Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6137451

Cl.O=C(O)c1sc(C(F)(F)F)nc1C(F)(F)F

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 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.39
ALDH1A1 P00352 3/20 0.37
HPGD P15428 1/20 0.36
TSHR P16473 1/20 0.36
POLB P06746 2/20 0.36
GPR35 Q9HC97 1/20 0.35
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.33
DAO P14920 1/20 0.32
CDC7 O00311 1/20 0.30
DBF4 Q9UBU7 1/20 0.30
NOTUM Q6P988 1/20 0.30
GRIA2 P42262 1/20 0.30
GRIA4 P48058 1/20 0.30
CYP2C9 P11712 1/20 0.30
CYP2C19 P33261 1/20 0.30

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
SCHEMBL6137459 0.98 MAPT (0.40) MAPTALDH1A1HPGDTSHRPOLB
SCHEMBL5528567 0.85 MAPT (0.40) MAPTALDH1A1HPGDTSHRPOLB
Hydrochloric Acid SCHEMBL10820945 0.81 ALDH1A1 (0.53) MAPTALDH1A1HPGDTSHRPOLB
SCHEMBL6137447 0.81 MAPT (0.37) MAPTALDH1A1POLBMEN1KMT2A
Hydrochloric Acid SCHEMBL9644334 0.79 ALDH1A1 (0.52) ALDH1A1HPGDTSHRPOLBKMT2A
SCHEMBL9643819 0.78 MAPT (0.40) MAPTALDH1A1HPGDTSHRPOLB
SCHEMBL873879 0.78 GPR35 (0.43) MAPTALDH1A1HPGDTSHRPOLB
SCHEMBL1778181 0.78 ALDH1A1 (0.55) MAPTALDH1A1HPGDTSHRPOLB
SCHEMBL16346305 0.77 GPR35 (0.42) ALDH1A1HPGDTSHRPOLBGPR35
SCHEMBL9643792 0.77 ALDH1A1 (0.53) ALDH1A1HPGDTSHRPOLBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1110956-B1 The use of 5-carboxanilido-2,4-bis-trifluoromethylthiazoles to control rice blast DOW AGROSCIENCES LLC (US) 2005-02-23 EP disclosed
EP-1112688-B1 A method to control termites DOW AGROSCIENCES LLC (US) 2004-09-22 EP disclosed
US-6423730-B1 FLUORINATED TRIAZOLE RING CONTAINING COMPOUND DOW AGROSCIENCES LLC 2002-07-23 US disclosed
US-6372769-B1 APPLYING FUNGICIDES TO RICE DOW AGROSCIENCES LLC 2002-04-16 US disclosed
EP-1112688-A1 A method to control termites ROHM AND HAAS COMPANY (US) 2001-07-04 EP disclosed
EP-1110956-A1 5-carboxanilido-2,4-bis-trifluoromethylthiazoles and their use to control rice blast ROHM AND HAAS COMPANY (US) 2001-06-27 EP disclosed
EP-1110454-A2 5-Carboxanilido-haloalkylthiazoles as antimicrobial and marine antifouling agents ROHM AND HAAS COMPANY (US) 2001-06-27 EP disclosed
EP-1108714-A1 Microbicidal salts of 5-carboxanilido-haloalkylthiazoles ROHM AND HAAS COMPANY (US) 2001-06-20 EP disclosed