Hydrochloric Acid

Hydrochloric Acid

SCHEMBL11523265

Cl.O=S(=O)(O)C1CCCCC1

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
GABRA1 known ✓ P14867 1/20 0.52
GABRG2 known ✓ P18507 1/20 0.52
GABRB3 known ✓ P28472 1/20 0.52
GABRA5 known ✓ P31644 1/20 0.52
GABRA3 known ✓ P34903 1/20 0.52
GABRA2 known ✓ P47869 1/20 0.52
GABRA6 known ✓ Q16445 1/20 0.52
CA2 known ✓ P00918 2/20 0.33
TSHR P16473 3/20 0.52
CYP3A4 P08684 2/20 0.52
LMNA P02545 1/20 0.52
NFKB1 P19838 1/20 0.52
EPHX2 P34913 3/20 0.37
CA1 P00915 3/20 0.36
CA12 O43570 2/20 0.36
CA7 P43166 2/20 0.36
CA14 Q9ULX7 2/20 0.36
CES2 O00748 1/20 0.35
CES1 P23141 1/20 0.35
EPHX1 P07099 6/20 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
Hydrochloric Acid SCHEMBL28259930 1.00 TSHR (0.52) TSHRCYP3A4LMNAGABRA1GABRG2
Hydrochloric Acid SCHEMBL27291938 0.97 TSHR (0.50) TSHRCYP3A4LMNAGABRA1GABRG2
Hydrochloric Acid SCHEMBL27291937 0.97 TSHR (0.50) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL17022282 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL329394 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL2024638 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL15586623 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL3004 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL329461 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2
SCHEMBL10012314 0.97 TSHR (0.55) TSHRCYP3A4LMNAGABRA1GABRG2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-207108884-U N‑(Cyclohexyl thio)The manufacture device of phthalimide 东丽精细化工株式会社 2018-03-16 CN disclosed
CN-103370307-B Sulfonamide compounds and preparation method thereof and using method ZAFGEN CORP. (US) 2016-05-25 CN disclosed
CN-101808516-B N- (arylamino) sulfonamide derivatives and compositions, including polymorphs, as MEK inhibitors, methods of use, and methods of preparation thereof ARDEA BIOSCIENCES INC 2013-08-28 CN disclosed
CN-102458580-A Heterocyclic compounds as MEK inhibitors NOVARTIS AG 2012-05-16 CN disclosed
CN-102083312-A Benzene sulfonamide thiazole and oxazole compounds SMITHKLINE BEECHAM CORP 2011-06-01 CN disclosed
CN-101808516-A N- (arylamino) sulfonamide derivatives and compositions, including polymorphs, as MEK inhibitors, methods of use, and methods of preparation thereof ARDEA BIOSCIENCES INC 2010-08-18 CN disclosed
CN-1037568-C Phosphosulfonate herbicides ROHM & HAAS (US) 1998-03-04 CN disclosed
US-4163013-A Diphenylamine-azo-hydrocarbylsulfonylphenyl dyestuffs BAYER AKTIENGESELLSCHAFT (DE) 1979-07-31 US disclosed