Hydrochloric Acid

Hydrochloric Acid

SCHEMBL196410

CCCCCCCCCC(=O)C(N)(C(=O)CCCCCCCCC)C(=O)CCCCCCCCC.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 SCHEMBL219232 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 1088 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260055219-A1 ULTRA-LOW LOSS HYDROCARBON RESIN COMPOSITION HUNTSMAN ADV MAT SWITZERLAND (CH) 2026-02-26 US claimed
EP-4577590-A1 ULTRA-LOW LOSS HYDROCARBON RESIN COMPOSITION Huntsman Advanced Materials (Switzerland) GmbH (CH) 2025-07-02 EP claimed
WO-2025111580-A1 METHOD AND APPARATUS FOR EXTRACTION OF LITHIUM FROM LITHIUM-CONTAINING CERAMICS Austin Elements, Inc. (US) 2025-05-30 WO claimed
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 US claimed
US-20250066968-A1 METHOD FOR DEGUMMING AND DECOLORIZING POLYESTER FABRIC NAN YA PLASTICS CORPORATION (TW) 2025-02-27 US claimed
WO-2024041995-A1 ULTRA-LOW LOSS HYDROCARBON RESIN COMPOSITION HUNTSMAN ADVANCED MATERIALS LICENSING (SWITZERLAND) GMBH (CH) 2024-02-29 WO claimed
EP-4149886-A1 METHOD FOR PRODUCING BATTERY GRADE LITHIUM HYDROXIDE MONOHYDRATE Katholieke Universiteit Leuven, KU Leuven R&D (BE) 2023-03-22 EP claimed
EP-3257871-B1 METHOD FOR REDUCING OLEFIN OLIGOMERIZATION BYPRODUCT USING A DEACTIVATING AGENT LG CHEMICAL LTD (KR) 2022-08-31 EP claimed
WO-2021228936-A1 METHOD FOR PRODUCING BATTERY GRADE LITHIUM HYDROXIDE MONOHYDRATE KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2021-11-18 WO claimed
EP-3288923-B1 METHOD FOR PREPARING 5-FLUORO-1H-PYRAZOLE-4-CARBONYL FLUORIDES BAYER CROPSCIENCE AG (DE) 2020-02-12 EP claimed
EP-0145377-A2 Process for preparing 3,4'-Amino-Nitro-Diphenylether Montedison S.p.A. (IT) 1985-06-19 EP claimed
EP-0045088-B1 PROCESS FOR PREPARING SUBSTITUTED P-CHLOROPHENYL ALIPHATIC NITRILES STAUFFER CHEMICAL COMPANY (US) 1984-06-20 EP claimed
US-4419524-A Process for the preparation of dihalovinylcyclopropanecarboxylic acids CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT (HU) 1983-12-06 US claimed
US-4418229-A DISPLACEMENT OF CHLORONITROBENZENES WITH A FLUORIDE SALT, QUATERNARY AMMONIUM PHASE TRANSFER CATALYSTS MALLINCKRODT, INC. (US) 1983-11-29 US claimed
EP-0045088-A1 Process for preparing substituted p-chlorophenyl aliphatic nitriles STAUFFER CHEMICAL COMPANY (US) 1982-02-03 EP claimed
US-4277318-A BIPHASIC AQUEOUS-ORGANIC SOLVENT SYSTEM, PHASE TRANSFER CATALYST, MANGANESE COMPOUND IN DIVIDED CELL UNION CARBIDE CORPORATION (US) 1981-07-07 US claimed
US-4191702-A PHASE TRANSFER AGENT ELF UNION (FR) 1980-03-04 US claimed
US-4115512-A SOLUTION OF TRIBUTYL PHOSPHATE AND QUATERNARY AMMONIUM REAGENT NORANDA MINES LIMITED (CA) 1978-09-19 US claimed
US-4082727-A ISOCYANATE-SILOXANE, HEPARIN AGENCY OF INDUSTRIAL SCIENCE & TECHNOLOGY (JA) 1978-04-04 US claimed
US-4067882-A REACTING DIALKOXY-PHOSPHINYL-DITHIOCARBAMATE WITH METHYLENE HALIDE AMERICAN CYANAMID COMPANY (US) 1978-01-10 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 (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-20260055219-A1 ULTRA-LOW LOSS HYDROCARBON RESIN COMPOSITION GTF2E2, UBE2L3, UFL1 PPARG 2221/4885HDAC11 1531/4885ESR1 779/4885

“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.