SCHEMBL3513607

SCHEMBL3513607

CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2cc3cc(O)c(O)cc3nc2-1

nearest known ligand 0.86

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TOP1 P11387 18/20 0.86
MEN1 O00255 4/20 0.80
KMT2A Q03164 4/20 0.80
SMN1; SMN2 Q16637 4/20 0.80
ALDH1A1 P00352 4/20 0.80
KDM4E B2RXH2 3/20 0.80
CYP3A4 P08684 2/20 0.80
HBB P68871 2/20 0.80
DDX5 P17844 1/20 0.80
CASP1 P29466 1/20 0.80
CASP7 P55210 1/20 0.80
GLA P06280 3/20 0.77
TP53 P04637 2/20 0.77
HPGD P15428 2/20 0.77
STAT6 P42226 1/20 0.77
CHEK1 O14757 1/20 0.77
HDAC3 O15379 1/20 0.77
ABCC4 O15439 1/20 0.77
GMNN O75496 1/20 0.77
LMNA P02545 1/20 0.77

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
SCHEMBL27764694 1.00 TOP1 (0.86) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL16649109 0.93 TOP1 (0.78) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL23929259 0.93 TOP1 (1.00) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL23963902 0.93 TOP1 (1.00) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL16649363 0.91 TOP1 (0.79) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL3138027 0.90 TOP1 (0.82) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL18251453 0.90 TOP1 (0.73) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
Hydroxycamptothecin SCHEMBL29350707 0.89 TOP1 (1.00) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
Hydroxycamptothecin SCHEMBL9384413 0.89 TOP1 (1.00) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1
Hydroxycamptothecin SCHEMBL25875 0.89 TOP1 (1.00) TOP1MEN1KMT2ASMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240084272-A1 CYTOCHROME P450 MONOOXYGENASES AND USES THEREOF UNIV BRITISH COLUMBIA (CA) 2024-03-14 US claimed
WO-2022120490-A1 CYTOCHROME P450 MONOOXYGENASES AND USES THEREOF THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2022-06-16 WO claimed
US-6011042-A POLYMERIC PRODRUGS ARE PREFERABLY ESTERS OF HYDROXYL-CONTAINING AROMATIC COMPOUNDS AND ARE FORMED BY REACTING A DESIRED AROMATIC, HYDROXYL-CONTAINING COMPOUND WITH A SUBSTANTIALLY NON-ANTIGENIC POLYMER ENZON, INC. (US) 2000-01-04 US claimed
US-20240084272-A1 CYTOCHROME P450 MONOOXYGENASES AND USES THEREOF UNIV BRITISH COLUMBIA (CA) 2024-03-14 US disclosed
WO-2022120490-A1 CYTOCHROME P450 MONOOXYGENASES AND USES THEREOF THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2022-06-16 WO disclosed
US-8367065-B2 Targeted polymeric prodrugs containing multifunctional linkers ENZON PHARMACEUTICALS, INC. (US) 2013-02-05 US disclosed
US-20100233190-A1 TARGETED POLYMERIC PRODRUGS CONTAINING MULTIFUNCTIONAL LINKERS ENZON PHARMACEUTICALS, INC. (US) 2010-09-16 US disclosed
EP-2073820-A2 TARGETED POLYMERIC PRODRUGS CONTAINING MULTIFUNCTIONAL LINKERS Enzon Pharmaceuticals, Inc. (US) 2009-07-01 EP disclosed
WO-2008034124-A2 TARGETED POLYMERIC PRODRUGS CONTAINING MULTIFUNCTIONAL LINKERS ENZON PHARMACEUTICALS, INC. (US) 2008-03-20 WO disclosed
EP-0963988-B1 Intermediates for making camptothecin and camptothecin analogs UNIV NORTH CAROLINA STATE (US) 2005-04-27 EP disclosed
EP-0923566-B1 HIGH MOLECULAR WEIGHT POLYMER-BASED PRODRUGS ENZON INC (US) 2003-10-29 EP disclosed
US-5264579-A D ring intermediates for the synthesis of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-11-23 US disclosed
US-5258516-A Optically pure D,E ring intermediates useful for the synthesis of camptothecin and camptothecin analogs NC STATE UNIVERSITY (US) 1993-11-02 US disclosed
US-5254690-A Alkoxymethylpyridine d-ring intermediates useful for the synthesis of camptpthecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-10-19 US disclosed
US-5247089-A Method of making intermediates useful for the manufacture of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-09-21 US disclosed
US-5243050-A Alkylpyridone DE ring intermediates useful for the manufacture of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-09-07 US disclosed
US-5212317-A Methods and intermediates for the assymmetric synthesis of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-05-18 US disclosed
US-5200524-A Camptothecin intermediates and method of making same NORTH CAROLINA STATE UNIVERSITY (US) 1993-04-06 US disclosed
US-5191082-A Camptothecin intermediate and method of making camptothecin intermediates NORTH CAROLINA STATE UNIVERSITY (US) 1993-03-02 US disclosed
US-5162532-A INTERMEDIATES AND METHOD OF MAKING CAMPTOTHECIN AND CAMPTOTHECIN ANALOGS NORTH CAROLINA STATE UNIVERSITY (US) 1992-11-10 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 (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-20100233190-A1 TARGETED POLYMERIC PRODRUGS CONTAINING MULTIFUNCTIONAL LINKERS PAICS, FCGRT, DNPEP TOP1 1503/4885MEN1 2219/4885KMT2A 2107/4885
US-20240084272-A1 CYTOCHROME P450 MONOOXYGENASES AND USES THEREOF CYP3A43, CYP11B2, CYP11B1 TOP1 367/4885MEN1 2868/4885KMT2A 3443/4885

“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.