Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5757732

CC(C)(C)c1cnc(C[S+]=C(N)N)o1.Cl

nearest known ligand 0.41

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 16)

geneUniProtsupporting neighboursconfidence
CDK4 known ✓ P11802 8/20 0.38
KDR known ✓ P35968 1/20 0.35
CDK2 P24941 20/20 0.41
CCNE2 O96020 13/20 0.38
CCNE1 P24864 13/20 0.38
CDK1 P06493 10/20 0.38
CCNB1 P14635 10/20 0.38
CCNB2 O95067 9/20 0.38
CCNB3 Q8WWL7 9/20 0.38
CCND1 P24385 8/20 0.38
CCND2 P30279 6/20 0.38
CCND3 P30281 6/20 0.38
CDK9 P50750 2/20 0.33
CCNT1 O60563 1/20 0.33
CDK7 P50613 1/20 0.33
CCNH P51946 1/20 0.33

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
SCHEMBL17328441 0.72 CDK2 (0.43) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL5724749 0.72 CDK2 (0.45) CDK2CCNE2CCNE1CDK1CCNB1
Hydrochloric Acid SCHEMBL3710324 0.72 CDK2 (0.45) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL10268216 0.70 CDK2 (0.46) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL29285026 0.69 CDK2 (0.43) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL6224593 0.69 CDK2 (0.50) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL12142296 0.69 CDK2 (0.45) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL3468710 0.69 CDK2 (0.45) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL18613960 0.69 CDK2 (0.45) CDK2CCNE2CCNE1CDK1CCNB1
SCHEMBL13827907 0.67 CDK2 (0.44) CDK2CCNE2CCNE1CDK1CCNB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6897321-B2 Process for preparing azacycloalkanoylaminothiazoles (LD 137e) BRISTON MYERS SQUIBB COMPANY (US) 2005-05-24 US claimed
US-20040063767-A1 Process for preparing azacycloalkanoylaminothiazoles (LD 137e) CHEN BANG-CHI (US) 2004-04-01 US claimed
US-20020099217-A1 Process for preparing azacycloalkanoylaminothiazoles CHEN BANG-CHI (US) 2002-07-25 US claimed
US-20010006976-A1 Process for preparing azacycloalkanoylaminothiazoles BRISTOL-MYERS SQUIBB COMPANY 2001-07-05 US claimed
EP-1303514-B9 PROCESS FOR PREPARING AZACYCLOALKANOYLAMINOTHIAZOLES BRISTOL MYERS SQUIBB CO (US) 2006-11-08 EP disclosed
EP-1303514-B1 PROCESS FOR PREPARING AZACYCLOALKANOYLAMINOTHIAZOLES BRISTOL MYERS SQUIBB CO (US) 2005-07-20 EP disclosed
US-6897321-B2 Process for preparing azacycloalkanoylaminothiazoles (LD 137e) BRISTON MYERS SQUIBB COMPANY (US) 2005-05-24 US disclosed
US-20040063767-A1 Process for preparing azacycloalkanoylaminothiazoles (LD 137e) CHEN BANG-CHI (US) 2004-04-01 US disclosed
US-6639074-B2 Reacting an alpha -substituted ketone with a cyclic alkylenetetramine in solvent(s) to form a quaternary ammonium salt; reacting with acid in solvent(s) form an alpha -amino ketone; reacting with acyl derivative; dehydrating BRISTOL MYERS SQUIBB COMPANY 2003-10-28 US disclosed
EP-1303514-A1 PROCESS FOR PREPARING AZACYCLOALKANOYLAMINOTHIAZOLES Bristol-Myers Squibb Company (US) 2003-04-23 EP disclosed
US-6534531-B2 Thiazole derivatives BRISTOL-MYERS SQUIBB COMPANY 2003-03-18 US disclosed
US-20020099217-A1 Process for preparing azacycloalkanoylaminothiazoles CHEN BANG-CHI (US) 2002-07-25 US disclosed
US-6414156-B2 EFFICENT, NOTOXIC PROCESS OF MAKING NEW KEY INTERMEDIATE QUATERNARY AMMONIUM SALTS AND 2-OXAZOLYLALKYL SULFIDE DERIVATIVES AND AVOIDS THE REACTION OF A-HALOKETONES WITH AN AZIDE FOLLOWED BY REDUCING THE RESULTING A-AMINOKETONE BRISTOL-MYERS SQUIBB COMPANY 2002-07-02 US disclosed
US-20020061915-A1 Methods for preventing and treating alopecia induced by chemotherapy or radiotherapy BRISTOL-MYERS SQUIBB COMPANY 2002-05-23 US disclosed
WO-2002010163-A1 PROCESS FOR PREPARING AZACYCLOALKANOYLAMINOTHIAZOLES BRISTOL-MYERS SQUIBB COMPANY (US) 2002-02-07 WO disclosed
US-20010006976-A1 Process for preparing azacycloalkanoylaminothiazoles BRISTOL-MYERS SQUIBB COMPANY 2001-07-05 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 (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-20020099217-A1 Process for preparing azacycloalkanoylaminothiazoles CDK9, CDK4, CDK6 CDK4 2/4885KDR 2135/4885CDK2 15/4885
US-20010006976-A1 Process for preparing azacycloalkanoylaminothiazoles CDK9, CDK4, CDK6 CDK4 2/4885KDR 2135/4885CDK2 15/4885
US-20020061915-A1 Methods for preventing and treating alopecia induced by chemotherapy or radiotherapy NR5A1, CYP17A1, CYP21A2 CDK4 3822/4885KDR 4417/4885CDK2 2778/4885
US-20040063767-A1 Process for preparing azacycloalkanoylaminothiazoles (LD 137e) CDK9, CDK4, CCNI CDK4 2/4885KDR 2756/4885CDK2 19/4885

“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.