Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1592741

CN(C)Cc1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1.Cl

nearest known ligand 0.96

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
GAA known ✓ P10253 2/20 0.96
CA2 known ✓ P00918 2/20 0.50
ALDH1A1 P00352 7/20 0.96
TSHR P16473 3/20 0.96
LMNA P02545 2/20 0.96
MAPK1 P28482 3/20 0.61
MAPT P10636 3/20 0.61
KDM4E B2RXH2 3/20 0.61
SMN1; SMN2 Q16637 2/20 0.61
HPGD P15428 1/20 0.61
HTT P42858 1/20 0.61
CYP1A2 P05177 3/20 0.52
MEN1 O00255 3/20 0.52
KMT2A Q03164 3/20 0.52
CYP3A4 P08684 2/20 0.52
BLM P54132 2/20 0.52
ATM Q13315 2/20 0.52
HIF1A Q16665 2/20 0.52
NPSR1 Q6W5P4 2/20 0.52
CYP2C9 P11712 2/20 0.52

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
SCHEMBL38719 0.98 ALDH1A1 (1.00) ALDH1A1TSHRLMNAGAAMAPK1
SCHEMBL30343310 0.96 ALDH1A1 (0.96) ALDH1A1TSHRLMNAGAAMAPK1
SCHEMBL25308455 0.96 ALDH1A1 (0.96) ALDH1A1TSHRLMNAGAAMAPK1
SCHEMBL25307340 0.96 ALDH1A1 (0.96) ALDH1A1TSHRLMNAGAAMAPK1
SCHEMBL25262628 0.96 ALDH1A1 (0.96) ALDH1A1TSHRLMNAGAAMAPK1
Boric Acid SCHEMBL9665661 0.92 ALDH1A1 (0.89) ALDH1A1TSHRLMNAGAAMAPK1
SCHEMBL11636500 0.92 ALDH1A1 (0.89) ALDH1A1TSHRLMNAGAAMAPK1
SCHEMBL9345626 0.91 ALDH1A1 (0.86) ALDH1A1TSHRLMNAGAAMAPK1
Hydrochloric Acid SCHEMBL8844291 0.88 ALDH1A1 (0.75) ALDH1A1TSHRLMNAGAAMAPK1
Catechol SCHEMBL9664944 0.88 ALDH1A1 (0.80) ALDH1A1TSHRLMNAGAAMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-5085932-A None JP disclosed
US-20240409563-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. 2024-12-12 US disclosed
EP-4448536-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. (US) 2024-10-23 EP disclosed
CN-118401532-A High-purity polysiloxane macromer and preparation method thereof 盖列斯特有限公司 2024-07-26 CN disclosed
WO-2023113779-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. (US) 2023-06-22 WO disclosed
US-20230183273-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. 2023-06-15 US disclosed
US-9018332-B2 Polyorganosiloxane containing methacryloxy group or acryloxy group and method for producing the same DOW CORNING TORAY COMPANY, LTD. (JP) 2015-04-28 US disclosed
US-20110092660-A1 Polyorganosiloxane Containing Methacryloxy Group Or Acryloxy Group And Method For Producing The Same DOW CORNING TORAY COMPANY, LTD. (JP) 2011-04-21 US disclosed
EP-2251370-A1 POLYORGANOSILOXANE CONTAINING METHACRYLOXY GROUP OR ACRYLOXY GROUP AND METHOD FOR PRODUCING THE SAME Dow Corning Toray Co., Ltd. (JP) 2010-11-17 EP disclosed
US-6197988-B1 DECOMPOSITION IN PRESENCE OF LEWIS ACID METAL HALIDE DOW CORNING TORAY SILICONE CO., LTD. (JP) 2001-03-06 US disclosed
EP-0722723-A2 Phenol derivatives for treating multiple sclerosis ELI LILLY AND COMPANY (US) 1996-07-24 EP disclosed
EP-0680755-A1 Method for treating inflammation, ischemia-induced cell damage and muscular dystrophy ELI LILLY AND COMPANY (US) 1995-11-08 EP disclosed
EP-0474403-B1 Method of treating inflammatory bowel disease LILLY CO ELI (US) 1995-05-10 EP disclosed
US-5393786-A Administering certain phenolic compounds ELI LILLY AND COMPANY (US) 1995-02-28 US disclosed
US-5281623-A Administering amino substituted phenolic derivatives as antiinflammatory or antiarthritic agents ELI LILLY AND COMPANY (US) 1994-01-25 US disclosed
US-5280046-A Using an amide containing phenol compound THE UNIVERSITY OF COLORADO FOUNDATION, INC. (US) 1994-01-18 US disclosed
JP-H0585932-A THERAPEUTIC MEDICINE FOR TYPE I DIABETES UNIV COLORADO FOUND INC 1993-04-06 JP disclosed
EP-0500336-A1 Composition containing certain phenol and benzamide for the treatment of type I diabetes UNIVERSITY OF COLORADO FOUNDATION, INC. (US) 1992-08-26 EP disclosed
EP-0476846-A2 Method for treating imflammation, ischemia-induced cell damage and muscular dystrophy ELI LILLY AND COMPANY (US) 1992-03-25 EP disclosed
EP-0474403-A1 Method of treating inflammatory bowel disease ELI LILLY AND COMPANY (US) 1992-03-11 EP 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 (2 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-20240409563-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME SSRP1, RPLP2, RPLP1 GAA 3157/4885CA2 3843/4885ALDH1A1 837/4885
US-20230183273-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME SSRP1, RPLP2, RPLP1 GAA 3157/4885CA2 3843/4885ALDH1A1 837/4885

“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.