Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2554902

CC12CC3(C)CC(C)(C1)CC(N)(C2)C3.Cl

nearest known ligand 0.55

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
GRIN1 known ✓ Q05586 2/20 0.55
GRIN2A known ✓ Q12879 2/20 0.55
GRIN2D known ✓ O15399 1/20 0.50
GRIN3B known ✓ O60391 1/20 0.50
ESR1 known ✓ P03372 1/20 0.50
ADRB3 known ✓ P13945 1/20 0.50
ACHE known ✓ P22303 1/20 0.50
OPRK1 known ✓ P41145 1/20 0.50
GRIN2B known ✓ Q13224 1/20 0.50
GRIN2C known ✓ Q14957 1/20 0.50
GRIN3A known ✓ Q8TCU5 1/20 0.50
LMNA P02545 2/20 0.55
PMP22 Q01453 1/20 0.55
NPSR1 Q6W5P4 1/20 0.55
SLC22A1 O15245 1/20 0.50
MTOR P42345 1/20 0.50
HTT P42858 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP2D6 P10635 1/20 0.50
CYP2C9 P11712 1/20 0.50

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
SCHEMBL656738 0.96 LMNA (0.52) LMNAGRIN1GRIN2APMP22NPSR1
Hydrochloric Acid SCHEMBL13736300 0.96
SCHEMBL6130386 0.93 LMNA (0.50) LMNAGRIN1GRIN2APMP22NPSR1
SCHEMBL17586276 0.93
Hydrochloric Acid SCHEMBL1071784 0.84 LMNA (0.43) LMNAGRIN1GRIN2APMP22NPSR1
Hydrochloric Acid SCHEMBL7325630 0.80 GRIN1 (0.42) LMNAGRIN1GRIN2APMP22NPSR1
SCHEMBL24243950 0.80 LMNA (0.41) LMNAGRIN1GRIN2APMP22NPSR1
SCHEMBL3332166 0.80 LMNA (0.41) LMNAGRIN1GRIN2APMP22NPSR1
SCHEMBL18543255 0.80 LMNA (0.41) LMNAGRIN1GRIN2APMP22NPSR1
SCHEMBL18543254 0.80 LMNA (0.41) LMNAGRIN1GRIN2APMP22NPSR1

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
EP-2555616-A1 PROCESS FOR THE PREPARATION OF MEMANTINE HYDROCHLORIDE Hetero Research Foundation (IN) 2013-02-13 EP claimed
WO-2011125062-A1 PROCESS FOR THE PREPARATION OF MEMANTINE HYDROCHLORIDE HETERO RESEARCH FOUNDATION (IN) 2011-10-13 WO claimed
CN-107334744-B Memantine hydrochloride medicine composition and preparation method thereof 湖南洞庭药业股份有限公司 2020-09-04 CN disclosed
CN-107334744-A Memantine pharmaceutical composition and preparation method 湖南洞庭药业股份有限公司 2017-11-10 CN disclosed
EP-2555616-A1 PROCESS FOR THE PREPARATION OF MEMANTINE HYDROCHLORIDE Hetero Research Foundation (IN) 2013-02-13 EP disclosed
EP-2555616-A1 PROCESS FOR THE PREPARATION OF MEMANTINE HYDROCHLORIDE Hetero Research Foundation (IN) 2013-02-13 EP disclosed
WO-2011125062-A1 PROCESS FOR THE PREPARATION OF MEMANTINE HYDROCHLORIDE HETERO RESEARCH FOUNDATION (IN) 2011-10-13 WO disclosed
WO-2011125062-A1 PROCESS FOR THE PREPARATION OF MEMANTINE HYDROCHLORIDE HETERO RESEARCH FOUNDATION (IN) 2011-10-13 WO disclosed
EP-1999100-A1 PROCESS FOR PREPARING MEMANTINE HYDROCHLORIDE SUBSTANTIALLY FREE OF IMPURITIES Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2008-12-10 EP disclosed
US-20080033054-A1 Process for preparing memantine hydrochloride substantially free of impurities TEVA PHARMACEUTICALS USA, INC. 2008-02-07 US disclosed
WO-2007126886-A1 PROCESS FOR PREPARING MEMANTINE HYDROCHLORIDE SUBSTANTIALLY FREE OF IMPURITIES TEVA PHARMACEUTICALS USA, INC. (US) 2007-11-08 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-20080033054-A1 Process for preparing memantine hydrochloride substantially free of impurities PNMT, PSEN2, CHRNA5 GRIN1 83/4885GRIN2A 16/4885GRIN2D 68/4885

“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.