Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5672483

Cl.O=P(O)(O)C(C[n+]1ccccc1-c1ccccn1)P(=O)(O)O.[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
▸ CCR5 known ✓ P51681 2/20 0.34
▸ HDAC3 known ✓ O15379 1/20 0.31
▸ HDAC4 known ✓ P56524 1/20 0.31
▸ HDAC1 known ✓ Q13547 1/20 0.31
▸ HDAC7 known ✓ Q8WUI4 1/20 0.31
▸ HDAC2 known ✓ Q92769 1/20 0.31
▸ HDAC10 known ✓ Q969S8 1/20 0.31
▸ HDAC11 known ✓ Q96DB2 1/20 0.31
▸ HDAC8 known ✓ Q9BY41 1/20 0.31
▸ HDAC6 known ✓ Q9UBN7 1/20 0.31
▸ HDAC9 known ✓ Q9UKV0 1/20 0.31
▸ HDAC5 known ✓ Q9UQL6 1/20 0.31
▸ HSP90AA1 known ✓ P07900 1/20 0.31
▸ FDPS P14324 9/20 0.46
▸ GGPS1 O95749 5/20 0.35
▸ KDM4E B2RXH2 3/20 0.34
▸ P4HTM Q9NXG6 2/20 0.34
▸ LMNA P02545 2/20 0.34
▸ CCR1 P32246 2/20 0.34
▸ CCR8 P51685 2/20 0.34

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
SCHEMBL18768720 0.71 KDM4E (0.45) KDM4EP4HTMLMNACCR1CCR5
SCHEMBL2862221 0.71 KDM4E (0.45) KDM4EP4HTMLMNACCR1CCR5
SCHEMBL12060616 0.70 GGPS1 (0.39) FDPSGGPS1
Bromide SCHEMBL8599641 0.70 KDM4E (0.39) KDM4EP4HTMLMNACCR1CCR5
Iodide SCHEMBL8602274 0.70 KDM4E (0.39) KDM4EP4HTMLMNACCR1CCR5
Hydrochloric Acid SCHEMBL5671113 0.70 GGPS1 (0.40) FDPSGGPS1
Hydrochloric Acid SCHEMBL5672479 0.69 FDPS (0.36) FDPSKDM4EP4HTMLMNACCR1
SCHEMBL25526218 0.67 KDM4E (0.39) KDM4EP4HTMLMNACCR1CCR5
Dipyridyl SCHEMBL10772309 0.66 KDM4E (0.70) FDPSKDM4EP4HTMLMNACCR1
SCHEMBL16125566 0.66 KDM4E (0.50) KDM4EP4HTMLMNACCR1CCR5

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
EP-1004143-A4 CHARGE GENERATORS IN HETEROLAMELLAR MULTILAYER THIN FILMS UNIV SOUTHERN CALIFORNIA (US) 2006-04-12 — — EP disclosed
EP-1004143-A1 CHARGE GENERATORS IN HETEROLAMELLAR MULTILAYER THIN FILMS THE UNIVERSITY OF SOUTHERN CALIFORNIA (US) 2000-05-31 — — EP disclosed
WO-1999003154-A1 CHARGE GENERATORS IN HETEROLAMELLAR MULTILAYER THIN FILMS UNIVERSITY OF SOUTHERN CALIFORNIA (US) 1999-01-21 — — WO disclosed
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