Hydrochloric Acid

Hydrochloric Acid

SCHEMBL624145

COC(=O)CC[C@H](N)C(=O)OC.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
CA2 known ✓ P00918 1/20 0.38
GRIN2D known ✓ O15399 1/20 0.35
GRIN3B known ✓ O60391 1/20 0.35
GRIN1 known ✓ Q05586 1/20 0.35
GRIN2A known ✓ Q12879 1/20 0.35
GRIN2B known ✓ Q13224 1/20 0.35
GRIN2C known ✓ Q14957 1/20 0.35
GRIN3A known ✓ Q8TCU5 1/20 0.35
GAA known ✓ P10253 1/20 0.34
SLC1A1 P43005 2/20 0.53
TSHR P16473 4/20 0.48
LMNA P02545 2/20 0.45
KDM4E B2RXH2 1/20 0.45
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
LTA4H P09960 3/20 0.41
CA12 O43570 2/20 0.38
CA1 P00915 1/20 0.38
CA9 Q16790 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.37

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 SCHEMBL1238805 1.00 SLC1A1 (0.53) SLC1A1TSHRLMNAKDM4EKMT2A
Hydrochloric Acid SCHEMBL624146 1.00 SLC1A1 (0.53) SLC1A1TSHRLMNAKDM4EKMT2A
SCHEMBL1318285 0.98 SLC1A1 (0.55) SLC1A1TSHRLMNAKDM4EKMT2A
SCHEMBL131050 0.98 SLC1A1 (0.55) SLC1A1TSHRLMNAKDM4EKMT2A
SCHEMBL131049 0.98 SLC1A1 (0.55) SLC1A1TSHRLMNAKDM4EKMT2A
SCHEMBL28180863 0.96 SLC1A1 (0.53) SLC1A1TSHRLMNAKDM4EKMT2A
SCHEMBL20474981 0.89 SLC1A1 (0.47) SLC1A1TSHRLMNAKDM4EKMT2A
SCHEMBL10633361 0.89 SLC1A1 (0.47) SLC1A1TSHRLMNAKDM4EKMT2A
Hydrochloric Acid SCHEMBL7163088 0.88 TSHR (0.52) SLC1A1TSHRLMNAKDM4EKMT2A
Hydrochloric Acid SCHEMBL28514709 0.88 TSHR (0.52) SLC1A1TSHRLMNAKDM4EKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119409588-A Caffeoyl amino acid methyl ester derivative and preparation method and application thereof 西北大学 2025-02-11 CN claimed
CN-119351754-A Recycling treatment method of copper-containing sludge 江西省金瑞环保科技有限公司 2025-01-24 CN claimed
CN-119241617-A 2 '-Deoxy-2' -fluoro-N4-substituted cytidine compound, preparation method and application thereof 河南省科学院高新技术研究中心 2025-01-03 CN claimed
CN-119144151-A Preparation of hydrogels and uses thereof 粤港澳大湾区精准医学研究院(广州) 2024-12-17 CN claimed
CN-117946007-A Curcumin-amino acid methyl ester derivative and preparation method and application thereof 河北科技大学 2024-04-30 CN claimed
CN-117903078-A Amide derivative containing 3, 4-dichloro isothiazole, preparation method and application thereof 南开大学 2024-04-19 CN claimed
CN-113912524-B Polypeptide compound containing sulfur amide and synthesis method thereof 华东师范大学 2023-12-01 CN claimed
CN-115819652-B 2-aminopentanedioxime acid modified polyacrylic acid chelate resin and preparation method and application thereof 中南大学 2023-09-05 CN claimed
CN-115947670-A Synthesis process of N-tert-butyloxycarbonyl-L-glutamic acid dimethyl ester 常州吉恩药业有限公司 2023-04-11 CN claimed
CN-115819652-A 2-amino pentanedioxyhydroxamic acid modified polyacrylic acid chelating resin and preparation method and application thereof 中南大学 2023-03-21 CN claimed
CN-113527399-A Ginsenoside CK derivative and application thereof in preparation of antitumor drugs 陕西巨子生物技术有限公司 2021-10-22 CN claimed
CN-111807994-A L-glutamic acid derivative and synthesis method and application thereof 四川嘉瑛莱科技有限责任公司 2020-10-23 CN claimed
CN-111574973-A Three-water-retention-based drilling fluid system 石家庄华莱鼎盛科技有限公司 2020-08-25 CN claimed
US-20130165654-A1 PROCESSES FOR PREPARING PEMETREXED DR. REDDY'S LABORATORIES, INC. (US) 2013-06-27 US claimed
CN-101928321-B Acidic amino acid chemically-modified ursolic acid derivatives with anti-cancer activities UNIV FUZHOU 2012-09-05 CN claimed
EP-2464650-A2 PROCESSES FOR PREPARING PEMETREXED Dr. Reddy's Laboratories, Ltd. (IN) 2012-06-20 EP claimed
CN-101333173-B N-[4-(butanal-4-group)-benzoyl]-L-glutamic acid dimethyl ester compound and method for preparing pemetrexed by using the compounds QILU PHARMACEUTICAL CO LTD 2011-08-10 CN claimed
WO-2011019986-A2 PROCESSES FOR PREPARING PEMETREXED DR. REDDY'S LABORATORIES LTD. (IN) 2011-02-17 WO claimed
CN-101928321-A Acidic amino acid chemically-modified ursolic acid derivatives with anti-cancer activities UNIV FUZHOU 2010-12-29 CN claimed
CN-101333173-A N-[4-(butanal-4-group)-benzoyl]-L-glutamic acid dimethyl ester compound and method for preparing pemetrexed by using the compounds QILU PHARMACEUTICAL CO LTD (CN) 2008-12-31 CN claimed

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-20130165654-A1 PROCESSES FOR PREPARING PEMETREXED TYMP, TYMS, DPYD CA2 4647/4885GRIN2D 3971/4885GRIN3B 3724/4885

“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.