Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3387556

CCCCCCCCc1ccccc1C(N)(CCCCCCCC)CCCCCCCC.Cl

nearest known ligand 0.47

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
S1PR1 known ✓ P21453 2/20 0.42
S1PR4 known ✓ O95977 1/20 0.40
S1PR3 known ✓ Q99500 1/20 0.40
S1PR5 known ✓ Q9H228 1/20 0.40
KCNH2 known ✓ Q12809 1/20 0.39
PPARG known ✓ P37231 1/20 0.38
LIPG Q9Y5X9 1/20 0.47
NR1H2 P55055 1/20 0.40
NR1H3 Q13133 1/20 0.40
CYSLTR2 Q9NS75 2/20 0.40
CYSLTR1 Q9Y271 2/20 0.40
TNNC1 P63316 5/20 0.40
SGPL1 O95470 1/20 0.40
GPR183 P32249 1/20 0.40
CERS2 Q96G23 1/20 0.40
BID P55957 3/20 0.38
MCL1 Q07820 3/20 0.38
BCL2L1 Q07817 2/20 0.38
BAK1 Q16611 2/20 0.38
KAT8 Q9H7Z6 2/20 0.38

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 SCHEMBL2059992 1.00 LIPG (0.47) LIPGS1PR1NR1H2NR1H3CYSLTR2
Hydrochloric Acid SCHEMBL29286909 1.00 LIPG (0.47) LIPGS1PR1NR1H2NR1H3CYSLTR2
Hydrochloric Acid SCHEMBL8591558 1.00 LIPG (0.47) LIPGS1PR1NR1H2NR1H3CYSLTR2
Hydrochloric Acid SCHEMBL15811749 1.00 LIPG (0.47) LIPGS1PR1NR1H2NR1H3CYSLTR2
SCHEMBL8592575 0.98 LIPG (0.49) LIPGS1PR1NR1H2NR1H3CYSLTR2
Hydrochloric Acid SCHEMBL28845901 0.98 LIPG (0.45) LIPGS1PR1NR1H2NR1H3CYSLTR2
SCHEMBL1537240 0.98 LIPG (0.49) LIPGS1PR1NR1H2NR1H3CYSLTR2
SCHEMBL2530765 0.98 LIPG (0.49) LIPGS1PR1NR1H2NR1H3CYSLTR2
Bromide SCHEMBL20163268 0.97 LIPG (0.47) LIPGS1PR1NR1H2NR1H3CYSLTR2
Bromide SCHEMBL11614736 0.97 LIPG (0.47) LIPGS1PR1NR1H2NR1H3CYSLTR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115894291-A Preparation method of alpha-cyhalothrin 江苏优嘉植物保护有限公司 2023-04-04 CN claimed
US-5658671-A ARTICLE COATED WITH COMPOSITION COMPRISING FLUOROELASTOMER, QUATERNARY AMMONIUM OR PHOSPHONIUM ACCELERATOR, POLYOL, ACID ACCEPTOR, OIL-SOLUBLE CHELATING AGENT, ORGANIC SOLVENT MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-08-19 US claimed
US-5451625-A FOR USE IN THE PREPARATION OF AUTOMOTIVE GASKETS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1995-09-19 US claimed
EP-0574319-A1 Fluoroelastomer coating composition MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1993-12-15 EP claimed
US-11988809-B2 Laminate, antireflection product, and manufacturing method thereof FUJIFILM CORPORATION (JP) 2024-05-21 US disclosed
US-20240085784-A1 ORGANIC EL DISPLAY DEVICE TOYO INK SC HOLDINGS CO., LTD. (JP) 2024-03-14 US disclosed
EP-4166712-A1 METHOD FOR PRODUCING COAGULATED MATERIAL DIC Corporation (JP) 2023-04-19 EP disclosed
CN-115894291-A Preparation method of alpha-cyhalothrin 江苏优嘉植物保护有限公司 2023-04-04 CN disclosed
US-11567238-B2 Laminate, antireflection product having three-dimensional curved surface, and method of manufacturing antireflection product FUJIFILM CORPORATION (JP) 2023-01-31 US disclosed
WO-2022224779-A1 ORGANIC EL DISPLAY DEVICE 東洋インキSCホールディングス株式会社 2022-10-27 WO disclosed
CN-109564384-B Photosensitive coloring composition and color filter 东洋油墨SC控股株式会社 2022-09-20 CN disclosed
CN-111825559-B Quaternary ammonium salt ionic liquid, synthesis method and application thereof as metal corrosion inhibitor 河南大学 2022-07-08 CN disclosed
US-5658671-A ARTICLE COATED WITH COMPOSITION COMPRISING FLUOROELASTOMER, QUATERNARY AMMONIUM OR PHOSPHONIUM ACCELERATOR, POLYOL, ACID ACCEPTOR, OIL-SOLUBLE CHELATING AGENT, ORGANIC SOLVENT MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-08-19 US disclosed
EP-0670868-B1 FLUORORUBBER COATING COMPOSITION MINNESOTA MINING & MFG (US) 1997-01-22 EP disclosed
US-5451625-A FOR USE IN THE PREPARATION OF AUTOMOTIVE GASKETS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1995-09-19 US disclosed
EP-0670868-A1 FLUORORUBBER COATING COMPOSITION. MINNESOTA MINING & MFG (US) 1995-09-13 EP disclosed
US-5407774-A Charge control agent and positively chargeable toner for developing electrostatic images ORIENT CHEMICAL INDUSTRIES, LTD. (JP) 1995-04-18 US disclosed
WO-1994012580-A1 FLUORORUBBER COATING COMPOSITION MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1994-06-09 WO disclosed
EP-0579207-A1 Charge control agent and positively chargeable toner for developing electrostatic images ORIENT CHEMICAL INDUSTRIES, LTD. (JP) 1994-01-19 EP disclosed
EP-0574319-A1 Fluoroelastomer coating composition MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1993-12-15 EP disclosed