Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3017606

Cl.NC(CCC(=O)O)c1ccccc1

nearest known ligand 0.48

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
GABRP known ✓ O00591 2/20 0.43
GABRD known ✓ O14764 2/20 0.43
GABRA1 known ✓ P14867 2/20 0.43
GABRB1 known ✓ P18505 2/20 0.43
GABRG2 known ✓ P18507 2/20 0.43
GABRB3 known ✓ P28472 2/20 0.43
GABRA5 known ✓ P31644 2/20 0.43
GABRA3 known ✓ P34903 2/20 0.43
GABRA2 known ✓ P47869 2/20 0.43
GABRB2 known ✓ P47870 2/20 0.43
GABRA4 known ✓ P48169 2/20 0.43
GABRE known ✓ P78334 2/20 0.43
GABRA6 known ✓ Q16445 2/20 0.43
GABRG1 known ✓ Q8N1C3 2/20 0.43
GABRG3 known ✓ Q99928 2/20 0.43
GABRQ known ✓ Q9UN88 2/20 0.43
GRIN2D known ✓ O15399 1/20 0.43
GRIN3B known ✓ O60391 1/20 0.43
GRIN1 known ✓ Q05586 1/20 0.43
GRIN2A known ✓ Q12879 1/20 0.43

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
SCHEMBL288399 0.98 CYP1A2 (0.48) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL372488 0.98 CYP1A2 (0.48) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL12682235 0.98 CYP1A2 (0.48) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL27477537 0.86 LTA4H (0.49) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL10356118 0.86 LTA4H (0.49) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL671557 0.86 LTA4H (0.49) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL11115553 0.86 SCN4A (0.42) CYP2D6GABBR2GABBR1GRM2GRM3
SCHEMBL21099020 0.85 TBXAS1 (0.53) CYP1A2ALDH1A1CYP2D6TSHRCYP2C19
SCHEMBL29263658 0.84 CYP1A2 (0.47) CYP1A2CYP2D6CYP2C19MAPK1
SCHEMBL16015375 0.82 ALDH1A1 (0.47) ALDH1A1SLC15A1GRM2GRM3SCN4A

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
US-20190298676-A1 COMPOSITIONS AND METHODS FOR PROVIDING SUSTAINED NATURAL SLEEP FarmaKeio Nutraceuticals, LLC (US) 2019-10-03 US claimed
US-20190106378-A1 ANTIMICROBIALS FOR PRESERVATION OF HOME AND PERSONAL CARE PRODUCTS GALAXY SURFACTANTS LTD. 2019-04-11 US claimed
US-20220110896-A1 COMPOSITIONS AND METHODS FOR PROVIDING SUSTAINED NATURAL SLEEP FarmaKeio Nutraceuticals, LLC (US) 2022-04-14 US disclosed
WO-2020141734-A1 METHOD FOR PREPARING CHIRAL GAMMA-LACTAM COMPOUND AND METAL COMPLEX THEREFOR 기초과학연구원 2020-07-09 WO disclosed
US-20190298676-A1 COMPOSITIONS AND METHODS FOR PROVIDING SUSTAINED NATURAL SLEEP FarmaKeio Nutraceuticals, LLC (US) 2019-10-03 US disclosed
CN-103232356-A Technology for preparing 3-phenyl-4-aminobutyric acid hydrochloride TIANJIN JUDE TECHNOLOGY CO LTD 2013-08-07 CN disclosed
CN-101684071-B Method for splitting DL-p-hydroxymandelic acid SHANGHAI BAOSTEEL CHEMICAL CO 2012-12-26 CN disclosed
US-20100203059-A1 METHOD OF TREATING A PATHOLOGICAL SYNDROME AND A PHARMACEUTICAL AGENT OLEG ILIICH EPSHTEIN (RU) 2010-08-12 US disclosed
US-5387671-A Antiinflammatory agents ABBOTT LABORATORIES (US) 1995-02-07 US disclosed
EP-0564533-A4 MODIFIED HEXA- AND HEPTAPEPTIDE ANAPHYLATOXIN RECEPTOR LIGANDS ABBOTT LAB (US) 1994-11-02 EP disclosed
EP-0564533-A1 MODIFIED PENTA- AND HEXAPEPTIDE ANAPHYLATOXIN RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 1993-10-13 EP disclosed
WO-1992012168-A1 MODIFIED HEXA- AND HEPTAPEPTIDE ANAPHYLATOXIN RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 1992-07-23 WO disclosed
US-4683238-A 2,3,4,9-tetrahydro beta carboline derivatives, useful as antihypertensive agents BOEHRINGER INGELHEIM KG (DE) 1987-07-28 US 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-20220110896-A1 COMPOSITIONS AND METHODS FOR PROVIDING SUSTAINED NATURAL SLEEP CHAT, PER2, CRY2 GABRP 920/4885GABRD 2008/4885GABRA1 677/4885
US-20190298676-A1 COMPOSITIONS AND METHODS FOR PROVIDING SUSTAINED NATURAL SLEEP CHAT, PER2, CRY2 GABRP 920/4885GABRD 2008/4885GABRA1 677/4885
US-20190106378-A1 ANTIMICROBIALS FOR PRESERVATION OF HOME AND PERSONAL CARE PRODUCTS C9, CFH, CFB GABRP 2391/4885GABRD 3643/4885GABRA1 3447/4885

“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.