Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2634079

Cl.Cl.NCCNC(=O)c1nc(N)c(C(=O)NCCN)nc1N

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
MAOB known ✓ P27338 3/20 0.42
KCNA4 known ✓ P22459 1/20 0.33
KCNA1 known ✓ Q09470 1/20 0.33
KMT2A Q03164 3/20 0.44
PMP22 Q01453 2/20 0.44
MEN1 O00255 1/20 0.44
BLM P54132 1/20 0.44
KDM4E B2RXH2 3/20 0.43
ALDH1A1 P00352 1/20 0.43
HSD17B10 Q99714 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
CYP1A2 P05177 2/20 0.42
TSHR P16473 1/20 0.42
NFKB1 P19838 1/20 0.42
LMNA P02545 1/20 0.39
TERT O14746 2/20 0.38
CHEK1 O14757 1/20 0.38
CHEK2 O96017 1/20 0.38
CYP3A4 P08684 1/20 0.37
THPO P40225 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
SCHEMBL2634478 0.98 KDM4E (0.44) KMT2APMP22MEN1BLMKDM4E
SCHEMBL16748713 0.89 GABRG2 (0.41) KMT2APMP22MEN1BLMKDM4E
Trifluoroacetic Acid SCHEMBL30286292 0.88 CSNK1D (0.43) KMT2APMP22MEN1BLMKDM4E
SCHEMBL9608994 0.86 KDM4E (0.43) KMT2AMEN1KDM4EALDH1A1HSD17B10
SCHEMBL1429031 0.84 SCNN1A (0.50) KMT2APMP22MEN1BLMKDM4E
Hydrochloric Acid SCHEMBL2634029 0.80 HPGD (0.38) KDM4EALDH1A1HSD17B10L3MBTL1TSHR
SCHEMBL15185777 0.80 KDM4E (0.43) KMT2AKDM4EALDH1A1HSD17B10L3MBTL1
SCHEMBL18230698 0.78 CA1 (0.42) KDM4EALDH1A1HSD17B10L3MBTL1LMNA
SCHEMBL12184961 0.78 HPGD (0.38) KDM4EALDH1A1HSD17B10L3MBTL1TSHR
SCHEMBL12997160 0.77 SMN1; SMN2 (0.41) KMT2AMEN1KDM4EALDH1A1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190302026-A1 Uniform, Functionalized, Cross-Linked Nanostructures for Monitoring pH WOOLEY KAREN L (US) 2019-10-03 US disclosed
US-20180335385-A1 Uniform, Functionalized, Cross-Linked Nanostructures for Monitoring pH THE WASHINGTON UNIVERSITY 2018-11-22 US disclosed
US-9662387-B2 Functional, cross-linked nanostructures for tandem optical imaging and therapy MALLINCKRODT LLC (US) 2017-05-30 US disclosed
US-20160256550-A1 FUNCTIONAL, CROSS-LINKED NANOSTRUCTURES FOR TANDEM OPTICAL IMAGING AND THERAPY MALLINCKRODT LLC (US) 2016-09-08 US disclosed
US-9295650-B2 Functional, cross-linked nanostructures for tandem optical imaging and therapy MALLINCKRODT LLC (US) 2016-03-29 US disclosed
US-20150346099-A1 Uniform, Functionalized, Cross-Linked Nanostructures for Monitoring pH WOOLEY KAREN L (US) 2015-12-03 US disclosed
US-20130210156-A1 Uniform, Functionalized, Cross-Linked Nanostructures for Monitoring pH THE TEXAS A&M UNIVERSITY SYSTEM 2013-08-15 US disclosed
US-20130137976-A1 Functional, Cross-Linked Nanostructures for Tandem Optical Imaging and Therapy IKARIA THERAPEUTICS LLC 2013-05-30 US disclosed
EP-2571529-A2 FUNCTIONAL, CROSS-LINKED NANOSTRUCTURES FOR TANDEM OPTICAL IMAGING AND THERAPY Mallinckrodt LLC (US) 2013-03-27 EP disclosed
WO-2011143540-A1 UNIFORM, FUNCTIONALIZED, CROSS-LINKED NANOSTRUCTURES FOR MONITORING pH MALLINCKRODT LLC (US) 2011-11-17 WO disclosed
WO-2011143524-A2 FUNCTIONAL, CROSS-LINKED NANOSTRUCTURES FOR TANDEM OPTICAL IMAGING AND THERAPY MALLINCKRODT LLC (US) 2011-11-17 WO disclosed
US-20100311903-A1 Photonic Shell-Core Cross Linked and Functionalized Nanostructures for Biological Applications MALLINCKRODT LLC 2010-12-09 US disclosed
EP-2217281-A2 PHOTONIC SHELL-CORE CROSS LINKED AND FUNCTIONALIZED NANOSTRUCTURES FOR BIOLOGICAL APPLICATIONS Mallinckrodt Inc. (US) 2010-08-18 EP disclosed
WO-2009061473-A2 PHOTONIC SHELL-CORE CROSS LINKED AND FUNCTIONALIZED NANOSTRUCTURES FOR BIOLOGICAL APPLICATIONS MALLINCKRODT INC. (US) 2009-05-14 WO 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 (4 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-20160256550-A1 FUNCTIONAL, CROSS-LINKED NANOSTRUCTURES FOR TANDEM OPTICAL IMAGING AND THERAPY MTCL3, EPHA2, UACA MAOB 1895/4885KCNA4 3413/4885KCNA1 3617/4885
US-20190302026-A1 Uniform, Functionalized, Cross-Linked Nanostructures for Monitoring pH MUC1, CD44, PFN1 MAOB 3976/4885KCNA4 4203/4885KCNA1 3662/4885
US-20130137976-A1 Functional, Cross-Linked Nanostructures for Tandem Optical Imaging and Therapy MTCL3, EPHA2, UACA MAOB 1895/4885KCNA4 3413/4885KCNA1 3617/4885
US-20180335385-A1 Uniform, Functionalized, Cross-Linked Nanostructures for Monitoring pH MUC1, CD44, PFN1 MAOB 3976/4885KCNA4 4203/4885KCNA1 3662/4885

“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.