Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1643496

CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2F)c(C)n(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1.Cl

nearest known ligand 0.90

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 9)

geneUniProtsupporting neighboursconfidence
GNRHR known ✓ P30968 20/20 0.90
ADRB2 known ✓ P07550 1/20 0.83
OPRK1 known ✓ P41145 1/20 0.83
CYP3A4 P08684 14/20 0.90
APLNR P35414 1/20 0.83
GLP1R P43220 1/20 0.83
CX3CR1 P49238 1/20 0.83
FFAR4 Q5NUL3 1/20 0.83
GPR119 Q8TDV5 1/20 0.83

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 SCHEMBL29960614 1.00 GNRHR (0.90) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL1642456 0.99 GNRHR (0.91) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL5762499 0.99 GNRHR (0.91) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL19549442 0.99 GNRHR (0.91) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL29722073 0.99 GNRHR (0.91) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL25445039 0.93 GNRHR (0.81) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL1644181 0.93 GNRHR (0.80) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL19549541 0.93 GNRHR (0.80) GNRHRCYP3A4ADRB2APLNROPRK1
SCHEMBL26007655 0.93 GNRHR (0.91) GNRHRCYP3A4ADRB2APLNROPRK1
Elagolix SCHEMBL1642523 0.93 GNRHR (1.00) GNRHRCYP3A4ADRB2APLNROPRK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200255387-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES NEUROCRINE BIOSCIENCES, INC. 2020-08-13 US disclosed
US-20190218191-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES NEUROCRINE BIOSCIENCES, INC. 2019-07-18 US disclosed
US-20180346428-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES NEUROCRINE BIOSCIENCES, INC. 2018-12-06 US disclosed
US-9868706-B2 Processes for the preparation of uracil derivatives NEUROCRINE BIOSCIENCES, INC. (US) 2018-01-16 US disclosed
US-20170320836-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES NEUROCRINE BIOSCIENCES, INC. 2017-11-09 US disclosed
US-9382214-B2 Processes for the preparation of uracil derivatives Neurocine Biosciences, Inc. (US) 2016-07-05 US disclosed
US-8765948-B2 Processes for the preparation of uracil derivatives NEUROCRINE BIOSCIENCES, INC. (US) 2014-07-01 US disclosed
US-20110098472-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES NEUROCRINE BIOSCIENCES, INC. 2011-04-28 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 (5 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-20200255387-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES GNRHR, FSHR, GHRHR GNRHR 1/4885ADRB2 1892/4885OPRK1 481/4885
US-20190218191-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES GNRHR, FSHR, GHRHR GNRHR 1/4885ADRB2 1892/4885OPRK1 481/4885
US-20180346428-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES GNRHR, FSHR, GHRHR GNRHR 1/4885ADRB2 1892/4885OPRK1 481/4885
US-20110098472-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES GNRHR, FSHR, GHRHR GNRHR 1/4885ADRB2 1892/4885OPRK1 481/4885
US-20170320836-A1 PROCESSES FOR THE PREPARATION OF URACIL DERIVATIVES GNRHR, FSHR, GHRHR GNRHR 1/4885ADRB2 1892/4885OPRK1 481/4885

“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.