Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4295557

Cl.Cl.Nc1cc(N)cc(C(=O)O)c1

nearest known ligand 0.54

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
CA2 known ✓ P00918 2/20 0.48
DPP4 known ✓ P27487 1/20 0.46
TTR known ✓ P02766 2/20 0.42
GABRP known ✓ O00591 1/20 0.41
GABRD known ✓ O14764 1/20 0.41
GABRA1 known ✓ P14867 1/20 0.41
GABRB1 known ✓ P18505 1/20 0.41
GABRG2 known ✓ P18507 1/20 0.41
GABRB3 known ✓ P28472 1/20 0.41
GABRA5 known ✓ P31644 1/20 0.41
GABRA3 known ✓ P34903 1/20 0.41
GABRA2 known ✓ P47869 1/20 0.41
GABRB2 known ✓ P47870 1/20 0.41
GABRA4 known ✓ P48169 1/20 0.41
GABRE known ✓ P78334 1/20 0.41
GABRA6 known ✓ Q16445 1/20 0.41
GABRG1 known ✓ Q8N1C3 1/20 0.41
GABRG3 known ✓ Q99928 1/20 0.41
GABRQ known ✓ Q9UN88 1/20 0.41
LCK known ✓ P06239 1/20 0.41

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 SCHEMBL2810739 1.00 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
SCHEMBL109155 0.97 KDM4E (0.56) KDM4EMEN1KMT2AALDH1A1LMNA
SCHEMBL1478628 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
SCHEMBL2888306 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
Ammonia Solution, Strong SCHEMBL9859476 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
Hydrochloric Acid SCHEMBL9311860 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
Water SCHEMBL2806532 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
Hydrochloric Acid SCHEMBL8653192 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
SCHEMBL1477467 0.94 KDM4E (0.54) KDM4EMEN1KMT2AALDH1A1LMNA
Ethylene SCHEMBL29067611 0.92 KDM4E (0.52) KDM4EMEN1KMT2AALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2000065-A None JP disclosed
CN-119955767-A In vitro reconstitution of the calvin cycle system 中国科学院遗传与发育生物学研究所 2025-05-09 CN disclosed
EP-4549472-A2 COMPOSITIONS FOR SUNSCREEN COMPOUNDS AND METHODS THEREOF PMIDG, LLC (US) 2025-05-07 EP disclosed
EP-4013374-B1 COMPOSITIONS FOR SUNSCREEN COMPOUNDS AND METHODS THEREOF PMIDG LLC (US) 2025-02-19 EP disclosed
CN-118948676-A Compositions for sunscreen compounds and methods thereof 普米戴格有限公司 2024-11-15 CN disclosed
CN-118593387-A Compositions for sunscreen compounds and methods thereof 普米戴格有限公司 2024-09-06 CN disclosed
US-11873389-B2 Composition and molded article AKITA UNIVERSITY (JP) 2024-01-16 US disclosed
CN-113195625-B Composition and molded article 国立大学法人秋田大学 2023-05-02 CN disclosed
US-20220296485-A1 COMPOSITIONS FOR SUNSCREEN COMPOUNDS AND METHODS THEREOF PMIDG, LLC 2022-09-22 US disclosed
EP-4013374-A1 COMPOSITIONS FOR SUNSCREEN COMPOUNDS AND METHODS THEREOF PMIDG, LLC (US) 2022-06-22 EP disclosed
US-5672696-A HEATING DEPARAFFINIZED TISSUE SAMPLE IN PROTEIN-DENATURING AQUEOUS SUSPENSION CONTAINING SURFACTANT, THEN TREATING SUSPENSION WITH PROTEASE AND MIXING WITH SOLUTION OF HYDROXYBENZOIC ACID WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 1997-09-30 US disclosed
WO-1997008145-A1 META-GUANIDINE, UREA, THIOUREA OR AZACYCLIC AMINO BENZOIC ACID DERIVATIVES AS INTEGRIN ANTAGONISTS G.D. SEARLE & CO. (US) 1997-03-06 WO disclosed
US-5602277-A Substituted benzene derivatives useful as neuraminidase inhibitors BIOCRYST PHARMACEUTICALS, INC. (US) 1997-02-11 US disclosed
WO-1996030329-A1 SUBSTITUTED BENZENE DERIVATIVES USEFUL AS NEURAMINIDASE INHIBITORS BIOCRYST PHARMACEUTICALS, INCORPORATED (US) 1996-10-03 WO disclosed
US-5514676-A TO INHIBIT THE FORMATION OF ADVANCED GLYCOSLYATION PRODUCTS BY THE NONENZYMATIC CROSSLINKING OF PROTEINS WITH REDUCING SUGARS, USED IN FOOD PRESERVATION AND TO PREVENT PROTEIN AGING IN COLLAGEN OR LENSES IN THE EYE PRESERVATION THE ROCKEFELLER UNIVERSITY (US) 1996-05-07 US disclosed
EP-0692533-A1 Treatment of paraffin embedded tissue for gene analysis WAKO PURE CHEMICAL INDUSTRIES LTD (JP) 1996-01-17 EP disclosed
EP-0368474-B1 Enhanced amperometric sensor MEDISENSE INC (US) 1995-12-13 EP disclosed
US-5264106-A Enhanced amperometric sensor MEDISENSE, INC. (US) 1993-11-23 US disclosed
EP-0368474-A2 Enhanced amperometric sensor MediSense, Inc. (US) 1990-05-16 EP disclosed
JP-H0265-A PRODUCTION OF PHOTOSENSITIVE RESIN CAPABLE OF DEVELOPING WITH WATER-BASED SOLVENT TOKYO METROPOLIS 1990-01-05 JP 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-20220296485-A1 COMPOSITIONS FOR SUNSCREEN COMPOUNDS AND METHODS THEREOF NQO1, XPA, ERCC1 CA2 4032/4885DPP4 4166/4885TTR 948/4885

“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.