Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9342790

CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)OCOC(=O)C3=C(COC(C)=O)CS[C@@H]4[C@H](NC(=O)/C(=N\OC)c5csc(N)n5)C(=O)N34)=C(COC(C)=O)CS[C@H]12)c1csc(N)n1.Cl

nearest known ligand 0.85

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
▸ PPARG known ✓ P37231 1/20 0.85
▸ HTR2C known ✓ P28335 1/20 0.73
▸ PTGS1 known ✓ P23219 2/20 0.71
▸ PDE4D known ✓ Q08499 1/20 0.68
▸ ESR1 known ✓ P03372 1/20 0.63
▸ DRD2 known ✓ P14416 1/20 0.63
▸ ADRA2B known ✓ P18089 1/20 0.63
▸ HRH3 known ✓ Q9Y5N1 1/20 0.63
▸ ADRA1A known ✓ P35348 1/20 0.58
▸ MAPT P10636 5/20 0.85
▸ NR1I2 O75469 4/20 0.85
▸ ALB P02768 1/20 0.85
▸ SLC22A6 Q4U2R8 1/20 0.85
▸ SLC22A8 Q8TCC7 1/20 0.85
▸ SLC22A11 Q9NSA0 1/20 0.85
▸ TDP1 Q9NUW8 5/20 0.82
▸ APEX1 P27695 3/20 0.82
▸ HSD17B10 Q99714 3/20 0.82
▸ ALDH1A1 P00352 3/20 0.82
▸ POLB P06746 2/20 0.82

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
SCHEMBL10744602 0.95 NR1I2 (0.80) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL10744605 0.95 NR1I2 (0.80) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL9684883 0.95 NR1I2 (0.88) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL10741947 0.94 PTGS1 (0.81) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL9683679 0.94 PTGS1 (0.81) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL10741940 0.94 PTGS1 (0.81) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL9683546 0.93 NR1I2 (0.85) MAPTNR1I2ALBPPARGSLC22A6
SCHEMBL11014395 0.93 MAPT (0.75) MAPTNR1I2ALBPPARGSLC22A6
Cefotaxime SCHEMBL6017906 0.93 NR1I2 (0.98) MAPTNR1I2ALBPPARGSLC22A6
Cefotaxime SCHEMBL9342532 0.93 NR1I2 (0.98) MAPTNR1I2ALBPPARGSLC22A6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5359057-A Reacting 6-aminopenicillin derivative in the form of an acid addition salt with 2-benzothiazolyl thioester derivative to form amide of penecillin or cephalosporin derivatives; microbiocides HOFFMANN-LA ROCHE INC. (US) 1994-10-25 — — US disclosed
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