Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8922368

Cl.O=S(=O)(O)c1ccc(F)cc1F

nearest known ligand 0.45

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
KCNH2 known ✓ Q12809 1/20 0.39
GRIN2D known ✓ O15399 1/20 0.38
GRIN3B known ✓ O60391 1/20 0.38
GRIN1 known ✓ Q05586 1/20 0.38
GRIN2A known ✓ Q12879 1/20 0.38
GRIN2B known ✓ Q13224 1/20 0.38
GRIN2C known ✓ Q14957 1/20 0.38
GRIN3A known ✓ Q8TCU5 1/20 0.38
AKR1B1 P15121 1/20 0.45
CES2 O00748 2/20 0.43
CES1 P23141 2/20 0.43
POLB P06746 1/20 0.41
CCR2 P41597 3/20 0.41
TET2 Q6N021 1/20 0.40
PPME1 Q9Y570 1/20 0.39
ALDH1A1 P00352 2/20 0.38
CA3 P07451 1/20 0.38
CA6 P23280 1/20 0.38
CA5A P35218 1/20 0.38
CA9 Q16790 1/20 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
SCHEMBL795339 0.98 AKR1B1 (0.46) AKR1B1CES2CES1POLBCCR2
SCHEMBL16341240 0.96 AKR1B1 (0.45) AKR1B1CES2CES1POLBCCR2
SCHEMBL6115457 0.96 AKR1B1 (0.45) AKR1B1CES2CES1POLBCCR2
SCHEMBL16341205 0.96 AKR1B1 (0.45) AKR1B1CES2CES1POLBCCR2
Iodobenzene SCHEMBL28113125 0.84 TET2 (0.43) AKR1B1TET2KCNH2PPME1ALDH1A1
Hydrochloric Acid SCHEMBL28046977 0.83 PKM (0.46) CES2CES1POLBTET2CA3
SCHEMBL10590409 0.82 PARP1 (0.41) AKR1B1CES2CES1TET2CA3
SCHEMBL19519153 0.81 AKR1B1 (0.45) AKR1B1CES2CES1POLBCCR2
SCHEMBL3195282 0.80 PKM (0.47) CES2CES1POLBTET2CA3
SCHEMBL778076 0.79 AKR1B1 (0.58) AKR1B1CES2CES1POLBCCR2

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-108503640-B Sparteine derivative and preparation method thereof and the utilization in pesticide 广西田园生化股份有限公司 2019-11-12 CN disclosed
CN-106795149-B Double cyclosubstituted benzenesulfonamide derivatives, its preparation method and purposes pharmaceutically 上海海雁医药科技有限公司 2019-09-24 CN disclosed
CN-106220618-B Sulfur derivatives as chemokine receptor modulators 阿勒根公司 2019-04-26 CN disclosed
CN-108503640-A Sparteine derivative and preparation method thereof and the utilization in pesticide 广西田园生化股份有限公司 2018-09-07 CN disclosed
CN-104822672-B The purposes of therapeutic compound and composition as well as PKM2 conditioning agents 安吉奥斯医药品有限公司 2018-08-28 CN disclosed
CN-107163169-A One class cumarin and carbazole type oxime ester compound and its preparation method and application 同济大学 2017-09-15 CN disclosed
CN-103965199-B A kind of heteroaromatic compounds, the medical composition and its use comprising it 广东东阳光药业有限公司 2017-07-07 CN disclosed
US-5625067-A Cyclopentane ether derivatives, processes for their production, and their pharmaceutical use SCHERING AKTIENGESELLSCHAFT (DE) 1997-04-29 US disclosed