Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9344276

CCCCCCCCCCC(Cc1ccccc1)C(P)(CC)CC.Cl

nearest known ligand 0.49

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 15)

geneUniProtsupporting neighboursconfidence
KCNH2 known ✓ Q12809 1/20 0.39
SIGMAR1 known ✓ Q99720 1/20 0.38
MMP1 known ✓ P03956 4/20 0.38
HTR2A known ✓ P28223 1/20 0.37
CSNK1E P49674 1/20 0.49
CNR2 P34972 1/20 0.38
MMP2 P08253 9/20 0.38
MMP3 P08254 4/20 0.38
DNM1 Q05193 1/20 0.37
MEN1 O00255 1/20 0.36
TP53 P04637 1/20 0.36
MAPK1 P28482 1/20 0.36
KMT2A Q03164 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
EPHX2 P34913 1/20 0.36

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
SCHEMBL9518672 0.98 CSNK1E (0.50) CSNK1EKCNH2SIGMAR1CNR2MMP2
Water SCHEMBL9246740 0.97 CSNK1E (0.49) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5091962 0.90 CSNK1E (0.51) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5088606 0.90 CSNK1E (0.51) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5092844 0.90 CSNK1E (0.51) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5086841 0.90 CSNK1E (0.51) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL9342636 0.90 CSNK1E (0.48) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5091828 0.90 CSNK1E (0.51) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5093032 0.90 CSNK1E (0.51) CSNK1EKCNH2SIGMAR1CNR2MMP2
Hydrochloric Acid SCHEMBL5088207 0.88 CSNK1E (0.49) CSNK1EKCNH2SIGMAR1CNR2MMP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0499743-B1 Two step process for sweetening a sour hydrocarbon fraction UOP INC (US) 1994-07-20 EP disclosed
US-5273646-A Adding aqueous ammonium hydroxide, metal chelate and an onium compound to the hydrocarbon fraction containing an oxidizer and base UOP (US) 1993-12-28 US disclosed
EP-0394571-B1 USE OF A NOVEL CATALYTIC COMPOSITE FOR SWEETENING OF SOUR PETROLEUM DISTILLATE UOP (US) 1993-09-01 EP disclosed
US-5204306-A Oxidizing mercaptans to disulfides with metal chelate catalyst and an onium component UOP (US) 1993-04-20 US disclosed
US-5180484-A Oxidation in presence of ammonium hydroxide, metal chelate and onium compound UOP (US) 1993-01-19 US disclosed
EP-0499743-A1 Two step process for sweetening a sour hydrocarbon fraction UOP (US) 1992-08-26 EP disclosed
US-5093296-A Caustic free liquid/liquid process for sweetening a sour hydrocarbon fraction UOP (US) 1992-03-03 US disclosed
US-5064525-A Catalysis; hydrogenation UOP (US) 1991-11-12 US disclosed
EP-0394571-A1 Use of a novel catalytic composite for sweetening of sour petroleum distillate UOP (US) 1990-10-31 EP disclosed
US-4908122-A Contacting hydrocarbon in the presence of an oxidizing agent with a catalytic composite to oxidize mercaptans to disulfides UOP (US) 1990-03-13 US disclosed
US-4897180-A Catalytic composite and process for mercaptan sweetening UOP (US) 1990-01-30 US disclosed
US-4824818-A OXIDATION CATALYST CONTAINING METAL CHELATE AND ONIUM COMPOUND UOP INC. (US) 1989-04-25 US disclosed