Hydrochloric Acid

Hydrochloric Acid

SCHEMBL17239121

Cl.N=C(N)NC[C@H](N)C(=O)O

nearest known ligand 0.44

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
PTGS1 known ✓ P23219 1/20 0.39
CASR known ✓ P41180 1/20 0.37
GRIN2D known ✓ O15399 1/20 0.37
GRIN3B known ✓ O60391 1/20 0.37
GRIN1 known ✓ Q05586 1/20 0.37
GRIN2A known ✓ Q12879 1/20 0.37
GRIN2B known ✓ Q13224 1/20 0.37
GRIN2C known ✓ Q14957 1/20 0.37
GRIN3A known ✓ Q8TCU5 1/20 0.37
GFPT1 Q06210 1/20 0.44
GGT1 P19440 4/20 0.42
ALOX15 P16050 1/20 0.40
BLM P54132 1/20 0.40
PMP22 Q01453 1/20 0.40
KMT2A Q03164 1/20 0.40
SLC7A11 Q9UPY5 1/20 0.39
ARG2 P78540 1/20 0.38
NOS3 P29474 1/20 0.38
NOS1 P29475 1/20 0.38
NOS2 P35228 1/20 0.38

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 SCHEMBL503105 1.00 GFPT1 (0.44) GFPT1GGT1ALOX15BLMPMP22
SCHEMBL1527344 0.98 GFPT1 (0.46) GFPT1GGT1ALOX15BLMPMP22
SCHEMBL574087 0.98 GFPT1 (0.46) GFPT1GGT1ALOX15BLMPMP22
SCHEMBL393844 0.98 GFPT1 (0.46) GFPT1GGT1ALOX15BLMPMP22
Adipic Acid SCHEMBL8055763 0.87 BHMT (0.45) GFPT1ALOX15BLMPMP22KMT2A
SCHEMBL19371887 0.82 GFPT1 (0.32) GFPT1
SCHEMBL22122969 0.82 GFPT1 (0.32) GFPT1
SCHEMBL27644223 0.82 SLC7A5 (0.42) GGT1ALOX15BLMPMP22KMT2A
SCHEMBL27644228 0.82 SLC7A5 (0.42) GGT1ALOX15BLMPMP22KMT2A
SCHEMBL5812527 0.80 SLC7A5 (0.41) GGT1ALOX15BLMPMP22KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113354573-A Method for large-scale production of alpha, alpha-terpyridine 河南阿尔法医药科技有限公司 2021-09-07 CN claimed
EP-4401758-A1 FACILITATED DELIVERY OF CONCENTRATED ANTIBODY FORMULATIONS USING HYALURONIDASE Takeda Pharmaceutical Company Limited (JP) 2024-07-24 EP disclosed
CN-114288253-B Stable intranasal carbetocin formulations 阿卡蒂亚药品公司 2024-04-02 CN disclosed
CN-112969450-B Carbetocin pharmaceutical product and process for preparing the same 阿卡蒂亚药品公司 2023-05-30 CN disclosed
WO-2023042096-A1 FACILITATED DELIVERY OF CONCENTRATED ANTIBODY FORMULATIONS USING HYALURONIDASE TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-03-23 WO disclosed
CN-113354573-B Method for large-scale production of alpha, alpha-terpyridine 河南阿尔法医药科技有限公司 2023-03-17 CN disclosed
US-11207373-B2 Agitation process for preparing a carbetocin drug product LEVO THERAPEUTICS, INC. (US) 2021-12-28 US disclosed
CN-113354573-A Method for large-scale production of alpha, alpha-terpyridine 河南阿尔法医药科技有限公司 2021-09-07 CN disclosed
US-20200093885-A1 CARBETOCIN DRUG PRODUCT AND PROCESS FOR PREPARING THE SAME ACADIA PHARMACEUTICALS, INC. 2020-03-26 US disclosed
US-9655902-B2 Guanidine derivatives for the treatment of hepatitis C BRISTOL-MYERS SQUIBB COMPANY (US) 2017-05-23 US disclosed
EP-2948445-B1 GUANIDINE DERIVATIVES FOR THE TREATMENT OF HEPATITIS C BRISTOL MYERS SQUIBB CO (US) 2017-05-17 EP disclosed
US-20150320757-A1 GUANIDINE DERIVATIVES FOR THE TREATMENT OF HEPATITIS C BRISTOL-MYERS SQUIBB COMPANY 2015-11-12 US disclosed
CN-104936952-A Guanidine derivatives for the treatment of hepatitis c BRISTOL MYERS SQUIBB CO 2015-09-23 CN 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 (3 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-11207373-B2 Agitation process for preparing a carbetocin drug product PRKD2, PRKD1, DCTD PTGS1 4722/4885CASR 4869/4885GRIN2D 1353/4885
US-20200093885-A1 CARBETOCIN DRUG PRODUCT AND PROCESS FOR PREPARING THE SAME PRKD2, DCTD, NCAPD2 PTGS1 4664/4885CASR 4877/4885GRIN2D 2267/4885
US-20150320757-A1 GUANIDINE DERIVATIVES FOR THE TREATMENT OF HEPATITIS C GMPS, GANC, GUCY1A1 PTGS1 483/4885CASR 4855/4885GRIN2D 4614/4885

“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.