Hydrochloric Acid

Hydrochloric Acid

SCHEMBL27872175

Cl.O=C(O)Cc1cc(Cl)ccn1

nearest known ligand 0.43

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 1/20 0.43
▸ GABRD known ✓ O14764 1/20 0.43
▸ GABRA1 known ✓ P14867 1/20 0.43
▸ GABRB1 known ✓ P18505 1/20 0.43
▸ GABRG2 known ✓ P18507 1/20 0.43
▸ GABRB3 known ✓ P28472 1/20 0.43
▸ GABRA5 known ✓ P31644 1/20 0.43
▸ GABRA3 known ✓ P34903 1/20 0.43
▸ GABRA2 known ✓ P47869 1/20 0.43
▸ GABRB2 known ✓ P47870 1/20 0.43
▸ GABRA4 known ✓ P48169 1/20 0.43
▸ GABRE known ✓ P78334 1/20 0.43
▸ GABRA6 known ✓ Q16445 1/20 0.43
▸ GABRG1 known ✓ Q8N1C3 1/20 0.43
▸ GABRG3 known ✓ Q99928 1/20 0.43
▸ GABRQ known ✓ Q9UN88 1/20 0.43
▸ GAA known ✓ P10253 1/20 0.40
▸ CA2 known ✓ P00918 1/20 0.37
▸ MAPT P10636 2/20 0.42
▸ ALDH1A1 P00352 1/20 0.42

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
SCHEMBL7914812 0.98 GABRP (0.44) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL3186112 0.81 ALDH1A1 (0.46) MAPTALDH1A1L3MBTL1KDM4CNPC1
SCHEMBL1219394 0.81 ALDH1A1 (0.42) MAPTALDH1A1L3MBTL1KDM4CNPC1
SCHEMBL30405680 0.80 NR4A2 (0.49) MAPTALDH1A1L3MBTL1KDM4EPRNP
SCHEMBL17396955 0.79 KDM4E (0.53) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL27686130 0.78 GABRP (0.51) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL9993146 0.77 RAB9A (0.67) MAPTALDH1A1L3MBTL1NPC1RAB9A
SCHEMBL14552064 0.77 KMT2A (0.47) MAPTALDH1A1L3MBTL1KDM4EPRNP
SCHEMBL12815587 0.77 IDH1 (0.45) MAPTALDH1A1L3MBTL1KDM4CNPC1
SCHEMBL12815334 0.77 ALDH1A1 (0.46) MAPTALDH1A1L3MBTL1KDM4CNPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103087054-B 4-pyridine phenyl ether compounds and preparation method thereof and application SHANDONG UNIVERSITY (CN) 2015-12-23 — — CN claimed
CN-103087054-A 4-pyridyl phenyl ether compounds, and preparation method and application thereof UNIV SHANDONG 2013-05-08 — — CN claimed
CN-103087054-B 4-pyridine phenyl ether compounds and preparation method thereof and application SHANDONG UNIVERSITY (CN) 2015-12-23 — — CN disclosed
CN-104250226-A Method for preparing regorafenib intermediate IKON PHARMACEUTICALS LLC 2014-12-31 — — CN disclosed
CN-103087054-A 4-pyridyl phenyl ether compounds, and preparation method and application thereof UNIV SHANDONG 2013-05-08 — — CN disclosed
CN-102675197-A Method for preparing 4-chlorin-N-methylpyridine-2-formamide serving as sorafenib intermediate SHANGHAI AOBO BIO PHARMACEUTICAL TECH CO LTD 2012-09-19 — — CN disclosed
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