Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3292729

CCC1=C(C)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(C)c5CC)C(C)=C4CCC(=O)O)c(CCC(=O)O)c3C.Cl.Cl.[SnH2]

nearest known ligand 0.61

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 3/20 0.33
▸ EGFR known ✓ P00533 2/20 0.32
▸ HSD17B10 Q99714 3/20 0.61
▸ TDP1 Q9NUW8 3/20 0.61
▸ MEN1 O00255 2/20 0.61
▸ MAPT P10636 2/20 0.61
▸ THRB P10828 2/20 0.61
▸ MAPK1 P28482 2/20 0.61
▸ KMT2A Q03164 2/20 0.61
▸ APEX1 P27695 2/20 0.61
▸ USP2 O75604 1/20 0.61
▸ LMNA P02545 1/20 0.61
▸ CYP1A2 P05177 1/20 0.61
▸ POLB P06746 1/20 0.61
▸ CYP2D6 P10635 1/20 0.61
▸ HSPD1 P10809 1/20 0.61
▸ CYP2C9 P11712 1/20 0.61
▸ HPGD P15428 1/20 0.61
▸ ALOX15 P16050 1/20 0.61
▸ NFKB1 P19838 1/20 0.61

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
Hydrochloric Acid SCHEMBL1044115 0.99 HSD17B10 (0.62) HSD17B10TDP1MEN1MAPTTHRB
Hydrochloric Acid SCHEMBL1042399 0.99 HSD17B10 (0.62) HSD17B10TDP1MEN1MAPTTHRB
Hydrochloric Acid SCHEMBL1044825 0.99 HSD17B10 (0.62) HSD17B10TDP1MEN1MAPTTHRB
Hydrochloric Acid SCHEMBL6414612 0.98 HSD17B10 (0.61) HSD17B10TDP1MEN1MAPTTHRB
Hydrochloric Acid SCHEMBL3287063 0.98 HSD17B10 (0.61) HSD17B10TDP1MEN1MAPTTHRB
SCHEMBL9609762 0.98 HSD17B10 (0.63) HSD17B10TDP1MEN1MAPTTHRB
SCHEMBL5447002 0.98 HSD17B10 (0.63) HSD17B10TDP1MEN1MAPTTHRB
SCHEMBL6413992 0.98 HSD17B10 (0.63) HSD17B10TDP1MEN1MAPTTHRB
SCHEMBL314687 0.98 HSD17B10 (0.63) HSD17B10TDP1MEN1MAPTTHRB
SCHEMBL1602993 0.97 HSD17B10 (0.62) HSD17B10TDP1MEN1MAPTTHRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7527904-B2 Imaging member XEROX CORPORATION (US) 2009-05-05 — — US claimed
US-7399565-B2 Substrate; undercoat containing optionally doped TiO2 and meso-Tetraphenylporphine-4,4',4'',4'''-tetracarboxylic acid; and a charge transport layer; additive eliminates charge deficient spots in specific conditions and improves image quality. XEROX CORPORATION (US) 2008-07-15 — — US claimed
US-20070218377-A1 electrophotography; eliminates ghosting, improves image quality XEROX CORPORATION (US) 2007-09-20 — — US claimed
US-20070141490-A1 Imaging member U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2007-06-21 — — US claimed
US-20070092816-A1 Imaging member having porphine additive XEROX CORPORATION (US) 2007-04-26 — — US claimed
US-7718334-B2 Imaging member having porphine or porphine derivatives XEROX CORPORATION (US) 2010-05-18 — — US disclosed
US-7527904-B2 Imaging member XEROX CORPORATION (US) 2009-05-05 — — US disclosed
US-7399565-B2 Substrate; undercoat containing optionally doped TiO2 and meso-Tetraphenylporphine-4,4',4'',4'''-tetracarboxylic acid; and a charge transport layer; additive eliminates charge deficient spots in specific conditions and improves image quality. XEROX CORPORATION (US) 2008-07-15 — — US disclosed
US-20070218377-A1 electrophotography; eliminates ghosting, improves image quality XEROX CORPORATION (US) 2007-09-20 — — US disclosed
US-20070141490-A1 Imaging member U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2007-06-21 — — US disclosed
US-20070092816-A1 Imaging member having porphine additive XEROX CORPORATION (US) 2007-04-26 — — US disclosed
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