Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6334189

CC(C)(c1ccc(O)cc1)c1ccc(OCc2cccc(COc3ccc(C(=N)NC(=O)O)cc3)c2)cc1.Cl

nearest known ligand 0.50

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 19)

geneUniProtsupporting neighboursconfidence
MAOB known ✓ P27338 3/20 0.46
F2 P00734 3/20 0.48
PTPRC P08575 1/20 0.48
PTPN1 P18031 1/20 0.48
MRGPRX4 Q96LA9 4/20 0.47
NR4A2 P43354 3/20 0.46
GRM5 P41594 1/20 0.44
NR1H4 Q96RI1 1/20 0.44
RXRA P19793 2/20 0.44
RXRB P28702 2/20 0.44
TP53 P04637 2/20 0.43
PKM P14618 2/20 0.43
NFKB1 P19838 2/20 0.43
NFKB2 Q00653 2/20 0.43
RELA Q04206 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
RXRG P48443 1/20 0.43
RAB9A P51151 1/20 0.43
RXFP1 Q9HBX9 1/20 0.43

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
SCHEMBL4314299 0.99 PTPRC (0.49) F2PTPRCPTPN1MRGPRX4NR4A2
Amelubant SCHEMBL29359085 0.89 GRM5 (0.45) F2PTPRCPTPN1MRGPRX4NR4A2
Amelubant SCHEMBL1891670 0.89 GRM5 (0.45) F2PTPRCPTPN1MRGPRX4NR4A2
SCHEMBL5200582 0.85 PTPRC (0.46) F2PTPRCPTPN1MRGPRX4NR4A2
Hydrochloric Acid SCHEMBL6557386 0.82 F2 (0.73) F2
SCHEMBL31506335 0.81 F2 (0.72) F2
SCHEMBL4999957 0.81 F2 (0.72) F2
Hydrochloric Acid SCHEMBL7631983 0.81 F2 (0.46) F2PTPRCPTPN1MRGPRX4NR4A2
SCHEMBL668003 0.79 PTPRC (0.46) F2PTPRCPTPN1MRGPRX4NR4A2
SCHEMBL22120093 0.79 NR4A1 (0.64) PTPRCPTPN1NR4A2MAOBSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6417382-B1 None US disclosed
US-6861547-B2 Process for preparing aryl-iminomethyl-carbamino acid esters BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-03-01 US disclosed
US-20020137963-A1 Process for preparing aryl-iminomethyl-carbamino acid esters BRANDENBURG JOERG (DE) 2002-09-26 US disclosed
US-6417382-B2 REACTING 4-((3-(PHENOXYMETHYL)PHENOXYMETHYL)BENZONITRILE WITH AN ALKALI METAL HEXAALKYLDISILAZANE AND TREATING THE RESULTING COMPOUND WITH A CARBONATE OR HALOFORMATE, FORMING A PROTIC ACID SALT, ISOLATING THE SALT AND TREATING WITH BASE BOEHRINGER INGELHEIM PHARMA KG (DE) 2002-07-09 US disclosed
US-20010009958-A1 Process for preparing aryl-iminomethyl-carbamino acid esters BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2001-07-26 US 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 (2 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-20020137963-A1 Process for preparing aryl-iminomethyl-carbamino acid esters MEP1A, CPS1, CYP51A1 MAOB 899/4885F2 1828/4885PTPRC 2831/4885
US-20010009958-A1 Process for preparing aryl-iminomethyl-carbamino acid esters MEP1A, CPS1, CYP51A1 MAOB 899/4885F2 1828/4885PTPRC 2831/4885

“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.