Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1847744

CNC1CN(Cc2ccccc2)CCC1C.Cl.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 12)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 9/20 0.55
BCHE known ✓ P06276 9/20 0.51
SCN4A known ✓ P35499 2/20 0.47
SIGMAR1 known ✓ Q99720 2/20 0.45
BACE1 P56817 8/20 0.51
ALDH1A1 P00352 1/20 0.50
CYP1A2 P05177 1/20 0.47
CYP3A4 P08684 1/20 0.47
CYP2D6 P10635 1/20 0.47
CYP2C19 P33261 1/20 0.47
CCR3 P51677 1/20 0.46
CXCR4 P61073 1/20 0.44

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 SCHEMBL20597421 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
Hydrochloric Acid SCHEMBL1373413 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
Hydrochloric Acid SCHEMBL22500017 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
Hydrochloric Acid SCHEMBL29414409 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
Hydrochloric Acid SCHEMBL1373407 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
Hydrochloric Acid SCHEMBL2148084 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
Hydrochloric Acid SCHEMBL1375746 1.00 ACHE (0.55) ACHEBCHEBACE1ALDH1A1SCN4A
SCHEMBL1993388 0.98 ACHE (0.57) ACHEBCHEBACE1ALDH1A1SCN4A
SCHEMBL14018259 0.98 ACHE (0.57) ACHEBCHEBACE1ALDH1A1SCN4A
SCHEMBL352022 0.98 ACHE (0.57) ACHEBCHEBACE1ALDH1A1SCN4A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114835631-B Preparation method of cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 重庆恩联生物科技有限公司 2024-02-13 CN claimed
CN-112213402-B Method for detecting (3R, 4R) -1-benzyl-N, 4-dimethylpiperidine-3-amine dihydrochloride and isomer thereof 江苏晶立信医药科技有限公司 2022-11-04 CN claimed
CN-114835631-A Preparation method of cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 重庆恩联生物科技有限公司 2022-08-02 CN claimed
CN-107056681-B A kind of support method replaces the preparation method of cloth intermediate 广州白云山光华制药股份有限公司 2019-10-01 CN claimed
CN-107056681-A A kind of support method replaces the preparation method of cloth intermediate 广州白云山光华制药股份有限公司 2017-08-18 CN claimed
CN-105153166-A N- [ (3R,4R) -1-benzyl-4-methylpiperidin-3-yl ] -N-methyl-7H-pyrrolo [2,3-d ] pyrimidin-4-amine crystal HUBEI LIVSCIEN PHARM SCI & TECH CO LTD 2015-12-16 CN claimed
CN-114835631-B Preparation method of cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 重庆恩联生物科技有限公司 2024-02-13 CN disclosed
CN-114835631-B Preparation method of cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 重庆恩联生物科技有限公司 2024-02-13 CN disclosed
CN-114835631-B Preparation method of cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 重庆恩联生物科技有限公司 2024-02-13 CN disclosed
CN-113899831-B Liquid chromatography detection method for tofacitinib citrate starting material 湖北科益药业股份有限公司 2023-08-15 CN disclosed
CN-112213402-B Method for detecting (3R, 4R) -1-benzyl-N, 4-dimethylpiperidine-3-amine dihydrochloride and isomer thereof 江苏晶立信医药科技有限公司 2022-11-04 CN disclosed
CN-112213402-B Method for detecting (3R, 4R) -1-benzyl-N, 4-dimethylpiperidine-3-amine dihydrochloride and isomer thereof 江苏晶立信医药科技有限公司 2022-11-04 CN disclosed
CN-114835631-A Preparation method of cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 重庆恩联生物科技有限公司 2022-08-02 CN disclosed
EP-1666481-A2 OPTICAL RESOLUTION OF (1-BENZYL-4-METHYLPIPERIDIN-3-YL)-METHYLAMINE AND THE USE THEREOF FOR THE PREPARATION OF PYRROLO[2,3]PYRIMIDINE DERIVATIVES AS PROTEIN KINASES INHIBITORS Pfizer Products Incorporated (US) 2006-06-07 EP disclosed
CN-1729192-A Optical resolution of (1-benzyl-4-methylpiperidin-3-yl) -methylamine and the use thereof for the preparation of pyrrolo 2,3-pyrimidine derivatives as protein kinases inhibitors PFIZER PROD INC (US) 2006-02-01 CN disclosed
EP-1609781-A1 Optical resolution of (1-benzyl-4-methylpiperidin-3-yl)-methylamine Pfizer Products Incorporated (US) 2005-12-28 EP disclosed
US-20040229923-A1 Chiral salt resolution PFIZER INC. 2004-11-18 US disclosed
EP-1392694-A1 OPTICAL RESOLUTION OF (1-BENZYL-4-METHYLPIPERIDIN-3-YL)-METHYLAMINE AND THE USE THEREOF FOR THE PREPARATION OF PYRROLO[2,3]PYRIMIDINE DERIVATIVES AS PROTEIN KINASES INHIBITORS Pfizer Products Inc. (US) 2004-03-03 EP disclosed
US-20030073719-A1 Chiral salt resolution PFIZER INC. 2003-04-17 US disclosed
WO-2002096909-A1 OPTICAL RESOLUTION OF (1-BENZYL-4-METHYLPIPERIDIN-3-YL) -METHYLAMINE AND THE USE THEREOF FOR THE PREPARATION OF PYRROLO 2,3-PYRIMIDINE DERIVATIVES AS PROTEIN KINASES INHIBITORS PFIZER PRODUCTS INC. (US) 2002-12-05 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 (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-20040229923-A1 Chiral salt resolution REN, SRR, RER1 ACHE 2037/4885BCHE 1926/4885SCN4A 362/4885
US-20030073719-A1 Chiral salt resolution REN, SRR, RER1 ACHE 2037/4885BCHE 1926/4885SCN4A 362/4885

“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.