Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7306548

CN1[C@@H]2CC[C@H]1C[C@@H](NC(=O)c1n[nH]c3ccccc3c1=O)C2.Cl

nearest known ligand 0.83

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
HTR3A known ✓ P46098 10/20 0.64
HTR3E known ✓ A5X5Y0 5/20 0.64
HTR3B known ✓ O95264 5/20 0.64
HTR3D known ✓ Q70Z44 5/20 0.64
HTR3C known ✓ Q8WXA8 5/20 0.64
CHRNA3 known ✓ P32297 1/20 0.53
KCNH2 known ✓ Q12809 1/20 0.53
ALDH1A1 P00352 1/20 0.58
CYP3A4 P08684 1/20 0.58
TSHR P16473 1/20 0.58
MAPK1 P28482 1/20 0.58
HSD17B10 Q99714 1/20 0.58
GSK3B P49841 1/20 0.58
DYRK1A Q13627 1/20 0.58
NPC1 O15118 1/20 0.56
RAB9A P51151 1/20 0.56
SLC22A2 O15244 1/20 0.53
CHRNB2 P17787 1/20 0.53
CHRNA4 P43681 1/20 0.53
SLC47A1 Q96FL8 1/20 0.53

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
Hydrochloric Acid SCHEMBL7306552 1.00 HTR3A (0.64) HTR3AHTR3EHTR3BHTR3DHTR3C
SCHEMBL2086084 0.91 NPC1 (0.67) HTR3AHTR3EHTR3BHTR3DHTR3C
SCHEMBL2087490 0.87 NPC1 (0.68) HTR3AHTR3EHTR3BHTR3DHTR3C
SCHEMBL12441936 0.87 NPC1 (0.68) HTR3AHTR3EHTR3BHTR3DHTR3C
SCHEMBL2086948 0.87 NPC1 (0.68) HTR3AHTR3EHTR3BHTR3DHTR3C
Trifluoroacetic Acid SCHEMBL17163423 0.85 NPC1 (0.60) HTR3AHTR3EHTR3BHTR3DHTR3C
Trifluoroacetic Acid SCHEMBL17163426 0.85 NPC1 (0.60) HTR3AHTR3EHTR3BHTR3DHTR3C
SCHEMBL19236410 0.85 NPC1 (0.62) HTR3AHTR3EHTR3BHTR3DHTR3C
Indisetron SCHEMBL2229963 0.83 NPC1 (0.60) HTR3AHTR3EHTR3BHTR3DHTR3C
Indisetron SCHEMBL15313306 0.83 NPC1 (0.60) HTR3AHTR3EHTR3BHTR3DHTR3C

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
EP-0560604-B1 Cinnoline-3-carboxylic acid derivatives as 5-HT3 antagonists MITSUBISHI CHEM CORP (JP) 1997-01-29 EP disclosed
US-5556851-A TREATMENT OF NAUSEA OR EMESIS FROM ANTICANCER DRUGS OR X-RAY TREATMENT MITSUBISHI CHEMICAL CORPORATION (JP) 1996-09-17 US disclosed
US-5391549-A Antagonistifc activity against serotonin 5HT3 receptors MITSUBISHI KASEI CORPORATION (JP) 1995-02-21 US disclosed
EP-0560604-A1 Cinnoline-3-carboxylic acid derivatives as 5-HT3 antagonists Mitsubishi Chemical Corporation (JP) 1993-09-15 EP disclosed