Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2263936

Cc1ccccc1C1=CCN(C)CC1.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 12)

geneUniProtsupporting neighboursconfidence
HTR1A known ✓ P08908 1/20 0.55
SLC6A4 known ✓ P31645 1/20 0.55
HTR6 known ✓ P50406 1/20 0.55
DRD2 known ✓ P14416 8/20 0.55
DRD4 known ✓ P21917 8/20 0.55
KDM4E B2RXH2 1/20 0.55
LMNA P02545 1/20 0.55
POLB P06746 1/20 0.55
ALOX15 P16050 1/20 0.55
HSD17B10 Q99714 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.55
QDPR P09417 1/20 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
SCHEMBL1078756 1.00 KDM4E (0.55) KDM4ELMNAPOLBHTR1AALOX15
SCHEMBL29387382 1.00 KDM4E (0.55) KDM4ELMNAPOLBHTR1AALOX15
SCHEMBL4159466 0.81 KDM4E (0.54) KDM4ELMNAPOLBHTR1AALOX15
Hydrochloric Acid SCHEMBL1148906 0.79 QDPR (0.65) KDM4ELMNAPOLBHTR1AALOX15
SCHEMBL13999795 0.79 L3MBTL1 (0.40) KDM4ELMNAPOLBHTR1AALOX15
SCHEMBL7255363 0.78 HTR6 (0.58) KDM4ELMNAPOLBHTR1AALOX15
SCHEMBL5547709 0.78 QDPR (0.54) KDM4ELMNAPOLBHTR1AALOX15
SCHEMBL9536817 0.78 DRD2 (0.48) KDM4ELMNAHTR1AALOX15DRD2
SCHEMBL10576624 0.78 DRD2 (0.48) KDM4ELMNAHTR1AALOX15L3MBTL1
SCHEMBL11194461 0.78 HTR6 (0.54) KDM4ELMNAPOLBHTR1AALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250032557-A1 Novel Strain Having Antagonism Against Proteus Mirabilis and Excellent Effect on Neurodegenerative Disease, and use Thereof METACEN THERAPEUTICS CO., LTD (KR) 2025-01-30 US disclosed
EP-4420667-A1 NOVEL STRAIN HAVING ANTAGONISM AGAINST PROTEUS MIRABILIS AND EXCELLENT EFFECT ON NEURODEGENERATIVE DISEASE, AND USE THEREOF Metacen Therapeutics Co., Ltd (KR) 2024-08-28 EP disclosed
WO-2023068819-A1 NOVEL STRAIN HAVING ANTAGONISM AGAINST PROTEUS MIRABILIS AND EXCELLENT EFFECT ON NEURODEGENERATIVE DISEASE, AND USE THEREOF 주식회사 메타센테라퓨틱스 2023-04-27 WO disclosed
US-10322209-B2 Polyurethanes for osteoimplants WARSAW ORTHOPEDIC, INC. (US) 2019-06-18 US disclosed
US-20180250442-A1 POLYURETHANES FOR OSTEOIMPLANTS WARSAW ORTHOPEDIC INC (US) 2018-09-06 US disclosed
EP-1434608-B1 IMPROVED BONE GRAFT WARSAW ORTHOPEDIC INC (US) 2018-08-22 EP disclosed
US-9993579-B2 Polyurethanes for osteoimplants WARSAW ORTHOPEDIC, INC. (US) 2018-06-12 US disclosed
US-20170304496-A1 POLYURETHANES FOR OSTEOIMPLANTS WARSAW ORTHOPEDIC INC (US) 2017-10-26 US disclosed
US-9789223-B2 Polyurethanes for osteoimplants WARSAW ORTHOPEDIC, INC. (US) 2017-10-17 US disclosed
US-20170240698-A1 Biodegradable Stealth Polymeric Particles Fabricated Using The Macromonomer Approach By Free Radical Dispersion Polymerization HOWARD UNIVERSITY (US) 2017-08-24 US disclosed
WO-1998016209-A9 BIOCERAMIC COMPOSITIONS 1998-08-13 WO disclosed
WO-1998016209-A2 BIOCERAMIC COMPOSITIONS ETEX CORPORATION (US) 1998-04-23 WO disclosed
EP-0832151-A2 RESPONSIVE POLYMER NETWORKS AND METHODS OF THEIR USE Gel Sciences, Inc. (US) 1998-04-01 EP disclosed
US-5674521-A DRUG DELIVERY SYSTEM COMPRISING POLYMER GEL NETWORK INCLUDING BIOLOGICALLY ACTIVE SOLUTE, SALT, LOADING POLYMER; REDUCED LOSS OF ACTIVITY UNIVERSITY OF CINCINNATI (US) 1997-10-07 US disclosed
US-5603955-A GEL NETWORK; PROTECTIVE POLYMER; PROTECTANT SALT UNIVERSITY OF CINCINNATI (US) 1997-02-18 US disclosed
WO-1997000275-A2 RESPONSIVE POLYMER NETWORKS AND METHODS OF THEIR USE GEL SCIENCES, INC. (US) 1997-01-03 WO disclosed
WO-1996002239-A2 ENHANCED LOADING OF SOLUTES INTO POLYMER GELS AND METHODS OF USE UNIVERSITY OF CINCINNATI (US) 1996-02-01 WO disclosed
EP-0584220-A1 ENGINEERING THE LOCAL INFLAMMATORY RESPONSE AS A MEANS OF CONTROLLED RELEASE DRUG DELIVERY ENDOCON, INC. (US) 1994-03-02 EP disclosed
WO-1993023012-A1 LIQUID-CONTAINING DRUG DELIVERY SYSTEM ENDOCON, INC. (US) 1993-11-25 WO disclosed
WO-1992020325-A1 ENGINEERING THE LOCAL INFLAMMATORY RESPONSE AS A MEANS OF CONTROLLED RELEASE DRUG DELIVERY ENDOCON, INC. (US) 1992-11-26 WO 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-20170240698-A1 Biodegradable Stealth Polymeric Particles Fabricated Using The Macromonomer Approach By Free Radical Dispersion Polymerization LDHA, LDHB, ALDH2 HTR1A 2440/4885SLC6A4 3047/4885HTR6 2848/4885

“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.