SCHEMBL133955

SCHEMBL133955

N[C@@H]1C[C@H](N)[C@@H](O)[C@H](O)[C@H]1O

nearest known ligand 0.71

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
FUCA1 P04066 4/20 0.63
SI P14410 2/20 0.57
GBA1 P04062 2/20 0.44
MGAM O43451 1/20 0.39
GAA P10253 1/20 0.39
LMNA P02545 1/20 0.39
APP P05067 1/20 0.39
LRAT O95237 1/20 0.34
GABRR1 P24046 1/20 0.33
CYP2C9 P11712 1/20 0.30

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
SCHEMBL11044942 1.00 FUCA1 (0.63) FUCA1SIGBA1MGAMGAA
SCHEMBL18460913 1.00 FUCA1 (0.63) FUCA1SIGBA1MGAMGAA
SCHEMBL21105130 1.00 FUCA1 (0.63) FUCA1SIGBA1MGAMGAA
Bromide SCHEMBL6284958 0.96 FUCA1 (0.60) FUCA1SIGBA1MGAMGAA
SCHEMBL5805992 0.96
SCHEMBL11049253 0.88
Carbamic Acid SCHEMBL6209325 0.85 FUCA1 (0.50) FUCA1SIGBA1MGAMGAA
SCHEMBL29379044 0.83 FUCA1 (0.55) FUCA1SIGBA1MGAMGAA
SCHEMBL374134 0.83 FUCA1 (0.55) FUCA1SIGBA1MGAMGAA
SCHEMBL21105031 0.81 GBA1 (0.50) FUCA1SIGBA1MGAMGAA

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 1068 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106591401-A Fermentation promoter for improving output of gentamycin C1a, and adding method thereof 河南仁华生物科技有限公司 2017-04-26 CN claimed
EP-2069500-B1 COMPOSITIONS COMPRISING A SIRNA AND LIPIDIC 4,5-DISUBSTITUTED 2-DEOXYSTREPTAMINE RING AMINOGLYCOSIDE DERIVATIVES AND USES THEREOF CENTRE NAT RECH SCIENT (FR) 2014-09-24 EP claimed
CN-101918577-B Novel aminoglycoside antibiotic, method for producing the same, and pharmaceutical use of the same MEIJI SEIKA KAISHA 2014-03-26 CN claimed
CN-101918577-A Novel aminoglycoside antibiotic, method for producing the same, and pharmaceutical use of the same MEIJI SEIKA KAISHA 2010-12-15 CN claimed
US-20100311680-A1 SYNTHESIS OF NOVEL NEAMINE DERIVATIVES AND USE THEREOF AS ANTIBACTERIAL AGENTS UNIVERSITE JOSEPH FOURIER (FR) 2010-12-09 US claimed
EP-2235031-A2 SYNTHESIS OF NOVEL NEAMINE DERIVATIVES AND USE THEREOF AS ANTIBACTERIAL AGENTS Université Joseph Fourier (FR) 2010-10-06 EP claimed
CN-101772347-A The 2-amino-2 of sense single stranded rna enveloped virus, the two deoxidation-α of 7--D-glycerol-D-glucose-pyrans heptose base inhibitor INST HEPATITIS & VIRUS RES 2010-07-07 CN claimed
EP-2197451-A1 2-AMINO-2,7-DIDEOXY-ALPHA-D-GLYCERO-D-GLUCO-HEPTOPYRANOSYL INHIBITORS OF POSITIVE SENSE SINGLE-STRANDED RNA ENVELOPE VIRUSES Institute For Hepatitis And Virus Research (US) 2010-06-23 EP claimed
US-20100035974-A1 COMPOSITIONS COMPRISING A SIRNA AND LIPIDIC 4,5-DISUBSTITUTED 2-DEOXYSTREPTAMINE RING AMINOGLYCOSIDE DERIVATIVES AND USES THEREOF CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS (FR) 2010-02-11 US claimed
WO-2009095588-A2 SYNTHESIS OF NOVEL NEAMINE DERIVATIVES AND USE THEREOF AS ANTIBACTERIAL AGENTS UNIVERSITE JOSEPH FOURIER (FR) 2009-08-06 WO claimed
US-4424344-A 2-N-Acylated and 2-N-alkylated derivatives of 4-O-substituted-2-deoxystreptamine aminoglycosides and process ELI LILLY AND COMPANY (US) 1984-01-03 US claimed
EP-0048614-A1 1-N-acylated and 1-N-alkylated derivatives of 4-0-substituted -2-deoxystreptamine aminoglycosides ELI LILLY AND COMPANY (US) 1982-03-31 EP claimed
EP-0048613-A1 4-0-Substituted -2-deoxystreptamine aminoglycoside derivatives, their preparation and formulations containing them ELI LILLY AND COMPANY (US) 1982-03-31 EP claimed
US-4212860-A COUPLING THE PENTOFURANOSYL ONTO THE PROTECTED CYCLITOL SCHERING CORPORATION (US) 1980-07-15 US claimed
US-4171356-A 2-Unsubstituted derivatives of 4,6-di-o-(aminoglycosyl)-1,3-diaminocyclitois, methods for their use as antibacterial agents and compositions useful therefor SCHERING CORPORATION (US) 1979-10-16 US claimed
US-4170641-A 1-N-(ω-aminoalkanesulfonyl) derivative of aminoglycosidic antibiotic and process for preparation thereof MEIJI SEIKA KAISHA, LTD. (JP) 1979-10-09 US claimed
US-4125707-A ANTIBIOTIC SOCIETA' FARMACEUTICI ITALIA S.P.A. (IT) 1978-11-14 US claimed
US-4085208-A Process for preparing 4,6-di-O-(aminoglycosyl)-1,3-diaminocyclitols and novel 1-epimers and 1-N-alkyl derivatives produced thereby; methods for the use of the 1-epimer derivatives as antibacterial agents and compositions useful therefor SCHERING CORPORATION (US) 1978-04-18 US claimed
US-4062947-A Di-N-alkylaminoglycosides, methods for their manufacture and novel intermediates useful therein, method for their use as antibacterial agents and pharmaceutical compositions useful therefor SCHERING CORPORATION (US) 1977-12-13 US claimed
US-3982996-A CULTURING STERLING DRUG INC. (US) 1976-09-28 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20100311680-A1 SYNTHESIS OF NOVEL NEAMINE DERIVATIVES AND USE THEREOF AS ANTIBACTERIAL AGENTS HRH3, HRH4, H1-4 FUCA1 4799/4885SI 3165/4885GBA1 4069/4885
US-20100035974-A1 COMPOSITIONS COMPRISING A SIRNA AND LIPIDIC 4,5-DISUBSTITUTED 2-DEOXYSTREPTAMINE RING AMINOGLYCOSIDE DERIVATIVES AND USES THEREOF STARD3, NSUN3, NR1H4 FUCA1 2564/4885SI 3188/4885GBA1 3213/4885

“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.