Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7304854

CC(C)(C)OC(=O)N[C@@H](CCCNC(=N)N)C(=O)O.Cl.O

nearest known ligand 0.52

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 18)

geneUniProtsupporting neighboursconfidence
GAA known ✓ P10253 1/20 0.52
PPARG known ✓ P37231 1/20 0.40
ITGB3 known ✓ P05106 3/20 0.40
ITGA2B known ✓ P08514 3/20 0.40
MAOA known ✓ P21397 1/20 0.40
MAOB known ✓ P27338 1/20 0.40
MEN1 O00255 1/20 0.52
KMT2A Q03164 1/20 0.52
CTSK P43235 10/20 0.49
CTSS P25774 7/20 0.49
CAPN1 P07384 1/20 0.43
CTSL P07711 1/20 0.42
CTSB P07858 1/20 0.42
ALDH1A1 P00352 1/20 0.42
TSHR P16473 1/20 0.42
PPARA Q07869 1/20 0.40
JAK3 P52333 1/20 0.39
BTK Q06187 1/20 0.39

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 SCHEMBL10723070 1.00 MEN1 (0.52) MEN1GAAKMT2ACTSKCTSS
Hydrochloric Acid SCHEMBL10932432 1.00 MEN1 (0.52) MEN1GAAKMT2ACTSKCTSS
Hydrochloric Acid SCHEMBL10444447 0.99 MEN1 (0.54) MEN1GAAKMT2ACTSKCTSS
Water SCHEMBL10332189 0.99 MEN1 (0.54) MEN1GAAKMT2ACTSKCTSS
Hydrochloric Acid SCHEMBL8630295 0.99 MEN1 (0.54) MEN1GAAKMT2ACTSKCTSS
Hydrochloric Acid SCHEMBL7264801 0.99 MEN1 (0.54) MEN1GAAKMT2ACTSKCTSS
Water SCHEMBL10332190 0.99 MEN1 (0.54) MEN1GAAKMT2ACTSKCTSS
SCHEMBL2367531 0.97 MEN1 (0.55) MEN1GAAKMT2ACTSKCTSS
SCHEMBL7364210 0.97 MEN1 (0.55) MEN1GAAKMT2ACTSKCTSS
SCHEMBL1486276 0.97 MEN1 (0.55) MEN1GAAKMT2ACTSKCTSS

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108864006-A N- tertbutyloxycarbonyl-N '-(Pentamethyl Dihydrobenzofuranes -5- sulfonyl)-L-arginine synthetic method 上海吉奉生物科技有限公司 2018-11-23 CN claimed
JP-60166657-A None JP disclosed
CN-113698457-B Preparation method of gonadorelin acetate 上海丽珠制药有限公司 2024-06-11 CN disclosed
CN-116829949-A Compositions for detecting or measuring analytes 伯蒂斯有限公司 2023-09-29 CN disclosed
WO-2023075435-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE 주식회사 베르티스 2023-05-04 WO disclosed
US-20220283131-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTES BERTIS CO., LTD. (KR) 2022-09-08 US disclosed
CN-108864006-A N- tertbutyloxycarbonyl-N '-(Pentamethyl Dihydrobenzofuranes -5- sulfonyl)-L-arginine synthetic method 上海吉奉生物科技有限公司 2018-11-23 CN disclosed
CN-108864006-A N- tertbutyloxycarbonyl-N '-(Pentamethyl Dihydrobenzofuranes -5- sulfonyl)-L-arginine synthetic method 上海吉奉生物科技有限公司 2018-11-23 CN disclosed
EP-0526877-A2 Peptide aldehydes as antithrombotic agents Bristol-Myers Squibb Company (US) 1993-02-10 EP disclosed
EP-0152872-B1 ARGINYL-3-CARBOXY-4-HYDROXYANILIDE AND THEIR USE NITTO BOSEKI CO., LTD. (JP) 1988-05-04 EP disclosed
US-4703036-A ANTICOAGULANTS RICHTER GEDEON VEGYESZETI GYAR RT (HU) 1987-10-27 US disclosed
JP-S60166657-A ARGINYL-3-CARBOXY-4-HYDROXYANILIDE NITTO BOSEKI CO LTD 1985-08-29 JP disclosed
EP-0152872-A1 Arginyl-3-carboxy-4-hydroxyanilide and their use NITTO BOSEKI CO., LTD. (JP) 1985-08-28 EP disclosed
US-4316889-A ANTICOAGULANTS RICHTER GEDEON VEGYESZETI GYAR RT. (HU) 1982-02-23 US disclosed