Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1368802

Cl.N[C@H](CO)C(=O)OCc1ccccc1

nearest known ligand 0.52

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
SLC6A2 known ✓ P23975 1/20 0.50
SLC6A3 known ✓ Q01959 1/20 0.50
PTGS1 known ✓ P23219 1/20 0.47
ALDH1A1 P00352 4/20 0.52
KMT2A Q03164 2/20 0.50
IDO1 P14902 2/20 0.50
MAPK1 P28482 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
SLC15A1 P46059 1/20 0.48
LTA4H P09960 1/20 0.48
LAP3 P28838 1/20 0.48
SLC1A1 P43005 4/20 0.47
SLC1A3 P43003 3/20 0.47
SLC1A2 P43004 2/20 0.47
MEN1 O00255 1/20 0.47
CYP1A2 P05177 1/20 0.47
CYP2D6 P10635 1/20 0.47
CYP2C9 P11712 1/20 0.47
CYP2C19 P33261 1/20 0.47

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 SCHEMBL543358 1.00 ALDH1A1 (0.52) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
Hydrochloric Acid SCHEMBL3259892 1.00 ALDH1A1 (0.52) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
SCHEMBL218263 0.98 ALDH1A1 (0.53) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
SCHEMBL540214 0.98 ALDH1A1 (0.53) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
SCHEMBL218262 0.98 ALDH1A1 (0.53) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
Trifluoroacetic Acid SCHEMBL27745869 0.89 SLC15A1 (0.46) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
Hydrochloric Acid SCHEMBL2916431 0.86 ALDH1A1 (0.49) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
Hydrochloric Acid SCHEMBL28349108 0.86 ALDH1A1 (0.49) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
Hydrochloric Acid SCHEMBL27309456 0.86 ALDH1A1 (0.49) ALDH1A1KMT2AIDO1MAPK1L3MBTL1
Hydrochloric Acid SCHEMBL27309455 0.86 ALDH1A1 (0.49) ALDH1A1KMT2AIDO1MAPK1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12319660-B2 Preparation of substituted diaminopyrazine dicarboxylic acids MEDIBEACON INC. (US) 2025-06-03 US claimed
EP-4313172-A1 PREPARATION OF SUBSTITUTED DIAMINOPYRAZINE DICARBOXYLIC ACIDS Medibeacon Inc. (US) 2024-02-07 EP claimed
CN-117241839-A Preparation of substituted diaminopyrazine dicarboxylic acids 麦迪贝肯有限公司 2023-12-15 CN claimed
US-20220324818-A1 PREPARATION OF SUBSTITUTED DIAMINOPYRAZINE DICARBOXYLIC ACIDS MEDIBEACON INC. 2022-10-13 US claimed
WO-2022212077-A1 PREPARATION OF SUBSTITUTED DIAMINOPYRAZINE DICARBOXYLIC ACIDS MEDIBEACON INC. (US) 2022-10-06 WO claimed
EP-4019528-B1 BILE ACID DERIVATIVE, COMPOSITION AND APPLICATION THEREOF SHENZHEN YUNHE PHARMACEUTICAL TECH PARTNERSHIP LIMITED (CN) 2026-01-28 EP disclosed
US-12491190-B2 Bile acid derivative, composition and application thereof SHENZHEN YUNHE PHARMACEUTICAL TECHNOLOGY PARTNERSHIP (LIMITED) (CN) 2025-12-09 US disclosed
EP-3700578-B1 SYSTEMS FOR RENAL FUNCTION DETERMINATION MEDIBEACON INC (US) 2025-12-03 EP disclosed
US-12319660-B2 Preparation of substituted diaminopyrazine dicarboxylic acids MEDIBEACON INC. (US) 2025-06-03 US disclosed
CN-114555087-B Anodic oxidation of 5-aminouracil 麦迪贝肯有限公司 2025-04-18 CN disclosed
WO-2025055882-A1 MB-102 RELATED COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 杭州中美华东制药有限公司 2025-03-20 WO disclosed
CN-117769543-A Method for preparing pyrazine carboxylic acid derivatives as fluorescent tracers 杭州中美华东制药有限公司 2024-03-26 CN disclosed
US-6124298-A USED IN REGULATING HAEMATOPOIESIS NYCOMED IMAGING AS (NO) 2000-09-26 US disclosed
EP-0799208-B1 PYRIDINE AND PYRAZINEDICARBOXYLIC-ACID DERIVATIVES AS CELL PROLIFERATION REGULATORS NYCOMED IMAGING AS (NO) 2000-09-13 EP disclosed
US-5972926-A REACTING A DIAMINE DERIVATIVE WITH PYRIDINE OR PYRIZINE 2,3-DICARBOXYLIC ACID OR 2,3-CARBOXYLIC ANHYDRIDE, CONVERTING THE COMPOUND INTO A SALT, RESOLVING THE FORMED COMPOUND INTO ITS ISOMER NYCOMED IMAGING AS (NO) 1999-10-26 US disclosed
US-5925659-A SUBSTITUTED 4-HYDROXAMIDO-2-PHENYL-OXAZOLINES FOR TREATMENT OF GRAMNEGATIVE BACTERIAL INFECTIONS MERCK & CO., INC. (US) 1999-07-20 US disclosed
US-5693772-A PROTECTING ACID AND HYDROXY GROUPS OF BENANOMICIN A, REDUCTION OF AMIDE TO IMIDOESTER WITH MEERWEIN REAGENT, DEPROTECTING, REFLUXING IN ACETONE/WATER MIXTURE TO CLEAVE IMIDOESTER AND FORM CARBOXY GROUP ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1997-12-02 US disclosed
EP-0799208-A1 PYRIDINE AND PYRAZINEDICARBOXYLIC-ACID DERIVATIVES AS CELL PROLIFERATION REGULATORS NYCOMED IMAGING AS (NO) 1997-10-08 EP disclosed
WO-1996019457-A1 PYRIDINE AND PYRAZINEDICARBOXYLIC-ACID DERIVATIVES AS CELL PROLIFERATION REGULATORS NYCOMED IMAGING AS (NO) 1996-06-27 WO disclosed
EP-0684253-A1 DESALANINEBENANOMICIN A DERIVATIVE AND PRODUCTION THEREOF ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1995-11-29 EP 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 (3 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-12319660-B2 Preparation of substituted diaminopyrazine dicarboxylic acids DDC, DPYD, SDHA SLC6A2 992/4885SLC6A3 1571/4885PTGS1 2708/4885
US-20220324818-A1 PREPARATION OF SUBSTITUTED DIAMINOPYRAZINE DICARBOXYLIC ACIDS DDC, DPYD, SDHA SLC6A2 992/4885SLC6A3 1571/4885PTGS1 2708/4885
US-12491190-B2 Bile acid derivative, composition and application thereof NR1H4, GPBAR1, GLP1R SLC6A2 2725/4885SLC6A3 2691/4885PTGS1 1317/4885

“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.