Hydrochloric Acid

Hydrochloric Acid

SCHEMBL219232

CCCCCCCC(=O)C(N)(C(=O)CCCCCCC)C(=O)CCCCCCC.Cl

nearest known ligand 0.59

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 5/20 0.50
HDAC11 known ✓ Q96DB2 4/20 0.50
ESR1 known ✓ P03372 1/20 0.50
PDE4A known ✓ P27815 1/20 0.50
PDE3A known ✓ Q14432 1/20 0.50
FAAH O00519 8/20 0.59
CES1 P23141 8/20 0.59
CES2 O00748 5/20 0.59
MEN1 O00255 2/20 0.59
KMT2A Q03164 2/20 0.59
HSD17B10 Q99714 2/20 0.59
CYP1A2 P05177 1/20 0.59
PPARD Q03181 5/20 0.50
PPARA Q07869 5/20 0.50
TSHR P16473 3/20 0.50
GPR84 Q9NQS5 3/20 0.50
ALDH1A1 P00352 2/20 0.50
TLR2 O60603 2/20 0.50
TDP1 Q9NUW8 2/20 0.50
FABP4 P15090 2/20 0.50

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 SCHEMBL196410 1.00 FAAH (0.59) FAAHCES1CES2MEN1KMT2A
SCHEMBL2573096 0.98 FAAH (0.61) FAAHCES1CES2MEN1KMT2A
Hydrochloric Acid SCHEMBL9458888 0.98 FAAH (0.58) FAAHCES1CES2MEN1KMT2A
SCHEMBL638951 0.98 FAAH (0.61) FAAHCES1CES2MEN1KMT2A
Bromide SCHEMBL1244460 0.95 FAAH (0.59) FAAHCES1CES2MEN1KMT2A
Water SCHEMBL3120172 0.95 FAAH (0.59) FAAHCES1CES2MEN1KMT2A
Water SCHEMBL11595702 0.95 FAAH (0.59) FAAHCES1CES2MEN1KMT2A
Fluoride SCHEMBL10493503 0.95 FAAH (0.59) FAAHCES1CES2MEN1KMT2A
Iodide SCHEMBL8433341 0.95 FAAH (0.59) FAAHCES1CES2MEN1KMT2A
Bromide SCHEMBL6552300 0.95 FAAH (0.59) FAAHCES1CES2MEN1KMT2A

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 1443 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025074340-A1 A PROCESS FOR PREPARATION OF AMINOBIPHENYL COMPOUNDS AND INTERMEDIATES THEREOF UPL LIMITED (IN) 2025-04-10 WO claimed
WO-2024189550-A1 PROCESS FOR THE PREPARATION OF ISAVUCONAZONIUM SULFATE AND ITS CRYSTALLINE FORMS APITORIA PHARMA PRIVATE LIMITED (IN) 2024-09-19 WO claimed
US-20240057934-A1 WEARABLE DEVICE FOR DETECTION OF AMNIOTIC FLUID SAVYON DIAGNOSTICS LTD (IL) 2024-02-22 US claimed
EP-4277584-A1 WEARABLE DEVICE FOR DETECTION OF AMNIOTIC FLUID Peptonic Medical Israel Ltd (IL) 2023-11-22 EP claimed
WO-2022153291-A1 WEARABLE DEVICE FOR DETECTION OF AMNIOTIC FLUID PEPTONIC MEDICAL ISRAEL LTD (IL) 2022-07-21 WO claimed
US-11135338-B2 Diagnostic composition for identifying amniotic fluid COMMON SENSE LTD. (US) 2021-10-05 US claimed
US-20190240373-A1 DIAGNOSTIC COMPOSITION FOR IDENTIFYING AMNIOTIC FLUID COMMON SENSE LTD. 2019-08-08 US claimed
US-10265692-B2 Ex vivo methods for predicting and confirming in vivo metabolism of pharmaceutically active compounds EMPIRIKO CORPORATION (US) 2019-04-23 US claimed
US-9981898-B1 Process for oxidation of fatty alkenols to alkenal pheromone products PROVIVI, INC. (US) 2018-05-29 US claimed
US-20160303553-A1 EX VIVO METHODS FOR PREDICTING AND CONFIRMING IN VIVO METABOLISM OF PHARMACEUTICALLY ACTIVE COMPOUNDS EMPIRIKO CORPORATION 2016-10-20 US claimed
US-4626288-A Starch derivatives forming reversible gels NATIONAL STARCH AND CHEMICAL CORPORATION (US) 1986-12-02 US claimed
EP-0188237-A1 Reversible gels of starch derivatives National Starch and Chemical Corporation (US) 1986-07-23 EP claimed
US-4539422-A Process for preparing cephalosporin intermediates ELI LILLY AND COMPANY (US) 1985-09-03 US claimed
EP-0136145-A2 Process for preparing alkyl cyanoformates ELI LILLY AND COMPANY (US) 1985-04-03 EP claimed
US-4422970-A ALKYLATION OF AZACYCLOHEPTAN-2-ONE, QUATERNARY AMMONIUM PHASE TRANSFER CATALYST NELSON RESEARCH & DEVELOPMENT COMPANY (US) 1983-12-27 US claimed
EP-0095096-A2 Improved method of synthesis of 1-substituted azacycloalkan-2-ones Whitby Research Incorporated (US) 1983-11-30 EP claimed
US-4359429-A Mercaptoacetonitrile synthesis W. R. GRACE & CO. (US) 1982-11-16 US claimed
US-4304929-A Process for preparing 4-(n-hexadecylamino)-benzoic acid LEK TOVARNA FARMACEVTSKIH IN KEMICNIH IZDELKOV, N.SOL.O. (YU) 1981-12-08 US claimed
US-4225428-A USING QUATERNARY AMMONIUM CHLORIDE AND PERCHLORIC ACID PETROVICH VOJISLAV 1980-09-30 US claimed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20160303553-A1 EX VIVO METHODS FOR PREDICTING AND CONFIRMING IN VIVO METABOLISM OF PHARMACEUTICALLY ACTIVE COMPOUNDS CYP3A43, CYP3A4, CYP2D6 PPARG 769/4885HDAC11 778/4885ESR1 2251/4885
US-10265692-B2 Ex vivo methods for predicting and confirming in vivo metabolism of pharmaceutically active compounds CYP3A43, CYP3A4, CYP2D6 PPARG 769/4885HDAC11 778/4885ESR1 2251/4885

“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.