Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2066264

CCCNC(=O)/C(C)=C(/C)N.Cl

nearest known ligand 0.39

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
MMP1 known ✓ P03956 1/20 0.39
GAA known ✓ P10253 1/20 0.35
DPP4 known ✓ P27487 1/20 0.33
MMP2 P08253 1/20 0.39
MMP3 P08254 1/20 0.39
MMP9 P14780 1/20 0.39
EPHX1 P07099 2/20 0.38
PAOX Q6QHF9 1/20 0.36
MCL1 Q07820 1/20 0.36
NPC1 O15118 1/20 0.35
MAPT P10636 1/20 0.35
RAB9A P51151 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
KDM4C Q9H3R0 1/20 0.34
PLA2G4A P47712 1/20 0.34
CTSD P07339 1/20 0.33
LMNA P02545 1/20 0.33
KDM4E B2RXH2 3/20 0.33
KMT2A Q03164 2/20 0.33
TDP1 Q9NUW8 1/20 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
SCHEMBL36267 0.98 MMP1 (0.40) MMP1MMP2MMP3MMP9EPHX1
Chloromethane SCHEMBL4631102 0.94 MMP1 (0.38) MMP1MMP2MMP3MMP9EPHX1
Acetone SCHEMBL10451495 0.94 MCL1 (0.39) MMP1MMP2MMP3MMP9EPHX1
Sulfuric Acid SCHEMBL2065285 0.90 EPHX1 (0.38) MMP1MMP2MMP3MMP9EPHX1
Acrylamide SCHEMBL11143542 0.87 ALDH1A1 (0.39) MMP1MMP2MMP3MMP9EPHX1
SCHEMBL994218 0.85 EPHX1 (0.47) MMP2EPHX1PLA2G4ADPP7
SCHEMBL7129427 0.84 MMP1 (0.40) MMP1MMP2MMP3MMP9EPHX1
SCHEMBL6933418 0.84 PLA2G4A (0.32) MMP1MMP2MMP3MMP9EPHX1
SCHEMBL2066063 0.84 EPHX1 (0.34) MMP1MMP2MMP3MMP9EPHX1
SCHEMBL1067451 0.83 EPHX1 (0.52) EPHX1PLA2G4ADPP7

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 46 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2109441-B1 POLYSILOXANE BLOCK COPOLYMERS BASF SE (DE) 2016-01-27 EP claimed
US-8378038-B2 Polysiloxane block copolymers BASF SE (DE) 2013-02-19 US claimed
US-20100303750-A1 POLYSILOXANE BLOCK COPOLYMERS KOROSKENYI BALINT 2010-12-02 US claimed
EP-2109441-A2 POLYSILOXANE BLOCK COPOLYMERS Ciba Holding Inc. (CH) 2009-10-21 EP claimed
US-20080199418-A1 Polysiloxane block copolymers BASF SE (DE) 2008-08-21 US claimed
WO-2008095822-A2 POLYSILOXANE BLOCK COPOLYMERS CIBA HOLDING INC. (CH) 2008-08-14 WO claimed
EP-3116919-B1 NEW POLYELECTROLYTIC POLYMERS, PROCESS FOR THEIR PREPARATION AND USES THEREOF ITALMATCH CHEMICALS SPA (IT) 2020-08-26 EP disclosed
US-9771437-B2 Polyelectrolytic polymers, process for their preparation and uses thereof ITALMATCH CHEMICALS S.P.A. (IT) 2017-09-26 US disclosed
US-20170107310-A1 New polyelectrolytic polymers, process for their preparation and uses thereof ITALMATCH CHEMICALS S.P.A. (IT) 2017-04-20 US disclosed
EP-3116919-A1 NEW POLYELECTROLYTIC POLYMERS, PROCESS FOR THEIR PREPARATION AND USES THEREOF Italmatch Chemicals S.P.A. (IT) 2017-01-18 EP disclosed
EP-2109441-B1 POLYSILOXANE BLOCK COPOLYMERS BASF SE (DE) 2016-01-27 EP disclosed
WO-2015136438-A1 NEW POLYELECTROLYTIC POLYMERS, PROCESS FOR THEIR PREPARATION AND USES THEREOF G.R.S. CHEMICAL TECHNOLOGIES S.R.L. (IT) 2015-09-17 WO disclosed
US-8378038-B2 Polysiloxane block copolymers BASF SE (DE) 2013-02-19 US disclosed
US-20050261394-A1 Polymers for paper and paperboard coatings CIBA SPECIALTY CHEMICALS WATER TREATMENT LIMITED (GB) 2005-11-24 US disclosed
US-20050224420-A1 Enhanced recovery of useful coal, potassium chloride and borax from screen bowl centrifuge ECOLAB USA INC. 2005-10-13 US disclosed
EP-1363957-A4 CATIONIC LATEX TERPOLYMERS FOR SLUDGE DEWATERING ONDEO NALCO CO (US) 2005-06-22 EP disclosed
EP-1363957-A1 CATIONIC LATEX TERPOLYMERS FOR SLUDGE DEWATERING Ondeo Nalco Company (US) 2003-11-26 EP disclosed
US-6627719-B2 Interpolymer of a cationic monomer, a hydroxyalkyl (meth)acrylate and, optionally, a nonionic monomer ONDEO NALCO COMPANY 2003-09-30 US disclosed
US-20030060586-A1 Cationic latex terpolymers for sludge dewatering ECOLAB USA INC. 2003-03-27 US disclosed
WO-2002060967-A1 CATIONIC LATEX TERPOLYMERS FOR SLUDGE DEWATERING ONDEO NALCO COMPANY (US) 2002-08-08 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20170107310-A1 New polyelectrolytic polymers, process for their preparation and uses thereof PARG, PARN, PCBP1 MMP1 4468/4885GAA 1373/4885DPP4 4740/4885
US-20100303750-A1 POLYSILOXANE BLOCK COPOLYMERS KRT18, PUF60, SCNN1B MMP1 1659/4885GAA 3724/4885DPP4 4155/4885
US-20080199418-A1 Polysiloxane block copolymers KRT18, PUF60, SCNN1B MMP1 1659/4885GAA 3724/4885DPP4 4155/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.