885LMNA 4782/4885
US-11685761-B2 Cyclic di-nucleotide compounds as sting agonists STING1, CGAS, IFNAR1 MEN1 1971/4885KMT2A 2880/4885LMNA 1653/4885

“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.