Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6645397

Cl.O=C(O)Cc1ncccn1

nearest known ligand 0.48

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
GABRP known ✓ O00591 2/20 0.39
GABRD known ✓ O14764 2/20 0.39
GABRA1 known ✓ P14867 2/20 0.39
GABRB1 known ✓ P18505 2/20 0.39
GABRG2 known ✓ P18507 2/20 0.39
GABRB3 known ✓ P28472 2/20 0.39
GABRA5 known ✓ P31644 2/20 0.39
GABRA3 known ✓ P34903 2/20 0.39
GABRA2 known ✓ P47869 2/20 0.39
GABRB2 known ✓ P47870 2/20 0.39
GABRA4 known ✓ P48169 2/20 0.39
GABRE known ✓ P78334 2/20 0.39
GABRA6 known ✓ Q16445 2/20 0.39
GABRG1 known ✓ Q8N1C3 2/20 0.39
GABRG3 known ✓ Q99928 2/20 0.39
GABRQ known ✓ Q9UN88 2/20 0.39
GAA known ✓ P10253 1/20 0.37
PTGS1 known ✓ P23219 1/20 0.37
KDM4E B2RXH2 3/20 0.48
CYP1A2 P05177 2/20 0.48

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
SCHEMBL874090 0.97 CYP1A2 (0.50) KDM4ECYP1A2MAPTAKR1B1NAPRT
Furan SCHEMBL473513 0.85 CYP1A2 (0.42) KDM4ECYP1A2MAPTAKR1B1NAPRT
SCHEMBL5094342 0.79 P2RX7 (0.41) KDM4ECYP1A2MAPTNAPRTLMNA
Butyl Alcohol SCHEMBL27561770 0.79 ALDH1A1 (0.40) KDM4ECYP1A2MAPTALDH1A1HTT
Hydrochloric Acid SCHEMBL22775406 0.76 ALDH1A1 (0.47) KDM4ELMNAP4HTMALDH1A1
SCHEMBL6428658 0.75 CYP1A2 (0.43) KDM4ECYP1A2MAPTAKR1B1NAPRT
SCHEMBL7769482 0.75 P2RX7 (0.38) KDM4ECYP1A2MAPTNAPRTLMNA
SCHEMBL1719924 0.75 LMNA (0.47) KDM4ECYP1A2MAPTNAPRTLMNA
SCHEMBL77616 0.75 HTT (0.48) KDM4ECYP1A2MAPTP2RX7HTT
SCHEMBL8539040 0.75 P2RX7 (0.38) KDM4ECYP1A2MAPTNAPRTLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6806230-B1 NITROGEN COMPOUNDS SUCH AS N-METHYL-N-(2-METHYL-1-(4-TRIFLUORO METHYLPYRIMIDIN-5-YL)PROPYL)PHENYLACETAMIDE, USED FOR PREFERENTIAL CONTROL OF WEEDS KUMIAI CHEMICAL INDUSTRY CO., LTD. (JP) 2004-10-19 US disclosed
EP-1211246-B1 PYRIMIDINE DERIVATIVES AND HERBICIDES CONTAINING THE SAME KUMIAI CHEMICAL INDUSTRY CO (JP) 2004-02-25 EP disclosed
EP-1211246-A1 PYRIMIDINE DERIVATIVES AND HERBICIDES CONTAINING THE SAME KUMIAI CHEMICAL INDUSTRY CO., LTD. (JP) 2002-06-05 EP disclosed