Hydrochloric Acid

Hydrochloric Acid

SCHEMBL715023

Cl.NCC(=O)NCC(=O)OCc1ccccc1

nearest known ligand 0.56

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
GLA known ✓ P06280 1/20 0.49
NR3C1 known ✓ P04150 1/20 0.48
OPRK1 known ✓ P41145 1/20 0.48
L3MBTL1 Q9Y468 2/20 0.53
ALDH1A1 P00352 1/20 0.53
MAPK1 P28482 1/20 0.53
MEN1 O00255 4/20 0.50
KMT2A Q03164 4/20 0.50
LMNA P02545 1/20 0.49
AOC3 Q16853 1/20 0.49
LTA4H P09960 1/20 0.49
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2D6 P10635 1/20 0.48
CYP2C9 P11712 1/20 0.48
CYP2C19 P33261 1/20 0.48
ABCC3 O15438 1/20 0.48
NR1I2 O75469 1/20 0.48
ABCB11 O95342 1/20 0.48
RARG P13631 1/20 0.48

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
SCHEMBL5538472 0.98 L3MBTL1 (0.54) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
Hydrochloric Acid SCHEMBL8181153 0.97 L3MBTL1 (0.50) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
Hydrochloric Acid SCHEMBL25310405 0.97 L3MBTL1 (0.50) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
SCHEMBL26287992 0.95 L3MBTL1 (0.51) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
Trifluoroacetic Acid SCHEMBL7758264 0.91 MEN1 (0.49) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
SCHEMBL25681603 0.84 ALDH1A1 (0.56) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
SCHEMBL29375726 0.83 LTA4H (0.48) L3MBTL1ALDH1A1MAPK1KMT2ALMNA
Hydrochloric Acid SCHEMBL11684413 0.83 ALDH1A1 (0.51) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
SCHEMBL23518457 0.83 ALDH1A1 (0.51) L3MBTL1ALDH1A1MAPK1MEN1KMT2A
SCHEMBL4447797 0.83 LMNA (0.54) ALDH1A1MEN1KMT2ALMNACYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-11343296-A None JP disclosed
EP-2967801-B1 INJECTABLE BIODEGRADABLE BONE MATRIX FOR MULTIPLE MYELOMA LESION AUGMENTATION AND OSTEOPOROSIS UNIV TOLEDO (US) 2020-07-08 EP disclosed
US-20160030631-A1 Injectable Biodegradable Bone Matrix for Multiple Myeloma Lesion Augmentation and Osteoporosis THE UNIVERSITY OF TOLEDO (US) 2016-02-04 US disclosed
EP-2967801-A2 INJECTABLE BIODEGRADABLE BONE MATRIX FOR MULTIPLE MYELOMA LESION AUGMENTATION AND OSTEOPOROSIS The University of Toledo (US) 2016-01-20 EP disclosed
CN-105263438-A Injectable biodegradable bone matrix for multiple myeloma lesion augmentation and osteoporosis UNIV TOLEDO 2016-01-20 CN disclosed
EP-1894890-B1 TRANSITION METAL OXIDE NANO-TUBE JAPAN SCIENCE & TECH AGENCY (JP) 2014-10-22 EP disclosed
WO-2014160232-A2 INJECTABLE BIODEGRADABLE BONE MATRIX FOR MULTIPLE MYELOMA LESION AUGMENTATION AND OSTEOPOROSIS THE UNIVERSITY OF TOLEDO (US) 2014-10-02 WO disclosed
US-8586638-B2 Parakeratosis inhibitor and skin preparation for external use SHISEIDO COMPANY, LTD (JP) 2013-11-19 US disclosed
CN-102274130-B Application of n- benzene sulfonyl-l-glutamic acid or saline thereof SHISEIDO CO LTD 2013-06-12 CN disclosed
US-20120253064-A1 PARAKERATOSIS INHIBITOR AND SKIN PREPARATION FOR EXTERNAL USE SHISEIDO COMPANY, LTD. (JP) 2012-10-04 US disclosed
EP-1894890-A1 TRANSITION METAL OXIDE NANO-TUBE Japan Science and Technology Agency (JP) 2008-03-05 EP disclosed
US-20070292338-A1 Transition Metal Oxide Nano-Tube JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2007-12-20 US disclosed
US-20070225380-A1 Parakeratosis Inhibitor and Skin Preparation for External use SHISEIDO COMPANY LTD. (JP) 2007-09-27 US disclosed
CN-1886114-A Parakeratosis inhibitor and composition for external use on skin SHISEIDO CO LTD (JP) 2006-12-27 CN disclosed
EP-1688126-A1 PARAKERATOSIS INHIBITOR AND EXTERNAL COMPOSITION FOR SKIN SHISEIDO COMPANY LIMITED (JP) 2006-08-09 EP disclosed
US-6030640-A Oligoglycine compound, fibrous microtube of oligoglycine compound and process of producing fibrous microtube DIRECTOR-GENERAL OF AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2000-02-29 US disclosed
JP-H11343296-A DOUBLE-HEADED LIPID CONTAINING C END OF OLIGOPEPTIDE CHAIN AGENCY OF IND SCIENCE & TECHNOL 1999-12-14 JP disclosed
US-5910565-A PEPTIDE LIPID WHICH WILL FORM MOLECULAR ASSEMBLIES (WHICH ARE STABLE IN A DRIED STATE) WHEN ALLOWED TO STAND FOR TWO TO THREE WEEKS IN AN AQUEOUS SOLUTION DIRECTOR-GENERAL OF AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 1999-06-08 US disclosed
US-5876748-A DRUG DELIVERY DIRECTOR-GENERAL OF AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 1999-03-02 US disclosed
US-4092304-A OLIGOPEPTIDE; ANALGESICS, ANTIDIARRHEAL AGENTS, NON-ADDICTING NARCOTIC ANTAGONISTS G. D. SEARLE & CO. (US) 1978-05-30 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-20160030631-A1 Injectable Biodegradable Bone Matrix for Multiple Myeloma Lesion Augmentation and Osteoporosis SOST, COL2A1, COL1A1 GLA 39/4885NR3C1 2789/4885OPRK1 2731/4885
US-20120253064-A1 PARAKERATOSIS INHIBITOR AND SKIN PREPARATION FOR EXTERNAL USE CUTA, HPN, PRSS1 GLA 53/4885NR3C1 4602/4885OPRK1 4617/4885
US-20070225380-A1 Parakeratosis Inhibitor and Skin Preparation for External use CUTA, HPN, DNPEP GLA 164/4885NR3C1 4791/4885OPRK1 4322/4885

“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.