Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4679683

Cl.Oc1cc(NNF)ccc1Cl

nearest known ligand 0.45

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
▸ GLA known ✓ P06280 1/20 0.38
▸ KDR known ✓ P35968 2/20 0.35
▸ MAOB known ✓ P27338 1/20 0.35
▸ RET known ✓ P07949 1/20 0.35
▸ EGFR known ✓ P00533 1/20 0.34
▸ HSD17B10 Q99714 3/20 0.45
▸ TSHR P16473 2/20 0.45
▸ ALDH1A1 P00352 2/20 0.45
▸ CYP3A4 P08684 2/20 0.45
▸ TDP1 Q9NUW8 1/20 0.45
▸ MAPT P10636 2/20 0.38
▸ KIF5B P33176 1/20 0.35
▸ HPGD P15428 1/20 0.34
▸ EPHX1 P07099 1/20 0.34
▸ EPHX2 P34913 1/20 0.34
▸ RIPK2 O43353 1/20 0.34
▸ TGFBR1 P36897 1/20 0.34
▸ MEN1 O00255 1/20 0.33
▸ NPC1 O15118 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
SCHEMBL6321756 0.98 HSD17B10 (0.46) HSD17B10TSHRALDH1A1CYP3A4TDP1
Sulfuric Acid SCHEMBL6321163 0.89 HSD17B10 (0.39) HSD17B10TSHRALDH1A1CYP3A4TDP1
Hydrochloric Acid SCHEMBL8073459 0.82 HSD17B10 (0.46) HSD17B10TSHRALDH1A1CYP3A4TDP1
SCHEMBL7568541 0.79 HSD17B10 (0.48) HSD17B10TSHRALDH1A1CYP3A4TDP1
SCHEMBL1702377 0.78 HSD17B10 (0.46) HSD17B10TSHRALDH1A1CYP3A4TDP1
SCHEMBL10561861 0.73 SNCA (0.36) ALDH1A1MAPTKDRMEN1POLB
SCHEMBL15934314 0.72 HSD17B10 (0.50) HSD17B10TSHRALDH1A1CYP3A4TDP1
SCHEMBL5159903 0.71 LMNA (0.44) HSD17B10TSHRALDH1A1CYP3A4TDP1
SCHEMBL7972825 0.69 GRM4 (0.46) TSHRALDH1A1GAAMAPTGLA
SCHEMBL3163483 0.69 ALDH1A1 (0.42) HSD17B10TSHRALDH1A1CYP3A4TDP1

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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0850227-B1 PYRIDAZIN-3-ONE DERIVATIVES, THEIR USE, AND INTERMEDIATES FOR THEIR PRODUCTION SUMITOMO CHEMICAL CO (JP) 2008-01-09 — — EP disclosed
CN-1252066-C Pyridazine-3-one derivatives, their use, and intermediate preparing them SUMITOMO CHEMICAL CO (JP) 2006-04-19 — — CN disclosed
US-6869913-B1 Pyridazin-3-one derivatives, their use and intermediates for their production SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-03-22 — — US disclosed
US-6852890-B1 Process for the preparation of phenylhydrazines SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-02-08 — — US disclosed
EP-1175393-B1 PROCESS FOR THE PREPARATION OF PHENYLHYDRAZINES SUMITOMO CHEMICAL CO (JP) 2004-06-09 — — EP disclosed
CN-1491949-A Pyridazine-3-one derivatives, their use, and intermediate preparing them ס�ѻ�ѧ��ҵ��ʽ���� 2004-04-28 — — CN disclosed
US-6703503-B2 HERBICIDES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-03-09 — — US disclosed
US-20040005986-A1 Pyridazin-3-one derivatives, their use, and intermediates for their production SUMITOMO CHEMICAL COMPANY, LIMITED 2004-01-08 — — US disclosed
CN-1117083-C Pyridazin-3-one derivatives, their use, and intermediates for their preparation SUMITOMO CHEMICAL CO (JP) 2003-08-06 — — CN disclosed
US-6482773-B1 Pyridazin-3-one derivatives, their use, and intermediates for their production SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-11-19 — — US disclosed
WO-2001066513-A1 PROCESS FOR THE PREPARATION OF PHENYLHYDRAZINES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-09-13 — — WO disclosed
US-6107250-A 2-(SUBSTITUTED PHENYL),5-HALOALKYL-PYRIDAZIN-3-ONE DERIVATIVES AS HERBICIDES; NONPHYTOTOXIC; CONTROLLING WEEDS SUMITOMO CHEMICAL COMPANY LIMITED (JP) 2000-08-22 — — US disclosed
US-6090753-A 2-(SUBSTITUTED PHENYL), 5-HALOALKYL-PYRIDAZIN-3-ONE DERIVATIVES AS HERBICIDES; CONTROLLING WEEDS, METHOD OF MAKING BY REACTING A HYDRAZONE DERIVATIVE WITH A SPECIFIED PHOSPHORUS COMPOUND SUMITOMO CHEMICAL COMPANY LIMITED (JP) 2000-07-18 — — US disclosed
CN-1202157-A Pyridazin-3-one derivatives, their use, and intermediates for their preparation SUMITOMO CHEMICAL CO (JP) 1998-12-16 — — CN disclosed
CN-1199732-A Pyridazin-3-one derivatives and their use SUMITOMO CHEMICAL CO (JP) 1998-11-25 — — CN disclosed
CN-1196353-A Pyridazin-3-one derivatives and their use SUMITOMO CHEMICAL CO (JP) 1998-10-21 — — CN disclosed
EP-0860435-A1 Pyridazin-3-one derivatives and their use SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1998-08-26 — — EP disclosed
EP-0860434-A1 Pyridazin-3-one derivatives and their use SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1998-08-26 — — EP disclosed
EP-0850227-A1 PYRIDAZIN-3-ONE DERIVATIVES, THEIR USE, AND INTERMEDIATES FOR THEIR PRODUCTION SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1998-07-01 — — EP disclosed
WO-1997007104-A1 PYRIDAZIN-3-ONE DERIVATIVES, THEIR USE, AND INTERMEDIATES FOR THEIR PRODUCTION SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1997-02-27 — — WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040005986-A1 Pyridazin-3-one derivatives, their use, and intermediates for their production Q6ZSR9, HDHD5, CBR3 GAA 2089/4885GLA 1362/4885KDR 3240/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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