SCHEMBL1914213

SCHEMBL1914213

O=C(O)/C=C/c1ccc(-c2ccc(O)c(C34CC5CC(CC(C5)C3)C4)c2)c(Cl)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PTPN11 Q06124 13/20 1.00
NR0B2 Q15466 4/20 1.00
RARB P10826 3/20 0.74
PTPRCAP Q14761 2/20 0.63
HDAC4 P56524 2/20 0.59
HDAC7 Q8WUI4 2/20 0.59
HDAC11 Q96DB2 2/20 0.59
HDAC8 Q9BY41 2/20 0.59
HDAC6 Q9UBN7 2/20 0.59
HDAC9 Q9UKV0 2/20 0.59
HDAC3 O15379 1/20 0.59
HDAC2 Q92769 1/20 0.59
HDAC5 Q9UQL6 1/20 0.59
HDAC1 Q13547 1/20 0.58
HDAC10 Q969S8 1/20 0.58
RARA P10276 1/20 0.55
RARG P13631 1/20 0.55

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
SCHEMBL29604865 1.00 PTPN11 (1.00) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL1914215 1.00 PTPN11 (1.00) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL12257833 0.91 PTPN11 (0.83) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL2389152 0.89 RARB (0.80) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL2389155 0.89 RARB (0.80) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL3289761 0.89 PTPN11 (0.80) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL3289754 0.89 PTPN11 (0.80) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL2391213 0.87 PTPN11 (0.77) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL2391204 0.87 PTPN11 (0.77) PTPN11NR0B2RARBPTPRCAPHDAC4
SCHEMBL2407028 0.87 PTPN11 (0.77) PTPN11NR0B2RARBPTPRCAPHDAC4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2020198576-A1 METHODS OF MODULATING REGULATORY T CELLS THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2020-10-01 WO disclosed
WO-2020130863-A1 METHODS OF TREATMENT OF CANCER ASSOCIATED WITH CENTROSOME AMPLIFICATION INSTITUTO DE MEDICINA MOLECULAR (PT) 2020-06-25 WO disclosed
US-9096544-B2 Therapeutic compounds WAYNE STATE UNIVERSITY (US) 2015-08-04 US disclosed
US-9096544-B2 Therapeutic compounds WAYNE STATE UNIVERSITY (US) 2015-08-04 US disclosed
US-9096544-B2 Therapeutic compounds WAYNE STATE UNIVERSITY (US) 2015-08-04 US disclosed
EP-2367781-B1 RETINOID DERIVATIVES ENDOWED WITH CYTOTOXIC AND/OR ANTIANGIOGENIC PROPERTIES SIGMA TAU IND FARMACEUTI (IT) 2013-10-02 EP disclosed
US-8530517-B2 Retinoid derivatives endowed with cytotoxic and/or antiangiogenic properties SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A. (IT) 2013-09-10 US disclosed
US-20130137699-A1 THERAPEUTIC COMPOUNDS NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2013-05-30 US disclosed
US-20130137699-A1 THERAPEUTIC COMPOUNDS NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2013-05-30 US disclosed
US-20130137699-A1 THERAPEUTIC COMPOUNDS NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2013-05-30 US disclosed
WO-2008033466-A2 COMPOSITIONS AND METHODS FOR TREATMENT OF VIRAL DISEASES COMBINATORX (SINGAPORE) PRE. LTD. (SG) 2008-03-20 WO disclosed
EP-1896399-A1 BIPHENYL AND NAPHTHYL-PHENYL HYDROXAMIC ACID DERIVATIVES SIGMA-TAU Industrie Farmaceutiche Riunite S.p.A. (IT) 2008-03-12 EP disclosed
CN-100348569-C Induction of apoptosis in cancer cells BURNHAM INST (US) 2007-11-14 CN disclosed
WO-2007000383-A1 BIPHENYL AND NAPHTHYL-PHENYL HYDROXAMIC ACID DERIVATIVES SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A. (IT) 2007-01-04 WO disclosed
WO-2007000383-A1 BIPHENYL AND NAPHTHYL-PHENYL HYDROXAMIC ACID DERIVATIVES SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A. (IT) 2007-01-04 WO disclosed
US-7053071-B2 For therapy of leukemia or other forms of cancer or for treating disease conditions caused by apoptosis of cells THE BURNHAM INSTITUTE (US) 2006-05-30 US disclosed
CN-1659130-A Induction of apoptosis in cancer cells BURNHAM INST (US) 2005-08-24 CN disclosed
EP-1456165-A1 INDUCTION OF APOPTOSIS IN CANCER CELLS The Burnham Institute (US) 2004-09-15 EP disclosed
US-20030176506-A1 Induction of apoptosis in cancer cells BURNHAM INSTITUTE FOR MEDICAL RESEARCH 2003-09-18 US disclosed
WO-2003048101-A1 INDUCTION OF APOPTOSIS IN CANCER CELLS THE BURNHAM INSTITUTE (US) 2003-06-12 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 (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-20130137699-A1 THERAPEUTIC COMPOUNDS BAX, MCL1, TMBIM6 PTPN11 2827/4885NR0B2 3403/4885RARB 3599/4885
US-20030176506-A1 Induction of apoptosis in cancer cells MCL1, BAD, BCL2 PTPN11 2842/4885NR0B2 2377/4885RARB 577/4885

“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.