Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8045536

Cl.Nc1ccc(O)c(Cl)c1Cl

nearest known ligand 0.52

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
▸ CA2 known ✓ P00918 2/20 0.41
▸ HDAC3 known ✓ O15379 1/20 0.41
▸ GAA known ✓ P10253 2/20 0.35
▸ ESR2 known ✓ Q92731 1/20 0.35
▸ HSP90AA1 known ✓ P07900 1/20 0.35
▸ CYP3A4 P08684 5/20 0.52
▸ MAPK1 P28482 3/20 0.52
▸ ALDH1A1 P00352 7/20 0.46
▸ ALOX15 P16050 5/20 0.46
▸ HSD17B10 Q99714 4/20 0.46
▸ SMN1; SMN2 Q16637 3/20 0.46
▸ HPGD P15428 2/20 0.46
▸ ALOX12 P18054 1/20 0.46
▸ CA1 P00915 2/20 0.41
▸ IDO1 P14902 1/20 0.41
▸ EP300 Q09472 1/20 0.41
▸ KAT2B Q92831 1/20 0.41
▸ KAT8 Q9H7Z6 1/20 0.41
▸ NCOR2 Q9Y618 1/20 0.41
▸ CSNK2A2 P19784 1/20 0.39

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 SCHEMBL29972242 1.00 CYP3A4 (0.52) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL1456970 0.97 CYP3A4 (0.55) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
Sulfuric Acid SCHEMBL9103041 0.86 ALDH1A1 (0.48) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
Sulfuric Acid SCHEMBL9103050 0.81 ALDH1A1 (0.44) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL7605518 0.81 CA1 (0.73) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL526351 0.80 ALDH1A1 (0.50) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL31392414 0.80 CYP3A4 (0.75) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL7743436 0.80 CYP3A4 (0.75) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL68064 0.80 CYP3A4 (0.75) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10
SCHEMBL94373 0.79 ALOX15 (0.46) CYP3A4MAPK1ALDH1A1ALOX15HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115304505-B Process for synthesizing amide by carbonylation of olefine 西北大学 2023-06-27 — — CN disclosed
CN-115304505-A Method for synthesizing amide by olefin carbonylation 西北大学 2022-11-08 — — CN disclosed
EP-0720980-B1 Process for the preparation of 4-hydroxyanilides of alkylcarboxylic acid BAYER AG (DE) 2000-04-26 — — EP disclosed
US-5621141-A Process for the preparation of alkylcarboxylic acid 4-hydroxyanilides BAYER AKTIENGESELLSCHAFT (DE) 1997-04-15 — — US disclosed
EP-0720980-A1 Process for the preparation of 4-hydroxyanilides of alkylcarboxylic acid BAYER AG (DE) 1996-07-10 — — EP disclosed
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