Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4552003

Cl.Cl.O=C(Nc1ccc(CCNCc2cccc(Cl)c2)cc1)c1cccs1

nearest known ligand 0.65

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
HDAC1 known ✓ Q13547 1/20 0.52
ABL1 known ✓ P00519 1/20 0.50
NOS3 P29474 3/20 0.65
NOS1 P29475 2/20 0.63
NOS2 P35228 2/20 0.63
NPC1 O15118 4/20 0.61
RAB9A P51151 4/20 0.61
HTT P42858 3/20 0.61
SMN1; SMN2 Q16637 2/20 0.61
SLC2A1 P11166 2/20 0.57
LMNA P02545 1/20 0.55
MAPT P10636 3/20 0.55
KDM4E B2RXH2 2/20 0.55
POLB P06746 1/20 0.55
CYP1A2 P05177 2/20 0.54
CYP3A4 P08684 2/20 0.54
CYP2D6 P10635 2/20 0.54
CYP2C19 P33261 2/20 0.54
MEN1 O00255 4/20 0.53
KMT2A Q03164 4/20 0.53

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
SCHEMBL3264531 0.99 NOS3 (0.64) NOS3NOS1NOS2NPC1RAB9A
Hydrochloric Acid SCHEMBL31114391 0.87 NOS3 (0.65) NOS3NOS1NOS2NPC1RAB9A
SCHEMBL29558856 0.86 NOS3 (0.64) NOS3NOS1NOS2NPC1RAB9A
SCHEMBL122445 0.86 NOS3 (0.64) NOS3NOS1NOS2NPC1RAB9A
SCHEMBL6967975 0.80 NOS3 (0.57) NOS3NOS1NOS2NPC1RAB9A
SCHEMBL579839 0.80 NPC1 (0.61) NPC1RAB9ASMN1; SMN2LMNAKDM4E
SCHEMBL3954529 0.80 MAPK1 (0.56) NOS3NOS1NOS2NPC1RAB9A
Hydrochloric Acid SCHEMBL30007714 0.79 NOS3 (1.00) NOS3NOS1NOS2
SCHEMBL6967589 0.77 NOS3 (0.59) NOS3NOS1NOS2NPC1RAB9A
SCHEMBL122446 0.77 NOS3 (1.00) NOS3NOS1NOS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024059834-A2 DOWNREGULATING INOS TO INCREASE CAR-T KILLING H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE INC. (US) 2024-03-21 WO claimed
US-20090186929-A1 Method and agent for inducing apoptosis/cell death in leukemia cells U.S. DEPARTMENT OF VETERANS AFFAIRS (US) 2009-07-23 US claimed
US-20050234026-A1 Method and agent for inducing apoptosis/cell death in leukemia cells VETERANS AFFAIRS, U.S. DEPARTMENT OF 2005-10-20 US claimed
US-20090186929-A1 Method and agent for inducing apoptosis/cell death in leukemia cells U.S. DEPARTMENT OF VETERANS AFFAIRS (US) 2009-07-23 US disclosed
US-20050234026-A1 Method and agent for inducing apoptosis/cell death in leukemia cells VETERANS AFFAIRS, U.S. DEPARTMENT OF 2005-10-20 US disclosed