Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7624072

CC(=CC=Nc1ccccc1)CC=Nc1ccccc1.Cl

nearest known ligand 0.35

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
CACNA1B known ✓ Q00975 1/20 0.35
GAA known ✓ P10253 3/20 0.32
GLA known ✓ P06280 1/20 0.32
KMT2A Q03164 13/20 0.35
MEN1 O00255 9/20 0.35
NOS3 P29474 2/20 0.35
NOS1 P29475 2/20 0.35
MAPT P10636 7/20 0.35
ALDH1A1 P00352 4/20 0.35
POLB P06746 4/20 0.35
APBA1 Q02410 1/20 0.35
S100B P04271 1/20 0.32
RECQL P46063 3/20 0.32
MAPK1 P28482 2/20 0.32
CTNNB1 P35222 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
KDM4E B2RXH2 4/20 0.32
LMNA P02545 2/20 0.32
NPSR1 Q6W5P4 2/20 0.32
THRB P10828 1/20 0.32

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
SCHEMBL8607892 0.98 NOS3 (0.36) KMT2AMEN1NOS3NOS1MAPT
SCHEMBL9112452 0.98 NOS3 (0.36) KMT2AMEN1NOS3NOS1MAPT
Bromide SCHEMBL7703398 0.96 NOS3 (0.38) KMT2AMEN1NOS3NOS1MAPT
SCHEMBL13035384 0.79 NOS3 (0.39) KMT2AMEN1NOS3NOS1MAPT
SCHEMBL8603549 0.79 ALDH1A1 (0.33) KMT2AMEN1NOS3NOS1MAPT
SCHEMBL9318402 0.74 NOS1 (0.47) KMT2AMEN1NOS3NOS1MAPT
SCHEMBL9869506 0.72 ALDH1A1 (0.36) KMT2AMEN1NOS3NOS1MAPT
Hydrochloric Acid SCHEMBL2960051 0.71 ALDH1A1 (0.43) KMT2AMEN1NOS3NOS1MAPT
Hydrochloric Acid SCHEMBL2960053 0.71 ALDH1A1 (0.43) KMT2AMEN1NOS3NOS1MAPT
SCHEMBL10031422 0.69 NOS3 (0.36) KMT2AMEN1NOS3NOS1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6441191-B1 INFRARED ABSORBING AGENTS IN COLLOIDAL LAYERS FOR PHOTOGRAPHIC RECORDING MATERIALS; LONG WAVELENGTH; INTENSE ABSORPTION HONEYWELL INTERNATIONAL INC. 2002-08-27 US disclosed
US-6261753-B1 INFRARED RADIATION ABSORBERS; PHOTOGRAPHIC RECORDING MATERIALS RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) 2001-07-17 US disclosed
EP-0694586-B1 Use of indoleninecyaninedisulfonic acid derivatives as infrared absorbing compounds RIEDEL DE HAEN GMBH (DE) 2000-04-19 EP disclosed
US-5747233-A INFRARED ABSORBERS AND PHOTOGRAPHY RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) 1998-05-05 US disclosed
EP-0694586-A1 Use of indoleninecyaninedisulfonic acid derivatives as infrared absorbing compounds RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) 1996-01-31 EP disclosed
US-5106990-A Absorb infrared radiation, discolor during photographic development FUJI PHOTO FILM CO., LTD. (JP) 1992-04-21 US disclosed
US-4839265-A HYDROPHILIC COLLOID CONTAINING WATER SOLUBLE DYE FUJI PHOTO FILM CO., LTD. (JP) 1989-06-13 US disclosed