Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9200724

CCc1nn(C)c(C(=O)O)c1Cl.Cl

nearest known ligand 0.46

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
GAA known ✓ P10253 2/20 0.38
NR3C1 known ✓ P04150 2/20 0.35
RAB9A P51151 6/20 0.46
NPC1 O15118 5/20 0.46
LMNA P02545 5/20 0.44
SMN1; SMN2 Q16637 5/20 0.40
L3MBTL1 Q9Y468 3/20 0.40
ATM Q13315 2/20 0.40
POLB P06746 2/20 0.40
KDM4E B2RXH2 2/20 0.40
MAPT P10636 4/20 0.39
ALDH1A1 P00352 1/20 0.39
HTT P42858 1/20 0.38
NR1I2 O75469 1/20 0.38
AHR P35869 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
CYP2C9 P11712 1/20 0.36
GFER P55789 1/20 0.36
MAPK8 P45983 1/20 0.33
MAPK9 P45984 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
SCHEMBL4768937 0.98 RAB9A (0.47) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL28842596 0.86 RAB9A (0.42) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL9043817 0.84 LMNA (0.45) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL30356279 0.82 LMNA (0.44) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL15209660 0.81 LMNA (0.43) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL974535 0.78 LMNA (0.44) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL24553584 0.76 L3MBTL1 (0.39) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL6819929 0.76 MAPT (0.39) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL15825839 0.76 GAA (0.43) RAB9ANPC1LMNASMN1; SMN2L3MBTL1
SCHEMBL29732371 0.76 POLB (0.39) RAB9ANPC1LMNASMN1; SMN2L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103360314-A New preparation method of tebufenpyrad UNIV ZHEJIANG TECHNOLOGY 2013-10-23 CN disclosed
CN-103351340-A Novel preparation method of tolfenpyrad UNIV ZHEJIANG TECHNOLOGY 2013-10-16 CN disclosed
EP-0365925-B1 Pyrazole amides and insecticide and miticide containing them as active ingredient MITSUBISHI CHEM CORP (JP) 1995-07-19 EP disclosed
US-5366991-A Agriculture ENI CHEM SYNTHESIS S.P.A. (IT) 1994-11-22 US disclosed
EP-0590720-A1 Pyrazolecarboxamides exhibiting insecticidal and acaricidal activity MINISTERO DELL' UNIVERSITA' E DELLA RICERCA SCIENTIFICA E TECNOLOGICA (IT) 1994-04-06 EP disclosed
US-5039693-A Pyrazole amides and insecticide and miticide containing them as active ingredient MITSUBISHI KASEI CORPORATION (JP) 1991-08-13 US disclosed
EP-0365925-A1 Pyrazole amides and insecticide and miticide containing them as active ingredient Mitsubishi Chemical Corporation (JP) 1990-05-02 EP disclosed