Hydrochloric Acid

Hydrochloric Acid

SCHEMBL659782

CCOc1ccc(-c2nc3cc(-c4nc5cc(N6CCN(C)CC6)ccc5[nH]4)ccc3[nH]2)cc1.Cl.Cl.Cl.Cl.Cl.Cl

nearest known ligand 0.79

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
▸ GLA known ✓ P06280 1/20 0.79
▸ TOP1 known ✓ P11387 3/20 0.62
▸ TOP2A known ✓ P11388 3/20 0.62
▸ DRD3 known ✓ P35462 5/20 0.51
▸ DRD2 known ✓ P14416 4/20 0.50
▸ GAA known ✓ P10253 1/20 0.48
▸ KCNH2 known ✓ Q12809 1/20 0.48
▸ MAOB known ✓ P27338 1/20 0.48
▸ ALDH1A1 P00352 5/20 0.79
▸ SMN1; SMN2 Q16637 4/20 0.79
▸ MAPT P10636 3/20 0.79
▸ MEN1 O00255 2/20 0.79
▸ BLM P54132 2/20 0.79
▸ KMT2A Q03164 2/20 0.79
▸ SLCO2B1 O94956 1/20 0.79
▸ RECQL P46063 1/20 0.79
▸ BCL2L1 Q07817 1/20 0.79
▸ SLCO1B3 Q9NPD5 1/20 0.79
▸ TDP1 Q9NUW8 1/20 0.79
▸ SLCO1B1 Q9Y6L6 1/20 0.79

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 SCHEMBL38685 1.00 ALDH1A1 (0.79) ALDH1A1SMN1; SMN2MAPTMEN1BLM
Hydrochloric Acid SCHEMBL29728780 1.00 ALDH1A1 (0.79) ALDH1A1SMN1; SMN2MAPTMEN1BLM
Hydrochloric Acid SCHEMBL6850585 1.00 ALDH1A1 (0.79) ALDH1A1SMN1; SMN2MAPTMEN1BLM
Hydrochloric Acid SCHEMBL4538254 0.99 ALDH1A1 (0.78) ALDH1A1SMN1; SMN2MAPTMEN1BLM
Hydrochloric Acid SCHEMBL15545820 0.99 ALDH1A1 (0.78) ALDH1A1SMN1; SMN2MAPTMEN1BLM
Hydrochloric Acid SCHEMBL4950608 0.99 ALDH1A1 (0.78) ALDH1A1SMN1; SMN2MAPTMEN1BLM
SCHEMBL29466902 0.99 ALDH1A1 (0.81) ALDH1A1SMN1; SMN2MAPTMEN1BLM
SCHEMBL1059266 0.99 ALDH1A1 (0.81) ALDH1A1SMN1; SMN2MAPTMEN1BLM
Hoechst 33258 SCHEMBL6942659 0.94 ALDH1A1 (0.71) ALDH1A1SMN1; SMN2MAPTMEN1BLM
SCHEMBL15969230 0.94 ALDH1A1 (0.90) ALDH1A1SMN1; SMN2MAPTMEN1BLM

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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11931713-B2 Oligonucleotide data storage on solid supports Global Life Sciences Solutions Operations UK Ltd (GB) 2024-03-19 — — US disclosed
US-20230167197-A1 ANTI-CERAMIDE ANTIBODIES MEMORIAL SLOAN KETTERING CANCER CENTER (US) 2023-06-01 — — US disclosed
CN-115811987-A Anti-ceramide antibodies 纪念斯隆凯特琳癌症中心 2023-03-17 — — CN disclosed
EP-4121110-A1 ANTI-CERAMIDE ANTIBODIES Memorial Sloan Kettering Cancer Center (US) 2023-01-25 — — EP disclosed
WO-2021188770-A1 ANTI-CERAMIDE ANTIBODIES MEMORIAL SLOAN KETTERING CANCER CENTER (US) 2021-09-23 — — WO disclosed
US-20170151545-A1 OLIGONUCLEOTIDE DATA STORAGE ON SOLID SUPPORTS Global Life Sciences Solutions Operations UK Ltd (GB) 2017-06-01 — — US disclosed
WO-2015090879-A1 OLIGONUCLEOTIDE DATA STORAGE ON SOLID SUPPORTS GE HEALTHCARE UK LIMITED (GB) 2015-06-25 — — WO disclosed
US-20120045501-A1 CONNEXIN ENHANCES CHEMOTHERAPY-INCLUDED APOPTOSIS IN HUMAN CANCER CELLS INHIBITING TUMOR CELL PROLIFERATION NORTHWEST HOSPITAL (US) 2012-02-23 — — US disclosed
EP-1729788-B1 RESTENOSIS THERAPY USING MESENCHYMAL STEM CELLS BOSTON SCIENT LTD (BB) 2009-11-25 — — EP disclosed
US-20080138337-A1 CONNEXIN ENHANCES CHEMOTHERAPY-INDUCED APOPTOSIS IN HUMAN CANCER CELLS INHIBITING TUMOR CELL PROLIFERATION NORTHWEST HOSPITAL (US) 2008-06-12 — — US disclosed
WO-2001050848-A2 CLONAL PROPAGATION OF PRIMATE OFFSPRING BY EMBRYO SPLITTING OREGON HEALTH AND SCIENCE UNIVERSITY (US) 2001-07-19 — — WO disclosed
EP-1017421-A1 METHOD AND COMPOSITIONS FOR HEALING TISSUE DEFECTS AND INDUCING HYPERVASCULARITY IN MAMMALIAN TISSUE THE WISTAR INSTITUTE OF ANATOMY AND BIOLOGY (US) 2000-07-12 — — EP disclosed
WO-1999061581-A2 SPHINGOSINE KINASE, CLONING, EXPRESSION AND METHODS OF USE OFFICE OF THE DEAN OF RESEARCH AND GRADUATE EDUCATION (US) 1999-12-02 — — WO disclosed
WO-1999007844-A2 METHODS AND COMPOSITIONS FOR TREATMENT OF RESTENOSIS THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1999-02-18 — — WO disclosed
EP-0888458-A1 COMBINATIONS OF PKC INHIBITORS AND THERAPEUTIC AGENTS FOR TREATING CANCERS Sloan-Kettering Institute For Cancer Research (US) 1999-01-07 — — EP disclosed
US-5821072-A SCREENING PROTEIN KINASE C INHIBITORS CAPABLE OF POTENTIATING APOPTOSIS IN TUMOR CELLS SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1998-10-13 — — US disclosed
WO-1998039035-A1 METHOD AND COMPOSITIONS FOR HEALING TISSUE DEFECTS AND INDUCING HYPERVASCULARITY IN MAMMALIAN TISSUE THE WISTAR INSTITUTE OF ANATOMY & BIOLOGY (US) 1998-09-11 — — WO disclosed
US-5744499-A Apoptosis-modulating factors influencing the intracellular concentration of methional/malondialdehyde CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES GALDERMA (FR) 1998-04-28 — — US disclosed
WO-1997030174-A1 COMBINATIONS OF PKC INHIBITORS AND THERAPEUTIC AGENTS FOR TREATING CANCERS SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1997-08-21 — — WO disclosed
WO-1990013627-A1 IN VITRO MATURATION OF BOVINE OOCYTES GRANADA BIOSCIENCES, INC. (US) 1990-11-15 — — WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080138337-A1 CONNEXIN ENHANCES CHEMOTHERAPY-INDUCED APOPTOSIS IN HUMAN CANCER CELLS INHIBITING TUMOR CELL PROLIFERATION GJA1, GJB2, BCL2 GLA 4763/4885TOP1 87/4885TOP2A 94/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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