Hydrochloric Acid

Hydrochloric Acid

SCHEMBL10352018

CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Br)CCN1.Cl

nearest known ligand 0.76

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
KCNH2 known ✓ Q12809 7/20 0.76
OPRM1 known ✓ P35372 2/20 0.76
PRKD3 known ✓ O94806 1/20 0.76
CHRM2 known ✓ P08172 1/20 0.56
CHRM1 known ✓ P11229 1/20 0.56
OPRD1 known ✓ P41143 1/20 0.56
HRH3 known ✓ Q9Y5N1 1/20 0.54
TOP2A known ✓ P11388 1/20 0.51
TOP2B known ✓ Q02880 1/20 0.51
CACNA1F known ✓ O60840 1/20 0.49
CACNA1D known ✓ Q01668 1/20 0.49
CACNA1S known ✓ Q13698 1/20 0.49
CACNA1C known ✓ Q13936 1/20 0.49
ALDH1A1 P00352 8/20 0.76
KDM4E B2RXH2 8/20 0.76
HPGD P15428 7/20 0.76
HSD17B10 Q99714 5/20 0.76
POLB P06746 4/20 0.76
TDP1 Q9NUW8 2/20 0.76
ALOX15 P16050 1/20 0.76

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
SCHEMBL29593740 0.91 ALDH1A1 (0.81) ALDH1A1KDM4EHPGDKCNH2HSD17B10
SCHEMBL6783172 0.91 ALDH1A1 (0.81) ALDH1A1KDM4EHPGDKCNH2HSD17B10
Hydrochloric Acid SCHEMBL10914782 0.89 ALDH1A1 (0.76) ALDH1A1KDM4EHPGDKCNH2HSD17B10
SCHEMBL3957125 0.89 ALDH1A1 (0.79) ALDH1A1KDM4EHPGDKCNH2HSD17B10
SCHEMBL9792010 0.89 KCNH2 (0.79) ALDH1A1KDM4EHPGDKCNH2HSD17B10
SCHEMBL8433684 0.88 ALDH1A1 (0.77) ALDH1A1KDM4EHPGDKCNH2HSD17B10
Gatifloxacin SCHEMBL3339392 0.88 KDM4E (0.98) ALDH1A1KDM4EHPGDKCNH2HSD17B10
(S)-Gatifloxacin SCHEMBL3339394 0.88 KDM4E (0.98) ALDH1A1KDM4EHPGDKCNH2HSD17B10
SCHEMBL9485535 0.87 ALDH1A1 (0.76) ALDH1A1KDM4EHPGDKCNH2HSD17B10
SCHEMBL10351473 0.87 TOP2A (0.64) ALDH1A1KDM4EHPGDKCNH2HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4826982-A BACTERICIDES KYORIN PHARMACEUTICAL CO., LTD. (JP) 1989-05-02 US claimed
EP-0216245-B1 QUINOLONECARBOXYLIC ACID DERIVATIVES AND PROCESS FOR THEIR PREPARATION KYORIN PHARMACEUTICAL CO., LTD. (JP) 1990-07-25 EP disclosed
US-4826982-A BACTERICIDES KYORIN PHARMACEUTICAL CO., LTD. (JP) 1989-05-02 US disclosed
EP-0216245-A1 Quinolonecarboxylic acid derivatives and process for their preparation KYORIN PHARMACEUTICAL CO., LTD. (JP) 1987-04-01 EP disclosed