Hydrochloric Acid

Hydrochloric Acid

SCHEMBL134418

CCOC(=O)CC[C@H](N)C(=O)OCC.Cl

nearest known ligand 0.51

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
GAA known ✓ P10253 2/20 0.43
PTGS2 known ✓ P35354 1/20 0.36
PDE4D known ✓ Q08499 1/20 0.36
L3MBTL1 Q9Y468 2/20 0.51
KMT2A Q03164 2/20 0.49
POLB P06746 1/20 0.49
CYP1A2 P05177 1/20 0.48
MGAM O43451 1/20 0.43
SI P14410 1/20 0.43
MGAM2 Q2M2H8 1/20 0.43
ALDH1A1 P00352 4/20 0.40
TRPA1 O75762 1/20 0.40
NOD1 Q9Y239 2/20 0.39
KDM4E B2RXH2 1/20 0.39
HPGD P15428 1/20 0.39
HSD17B10 Q99714 1/20 0.39
ALOX15 P16050 1/20 0.38
CYP2D6 P10635 1/20 0.38
CYP2C9 P11712 1/20 0.38
CYP2C19 P33261 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 SCHEMBL2012219 1.00 L3MBTL1 (0.51) L3MBTL1KMT2APOLBCYP1A2GAA
Hydrochloric Acid SCHEMBL134419 1.00 L3MBTL1 (0.51) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL207116 0.98 L3MBTL1 (0.53) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL573710 0.98 L3MBTL1 (0.53) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL374738 0.98 L3MBTL1 (0.53) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL20270768 0.96 L3MBTL1 (0.51) L3MBTL1KMT2APOLBCYP1A2GAA
Hydrochloric Acid SCHEMBL6845675 0.94 L3MBTL1 (0.50) L3MBTL1KMT2APOLBCYP1A2GAA
Ethyne SCHEMBL28180627 0.94 L3MBTL1 (0.50) L3MBTL1KMT2APOLBCYP1A2GAA
Acetic Acid SCHEMBL28340742 0.92 L3MBTL1 (0.49) L3MBTL1KMT2APOLBCYP1A2GAA
Ethyne SCHEMBL28279649 0.92 L3MBTL1 (0.49) L3MBTL1KMT2APOLBCYP1A2GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116253682-B Photochromic chiral supermolecular hydrogel and preparation method thereof 中国科学院化学研究所 2025-01-24 CN claimed
CN-119214248-A Pig feed for increasing intramuscular fat of pork and preparation method thereof 中国科学院亚热带农业生态研究所 2024-12-31 CN claimed
CN-119125333-A Separation detection method for related impurities of diethyl L-glutamate hydrochloride 重庆药友制药有限责任公司 2024-12-13 CN claimed
CN-118619955-A Preparation method and application of pemetrexed key intermediate 江苏海洋大学 2024-09-10 CN claimed
CN-118286135-A Skin repair composition and application thereof in cosmetics 上海枫萃生物科技有限公司 2024-07-05 CN claimed
CN-117623969-A Synthesis method of diethyl p-methylamino benzoyl glutamate 南京远淑医药科技有限公司 2024-03-01 CN claimed
CN-117342529-A Hydrogen peroxide gel containing amphiphilic Bola molecule and preparation method thereof 国家纳米科学中心 2024-01-05 CN claimed
CN-116768901-A Preparation method of pemetrexed disodium 贵州阜康仁制药有限公司 2023-09-19 CN claimed
CN-115504897-A Synthetic method of methotrexate intermediate 南京卡文迪许生物工程技术有限公司 2022-12-23 CN claimed
CN-112442038-B Industrial preparation method of pemetrexed disodium 德州德药制药有限公司 2022-09-02 CN claimed
CN-111333658-A Preparation method of pemetrexed disodium hydrate 贵州联科中贝制药科技有限公司 2020-06-26 CN claimed
CN-110749692-A Separation and detection method of L-glutamic acid diethyl ester hydrochloride and optical isomer thereof 扬子江药业集团有限公司 2020-02-04 CN claimed
CN-109734698-A A kind of synthesis technology of Raltitrexed key intermediate 宏冠生物药业有限公司 2019-05-10 CN claimed
EP-2882753-B1 PROCESS FOR THE PREPARATION OF PEMETREXED AND LYSIN SALT THEREOF BERLIN CHEMIE AG (DE) 2016-10-05 EP claimed
US-20160214987-A1 METHOD FOR PREPARING AN INTERMEDIATE FOR PRODUCING HIGH-PURITY PEMETREXED AND METHOD FOR PRODUCING HIGH-PURITY PEMETREXED USING THE INTERMEDIATE SAMYANG BIOPHARMACEUTICALS CORPORATION (KR) 2016-07-28 US claimed
EP-3042904-A1 METHOD FOR PREPARING IMPROVED INTERMEDIATE FOR PRODUCING HIGH-PURITY PEMETREXED AND METHOD FOR PRODUCING HIGH-PURITY PEMETREXED USING INTERMEDIATE Samyang Biopharmaceuticals Corporation (KR) 2016-07-13 EP claimed
EP-2882753-A1 PROCESS FOR THE PREPARATION OF PEMETREXED AND LYSIN SALT THEREOF BERLIN-CHEMIE AG (DE) 2015-06-17 EP claimed
WO-2014024164-A1 PROCESS FOR THE PREPARATION OF PEMETREXED AND LYSIN SALT THEREOF BERLIN-CHEMIE AG (DE) 2014-02-13 WO claimed
CN-1219811-C Protein finishing agent with long tail of methoxy carbowax as well as preparation method and application INST PROCESS ENG CAS (CN) 2005-09-21 CN claimed
CN-1519266-A Protein finishing agent with long tail of methoxy carbowax as well as preparation method and application 中国科学院过程工程研究所 2004-08-11 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-20160214987-A1 METHOD FOR PREPARING AN INTERMEDIATE FOR PRODUCING HIGH-PURITY PEMETREXED AND METHOD FOR PRODUCING HIGH-PURITY PEMETREXED USING THE INTERMEDIATE SAMHD1, IMPDH1, DCTD GAA 2697/4885PTGS2 3002/4885PDE4D 2415/4885

“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.