Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8522902

Cl.O=C(O)c1ccc2c(C(=O)O)cccc2c1

nearest known ligand 0.96

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
GRIN2D known ✓ O15399 2/20 0.47
GRIN2A known ✓ Q12879 2/20 0.47
GRIN2C known ✓ Q14957 2/20 0.47
GRIN2B known ✓ Q13224 1/20 0.47
CA2 known ✓ P00918 1/20 0.47
PTPN1 P18031 1/20 0.96
NR4A1 P22736 1/20 0.60
NR4A2 P43354 1/20 0.60
NR4A3 Q92570 1/20 0.60
PLA2G2D Q9UNK4 1/20 0.51
CDC25B P30305 2/20 0.49
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
PTPN11 Q06124 1/20 0.48
CA12 O43570 1/20 0.47
CA1 P00915 1/20 0.47
CA6 P23280 1/20 0.47
CA9 Q16790 1/20 0.47
HSD17B10 Q99714 2/20 0.47
ACE2 Q9BYF1 1/20 0.46

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 SCHEMBL11707739 1.00 PTPN1 (0.96) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL29404396 0.98 PTPN1 (1.00) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL70015 0.98 PTPN1 (1.00) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL27906674 0.96 PTPN1 (0.96) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL8898819 0.95 PTPN1 (0.93) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL3060737 0.95 PTPN1 (0.93) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL7746811 0.91 PTPN1 (0.87) PTPN1NR4A1NR4A2NR4A3PLA2G2D
SCHEMBL7623416 0.91 PTPN1 (0.87) PTPN1NR4A1NR4A2NR4A3PLA2G2D
Ethylene Glycol SCHEMBL27888858 0.91 PTPN1 (0.87) PTPN1NR4A1NR4A2NR4A3PLA2G2D
Paraben SCHEMBL5690434 0.90 PTPN1 (0.84) PTPN1NR4A1NR4A2NR4A3PLA2G2D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0552499-B1 Wholly aromatic polyamide resin composition having enhanced light resistance TEIJIN LTD (JP) 1999-03-31 EP disclosed
EP-0643039-B1 Ultraviolet ray-absorbing aromatic compound and polymeric composition containing the same TEIJIN LTD (JP) 1997-07-30 EP disclosed
US-5532412-A HEAT RESISTANT, POLYAMIDES TEIJIN LIMITED (JP) 1996-07-02 US disclosed
EP-0643039-A1 Ultraviolet ray-absorbing aromatic compound and polymeric composition containing the same TEIJIN LIMITED (JP) 1995-03-15 EP disclosed
US-5312851-A Benzene and naphthalene containing polyamides with terminal imide groups TEIJIN LIMITED (JP) 1994-05-17 US disclosed
EP-0552499-A2 Wholly aromatic polyamide resin composition having enhanced light resistance TEIJIN LIMITED (JP) 1993-07-28 EP disclosed
EP-0005858-B1 PREPARATION OF POLYARYLATES UNION CARBIDE CORPORATION (US) 1983-05-11 EP disclosed
US-4229565-A BY FORMATION OF THE ACYL CHLORIDE THEN POLYMERIZING TO FORM HIGH MOLECULAR WEIGHT, HEAT RESISTANT POLYESTERS UNION CARBIDE CORPORATION (US) 1980-10-21 US disclosed
EP-0005858-A1 Preparation of polyarylates UNION CARBIDE CORPORATION (US) 1979-12-12 EP disclosed