Hydrochloric Acid

Hydrochloric Acid

SCHEMBL551204

CS(=O)(=O)CCN.Cl

nearest known ligand 0.00

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL141464 0.97
Sulfuric Acid SCHEMBL1556465 0.88 BLM (0.55)
SCHEMBL29145538 0.85 LMNA (0.39)
Hydrochloric Acid SCHEMBL3506692 0.81
Hydrochloric Acid SCHEMBL1448173 0.79
SCHEMBL1446201 0.78
Hydrochloric Acid SCHEMBL9985787 0.77 DNM1 (0.43)
Trifluoroacetic Acid SCHEMBL15049079 0.75 LMNA (0.37)
SCHEMBL460802 0.75
Hydrochloric Acid SCHEMBL20482978 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117998946-A Perovskite solar cell doped based on 2-aminoethyl methylsulfone hydrochloride and preparation method thereof 吉林大学 2024-05-07 CN claimed
CN-115108949-A Method for preparing 2- (methylsulfonyl) ethylamine hydrochloride by using methyl mercaptan 江苏恒沛药物科技有限公司 2022-09-27 CN claimed
WO-2022029795-A1 An environment friendly process for the preparation of Lapatinib Ditosylate of Formula 1(b) SUMAR BIOTECH LLP (IN) 2022-02-10 WO claimed
CN-110698417-B Preparation method of 6-substituent furyl-4-substituted amino quinazoline derivative and key intermediate thereof 新发药业有限公司 2020-11-20 CN claimed
WO-2020136671-A1 IMPROVED PROCESS FOR THE PREPARATION OF LAPATINIB BASE AND IT'S ANHYDROUS DITOSYLATE SALT NATCO PHARMA LIMITED (IN) 2020-07-02 WO claimed
CN-110698417-A Preparation method of 6-substituent furyl-4-substituted amino quinazoline derivative and key intermediate thereof 新发药业有限公司 2020-01-17 CN claimed
CN-105646405-B The preparation method of substituted adjacent amido benzonitrile compound, preparation method and Lapatinib 凯莱英医药集团(天津)股份有限公司 2018-12-11 CN claimed
CN-105738492-B The method of impurity content in LC MS/MS combination measure Lapatinibs 人福医药集团股份公司 2017-12-19 CN claimed
CN-107056661-A A kind of preparation method of lapatinib intermediate 2 (methylsulfonyl) ethylamine hydrochloride 山东铂源药业有限公司 2017-08-18 CN claimed
CN-105738492-A Method for detecting impurity content in lapatinib through combination of LC-MS and MS 人福医药集团股份公司 2016-07-06 CN claimed
CN-103030580-A Preparation method of lapatinib intermediate SHANDONG BOYUAN PHARMACEUTICAL CO LTD 2013-04-10 CN claimed
US-20120295928-A1 METHODS FOR DETECTING AND REDUCING IMPURITIES OF LAPATINIB AND SALTS THEREOF F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2012-11-22 US claimed
EP-2489661-A1 Impurity of lapatinib and salts thereof F.I.S. Fabbrica Italiana Sintetici S.p.A. (IT) 2012-08-22 EP claimed
CN-102321076-A The preparation method of lapatinibditosylate midbody and analogue thereof USTC UNIV SCIENCE TECH CN 2012-01-18 CN claimed
EP-2305634-A1 THE NEW PREPARATION OF ALIPHATIC AMINES WITH SULPHONYL GROUP AND THEIR SALTS Knowa Pharmaceutical (Shanghai) Co. Ltd. (CN) 2011-04-06 EP claimed
US-7683067-B2 3-heterocyclyl-indole derivatives as inhibitors of glycogen synthase kinase-3 (GSK-3) ASTRAZENECA AB (SE) 2010-03-23 US claimed
US-20080275041-A1 3-Heterocyclyl-Indole Derivatives as Inhibitors of Glycogen Synthase Kinase-3 (Gsk-3) ASTRAZENECA AB (SE) 2008-11-06 US claimed
CN-1886397-A 3-heterocyclyl-indole derivatives as inhibitors of glycogen synthase kinase-3 (gsk-3) ASTRAZENECA AB (SE) 2006-12-27 CN claimed
EP-1667990-A2 NEW COMPOUNDS AstraZeneca AB (SE) 2006-06-14 EP claimed
WO-2005027823-A2 3-HETEROCYCLYL-INDOLE DERIVATIVES AS INHIBITORS OF GLYCOGEN SYNTHASE KINASE-3 (GSK-3) ASTRAZENECA AB (SE) 2005-03-31 WO claimed