Hydrochloric Acid

Hydrochloric Acid

SCHEMBL11444366

Cl.O=C1c2ccccc2C(=O)c2c1cccc2S(=O)(=O)O

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
MAOA known ✓ P21397 6/20 0.47
EGFR known ✓ P00533 2/20 0.46
MAOB known ✓ P27338 1/20 0.44
ALDH1A1 P00352 7/20 0.59
SMN1; SMN2 Q16637 4/20 0.59
PGAM1 P18669 2/20 0.57
STAT3 P40763 1/20 0.51
L3MBTL1 Q9Y468 5/20 0.50
LMNA P02545 4/20 0.50
ADORA2A P29274 2/20 0.50
THRB P10828 2/20 0.50
MAPT P10636 6/20 0.47
MAPK1 P28482 5/20 0.47
MEN1 O00255 4/20 0.47
KMT2A Q03164 4/20 0.47
HSD17B10 Q99714 3/20 0.47
MCL1 Q07820 2/20 0.47
HPGD P15428 2/20 0.47
ALOX15 P16050 2/20 0.47
KDM4E B2RXH2 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
SCHEMBL29470867 0.98 ALDH1A1 (0.61) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL230644 0.98 ALDH1A1 (0.61) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL28315391 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL2958259 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL28315392 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL5068677 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL1412693 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
SCHEMBL2787086 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
Ammonia Solution, Strong SCHEMBL10413353 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1
Formaldehyde SCHEMBL18335437 0.94 ALDH1A1 (0.57) ALDH1A1SMN1; SMN2PGAM1STAT3L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106824288-A Magnetic quinone amboceptor nano-functional material and its preparation method and application 天津城建大学 2017-06-13 CN claimed
CN-104003518-B A kind of quinonyl terylene net functional material and application thereof 河北科技大学 2016-09-14 CN claimed
CN-106824288-A Magnetic quinone amboceptor nano-functional material and its preparation method and application 天津城建大学 2017-06-13 CN disclosed
CN-104003518-B A kind of quinonyl terylene net functional material and application thereof 河北科技大学 2016-09-14 CN disclosed
CN-103937283-B A kind of modified anthraquinone stain 上海汇友精密化学品有限公司 2016-07-20 CN disclosed
US-4264511-A FOR DYEING POLYESTERS AND AS CHEMICAL INTERMEDIATE FOR DYESTUFF BAYER AKTIENGESELLSCHAFT (DE) 1981-04-28 US disclosed
US-4060549-A Process for preparing sulfonic acid fluorides BAYER AKTIENGESELLSCHAFT (DT) 1977-11-29 US disclosed