Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1936573

Cc1cnc(C)c(C)c1.Cl

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
CCR5 known ✓ P51681 3/20 0.42
HDAC6 known ✓ Q9UBN7 1/20 0.36
ADRA2A known ✓ P08913 1/20 0.34
ADRA2B known ✓ P18089 1/20 0.34
ADRA2C known ✓ P18825 1/20 0.34
CHRNB4 known ✓ P30926 4/20 0.33
CHRNA3 known ✓ P32297 4/20 0.33
NOS3 P29474 3/20 0.54
NOS2 P35228 3/20 0.54
NOS1 P29475 2/20 0.54
CCR1 P32246 3/20 0.42
CCR8 P51685 3/20 0.42
CYP2A6 P11509 2/20 0.41
CYP1A2 P05177 1/20 0.38
CHRNB2 P17787 4/20 0.33
CHRNA4 P43681 4/20 0.33
KDM4E B2RXH2 1/20 0.33
PSMD14 O00487 1/20 0.33
COPS5 Q92905 1/20 0.33
CNR2 P34972 1/20 0.33

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
SCHEMBL7487 0.97
SCHEMBL29382337 0.97
SCHEMBL9784696 0.97 NOS3 (0.56) NOS3NOS2NOS1CCR1CCR5
Fluoride SCHEMBL3185683 0.94 NOS3 (0.54) NOS3NOS2NOS1CCR1CCR5
SCHEMBL29735919 0.94 NOS3 (0.54) NOS3NOS2NOS1CCR1CCR5
Hydrogen Sulfide SCHEMBL5051770 0.94 NOS3 (0.54) NOS3NOS2NOS1CCR1CCR5
Iodide SCHEMBL11070567 0.94 NOS3 (0.54) NOS3NOS2NOS1CCR1CCR5
Bromide SCHEMBL10623431 0.94 NOS3 (0.54) NOS3NOS2NOS1CCR1CCR5
Acetonitrile SCHEMBL27689078 0.85 NOS3 (0.46) NOS3NOS2NOS1CCR1CCR5
Acetic Acid SCHEMBL11227068 0.84 NOS3 (0.45) NOS3NOS2NOS1CCR1CCR5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7189876-B2 Methods for preparing sertraline hydrochloride polymorphs RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. (IT) 2007-03-13 US claimed
EP-1648854-A1 METHODS FOR PREPARING SERTRALINE HYDROCHLORIDE POLYMORPHS RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.p.a. (IT) 2006-04-26 EP claimed
US-20050032907-A1 Methods for preparing sertraline hydrochloride polymorphs RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. (IT) 2005-02-10 US claimed
WO-2005012225-A1 METHODS FOR PREPARING SERTRALINE HYDROCHLORIDE POLYMORPHS RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. (IT) 2005-02-10 WO claimed
EP-1135382-A1 METHOD OF PRODUCING PAROXETINE HYDROCHLORIDE SMITHKLINE BEECHAM PLC (GB) 2001-09-26 EP claimed
WO-2000032593-A1 METHOD OF PRODUCING PAROXETINE HYDROCHLORIDE SMITHKLINE BEECHAM PLC (GB) 2000-06-08 WO claimed
US-5629134-A SOLVENT, ALKALI SOLUBLE RESIN, ACID GENERATOR, PYRIDINE SALT SHIN-ETSU CHEMICAL CO., LTD. (JP) 1997-05-13 US claimed
EP-0058591-B1 EPIMERISATION OF TRANS CHRYSANTHEMIC ACIDS AND INTERMEDIATES OBTAINED THEREFROM ROUSSEL-UCLAF (FR) 1984-10-03 EP claimed
US-4447637-A Epimerization of trans chrysanthemates ROUSSEL UCLAF (FR) 1984-05-08 US claimed
CN-120118077-A Compound and application thereof 润尔眼科药物(广州)有限公司 2025-06-10 CN disclosed
CN-119371426-A Ion channel modulators 普拉克西斯精密药物股份有限公司 2025-01-28 CN disclosed
CN-119350320-A Ion channel modulators 普拉克西斯精密药物股份有限公司 2025-01-24 CN disclosed
CN-118362466-A Hematology systems and methods 艾瑞思国际股份有限公司 2024-07-19 CN disclosed
CN-113484200-B Hematology systems and methods 艾瑞思国际股份有限公司 2024-04-26 CN disclosed
EP-0097805-A2 Nucleoside phosphite compounds UNIVERSITY PATENTS, INC. (US) 1984-01-11 EP disclosed
EP-0035719-A2 Process for producing modified inorganic polymers, their use in producing polynucleotides, and a reagent useful in these processes UNIVERSITY PATENTS, INC. (US) 1981-09-16 EP disclosed
US-4212763-A Bis-triazinylaminostilbene compounds and their use as fluorescent brightening agents CIBA-GEIGY CORPORATION (US) 1980-07-15 US disclosed
US-4110442-A CARDIOVASCULAR DISORDERS J. URIACH & CIA S.A. (ES) 1978-08-29 US disclosed
US-4096252-A THERAPY AND PROPHYLAXIS J. URIACH & CIA S.A. (ES) 1978-06-20 US disclosed
US-3979369-A DIENE POLYMER MONSANTO COMPANY (US) 1976-09-07 US 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-20050032907-A1 Methods for preparing sertraline hydrochloride polymorphs HTR1A, HTR3A, HTR5A CCR5 238/4885HDAC6 1580/4885ADRA2A 125/4885

“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.