SCHEMBL2340689

SCHEMBL2340689

C=C(CC(NC(=O)c1ccc(NCc2cnc3nc(N)[nH]c(=O)c3n2)cc1)C(=O)O)C(=O)O

nearest known ligand 0.76

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ TYMS P04818 3/20 0.76
▸ AKR1B1 P15121 2/20 0.76
▸ KDM4E B2RXH2 1/20 0.76
▸ MEN1 O00255 1/20 0.76
▸ ALDH1A1 P00352 1/20 0.76
▸ POLB P06746 1/20 0.76
▸ GAA P10253 1/20 0.76
▸ HPGD P15428 1/20 0.76
▸ TSHR P16473 1/20 0.76
▸ PTGS2 P35354 1/20 0.76
▸ KMT2A Q03164 1/20 0.76
▸ HSD17B10 Q99714 1/20 0.76
▸ TDP1 Q9NUW8 1/20 0.76
▸ DHFR P00374 8/20 0.75
▸ ADORA3 P0DMS8 1/20 0.55
▸ GART P22102 2/20 0.51
▸ ATIC P31939 1/20 0.51
▸ NOS1 P29475 1/20 0.44

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
SCHEMBL31683754 0.92 TYMS (0.79) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL30078194 0.91 TYMS (0.84) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL30078267 0.91 AKR1B1 (0.80) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL30078340 0.89 TYMS (0.82) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL29907321 0.89 AKR1B1 (0.82) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL470145 0.88 AKR1B1 (0.81) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL10173120 0.88 AKR1B1 (0.81) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL30174303 0.88 AKR1B1 (0.81) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL12523472 0.88 AKR1B1 (0.81) TYMSAKR1B1KDM4EMEN1ALDH1A1
SCHEMBL15094347 0.88 AKR1B1 (0.81) TYMSAKR1B1KDM4EMEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10466253-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-11-05 — — US disclosed
US-20170350903-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2017-12-07 — — US disclosed
US-9778268-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2017-10-03 — — US disclosed
US-9720002-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2017-08-01 — — US disclosed
US-9043159-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2015-05-26 — — US disclosed
US-9037417-B2 Molecular flux rates through critical pathways measured by stable isotope labeling In Vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2015-05-19 — — US disclosed
US-20140295484-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2014-10-02 — — US disclosed
US-20140295485-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2014-10-02 — — US disclosed
US-8849581-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2014-09-30 — — US disclosed
US-20140193828-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2014-07-10 — — US disclosed
US-20130273533-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2013-10-17 — — US disclosed
US-8401800-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2013-03-19 — — US disclosed
US-20120115127-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-05-10 — — US disclosed
US-8005623-B2 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2011-08-23 — — US disclosed
CN-100469361-C Method and composition for treating or preventing catabolism or stimulating anabolism in a mammal undergoing metabolic stress NUTRICIA NV (NL) 2009-03-18 — — CN disclosed
EP-1759326-A4 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY UNIV CALIFORNIA (US) 2008-10-22 — — EP disclosed
EP-1759326-A2 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2007-03-07 — — EP disclosed
US-20060020440-A1 Molecular flux rates through critical pathways measured by stable isotope labeling in vivo, as biomarkers of drug action and disease activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2006-01-26 — — US disclosed
CN-1674795-A Method and composition for treating or preventing catabolism or stimulating anabolism in a mammal undergoing metabolic stress NUTRICIA NV (NL) 2005-09-28 — — CN disclosed
WO-2005081943-A2 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2005-09-09 — — 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 (1 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-20120115127-A1 MOLECULAR FLUX RATES THROUGH CRITICAL PATHWAYS MEASURED BY STABLE ISOTOPE LABELING IN VIVO, AS BIOMARKERS OF DRUG ACTION AND DISEASE ACTIVITY GOT2, PC, PCK2 TYMS 1024/4885AKR1B1 132/4885KDM4E 4701/4885

“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.

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