Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8986262

C=CCOc1ccc(-c2ccc(C(=O)O)cc2)cc1.Cl

nearest known ligand 0.59

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
CHRNB4 known ✓ P30926 1/20 0.48
CHRNA3 known ✓ P32297 1/20 0.48
CA2 known ✓ P00918 1/20 0.46
ALDH1A1 P00352 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
RARB P10826 5/20 0.53
HTT P42858 1/20 0.52
FFAR1 O14842 1/20 0.51
NPC1 O15118 3/20 0.50
MAPT P10636 2/20 0.50
RAB9A P51151 2/20 0.50
SRD5A2 P31213 1/20 0.50
PKM P14618 1/20 0.50
POLB P06746 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
HSD17B10 Q99714 1/20 0.49
CHRNB2 P17787 1/20 0.48
CHRNA4 P43681 1/20 0.48
NR4A1 P22736 1/20 0.47
NR4A2 P43354 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
SCHEMBL5840304 0.98 ALDH1A1 (0.61) ALDH1A1L3MBTL1RARBHTTFFAR1
Hydrochloric Acid SCHEMBL711176 0.95 ALDH1A1 (0.65) ALDH1A1L3MBTL1HTTFFAR1NPC1
SCHEMBL1489146 0.93 ALDH1A1 (0.67) ALDH1A1L3MBTL1HTTFFAR1NPC1
Biphenyl SCHEMBL5095997 0.92 ALDH1A1 (0.58) ALDH1A1L3MBTL1RARBHTTFFAR1
Benzene SCHEMBL28158854 0.91 ALDH1A1 (0.65) ALDH1A1L3MBTL1HTTFFAR1NPC1
Benzoic Acid SCHEMBL9750866 0.90 FFAR1 (0.55) ALDH1A1L3MBTL1RARBHTTFFAR1
Hydroquinone SCHEMBL7626940 0.87 ALDH1A1 (0.59) ALDH1A1L3MBTL1HTTFFAR1NPC1
Hydroquinone SCHEMBL8024416 0.87 ALDH1A1 (0.59) ALDH1A1L3MBTL1HTTFFAR1NPC1
SCHEMBL7357344 0.86 NR1H4 (0.63) ALDH1A1L3MBTL1RARBHTTFFAR1
Hydrochloric Acid SCHEMBL8861914 0.86 ALDH1A1 (0.55) ALDH1A1L3MBTL1HTTFFAR1NPC1

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-3123759-A None JP disclosed
JP-5186401-A None JP disclosed
JP-6192198-A None JP disclosed
EP-0571277-B1 Antiferroelectric liquid crystal compound SHOWA SHELL SEKIYU (JP) 1996-06-26 EP disclosed
EP-0422996-B1 Liquid crystal compound SHOWA SHELL SEKIYU (JP) 1995-04-12 EP disclosed
EP-0466573-B1 Liquid crystal compositions SHOWA SHELL SEKIYU (JP) 1995-02-15 EP disclosed
US-5364561-A Diluent; optically tristable; electrooptics SHOWA SHELL SEKIYU KABUSHIKI KAISHA (JP) 1994-11-15 US disclosed
US-5328641-A Naphthalene ester derivatives with trifluoromethyl groups SHOWA SHELL SEKIYU KABUSHIKI KAISHA 1994-07-12 US disclosed
JP-H06192198-A LIQUID CRYSTAL COMPOUND SHOWA SHELL SEKIYU KK 1994-07-12 JP disclosed
US-5320776-A Antiferroelectric liquid crystal compound SHOWA SHELL SEKIYU KABUSHIKI KAISHA (JP) 1994-06-14 US disclosed
EP-0571277-A1 Antiferroelectric liquid crystal compound Showa Shell Sekiyu Kabushiki Kaisha (JP) 1993-11-24 EP disclosed
JP-H05186401-A LIQUID CRYSTAL COMPOUND AND LIQUID CRYSTAL COMPOSITION CONTAINING THE SAME SHOWA SHELL SEKIYU KK 1993-07-27 JP disclosed
US-5207947-A Trifluoroalkyl diaryl triesters; antiferroelectricity; electrooptics SHOWA SHELL SEKIYU KABUSHIKI KAISHA (JP) 1993-05-04 US disclosed
EP-0466573-A2 Liquid crystal compositions Showa Shell Sekiyu Kabushiki Kaisha (JP) 1992-01-15 EP disclosed
JP-H03123759-A LIQUID CRYSTAL COMPOUND SHOWA SHELL SEKIYU KK 1991-05-27 JP disclosed
US-4820444-A SUPERIOR FERROELECTRIC MATERIAL CHISSO CORPORATION (JP) 1989-04-11 US disclosed
EP-0115693-B1 LIQUID CRYSTALLINE COMPOUNDS AND MIXTURES THEREOF Chisso Corporation (JP) 1987-08-26 EP disclosed
US-4596667-A Phenyl ester derivatives CHISSO CORPORATION (JP) 1986-06-24 US disclosed
EP-0115693-A2 Liquid crystalline compounds and mixtures thereof Chisso Corporation (JP) 1984-08-15 EP disclosed