SCHEMBL842438

SCHEMBL842438

Nc1nc(I)nc2nc[nH]c12

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PDPK1 O15530 1/20 0.66
▸ GDA Q9Y2T3 1/20 0.66
▸ CDK2 P24941 3/20 0.56
▸ PI4KA P42356 2/20 0.52
▸ PI4K2B Q8TCG2 2/20 0.52
▸ PI4K2A Q9BTU6 2/20 0.52
▸ PI4KB Q9UBF8 2/20 0.52
▸ LMNA P02545 1/20 0.52
▸ DRD3 P35462 1/20 0.52
▸ XDH P47989 1/20 0.52
▸ LRRK2 Q5S007 1/20 0.52
▸ DPP4 P27487 1/20 0.47
▸ PNP P00491 1/20 0.46
▸ POLA1 P09884 2/20 0.43
▸ MAP3K5 Q99683 1/20 0.43
▸ ADORA1 P30542 1/20 0.43
▸ HTR2B P41595 1/20 0.43
▸ ALDH1A1 P00352 2/20 0.41
▸ CDK1 P06493 2/20 0.40
▸ CCNB1 P14635 2/20 0.40

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
SCHEMBL31350217 1.00 PDPK1 (0.66) PDPK1GDACDK2PI4KAPI4K2B
2,6-Diaminopurine SCHEMBL24053 0.79 PDPK1 (1.00) PDPK1GDACDK2PI4KAPI4K2B
SCHEMBL532461 0.79 CDK2 (0.66) PDPK1GDACDK2PI4KAPI4K2B
2,6-Diaminopurine SCHEMBL8757979 0.78 PDPK1 (0.96) PDPK1GDACDK2PI4KAPI4K2B
2,6-Diaminopurine SCHEMBL27891733 0.78 PDPK1 (0.96) PDPK1GDACDK2PI4KAPI4K2B
2,6-Diaminopurine SCHEMBL28206545 0.78 PDPK1 (0.96) PDPK1GDACDK2PI4KAPI4K2B
SCHEMBL8851 0.76 PDPK1 (0.66) PDPK1GDACDK2PI4KAPI4K2B
SCHEMBL19780 0.76 PDPK1 (0.66) PDPK1GDACDK2PI4KAPI4K2B
SCHEMBL16147074 0.76 CDK2 (0.47) PDPK1GDACDK2PI4KAPI4K2B
SCHEMBL2352414 0.76 DPP4 (0.61) PDPK1GDACDK2XDHDPP4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170175129-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS INC (US) 2017-06-22 — — US claimed
US-20170136131-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF Modema Therapeutics, Inc. (US) 2017-05-18 — — US claimed
EP-3157572-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2017-04-26 — — EP claimed
EP-3157573-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2017-04-26 — — EP claimed
US-20160304552-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. 2016-10-20 — — US claimed
EP-3080289-A2 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2016-10-19 — — EP claimed
WO-2015196130-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-12-23 — — WO claimed
WO-2015196128-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-12-23 — — WO claimed
US-20150307542-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNATX, INC. 2015-10-29 — — US claimed
EP-2931319-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2015-10-21 — — EP claimed
WO-2015089511-A2 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-06-18 — — WO claimed
US-20140303112-A1 Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) ENERGENESIS BIOMEDICAL CO., LTD (TW) 2014-10-09 — — US claimed
WO-2014093924-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2014-06-19 — — WO claimed
US-20110015383-A1 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2011-01-20 — — US claimed
US-20100137576-A1 5' O [(N ACYL)AMIDOPHOSPHATE] AND 5' O [(N ACYL)AMIDOTHIOPHOSPHATE] AND 5' O [(N ACYL)AMIDODITHIOPHOSPHATE] AND 5' O [(N ACYL)AMIDOSELENOPHOSPHATE] DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF CENTRUM BADAN MILEKULARNYCHI MAKROMOLEKULARNYCH, P (PL) 2010-06-03 — — US claimed
EP-2170918-A2 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF Centrum Badan Molekularnych I Makromolekularnych Pan (PL) 2010-04-07 — — EP claimed
EP-2097430-A1 5'-O-[(N-ACYL)AMIDOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDOTHIOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDODITHIOPHOSPHATE]- AND 5'-O-[N- ACYL)AMIDOSELENOPHOSPHATE-DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF Centrum Badan Molekularnych I Makromolekularnych Pan (PL) 2009-09-09 — — EP claimed
WO-2009005382-A2 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2009-01-08 — — WO claimed
WO-2008048128-A1 5'-O-[(N-ACYL)AMIDOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDOTHIOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDODITHIOPHOSPHATE]- AND 5'-O-[(N- ACYL)AMIDOSELENOPHOSPHATE]-DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2008-04-24 — — WO claimed
EP-4731186-A2 METHODS AND COMPOSITIONS FOR TREATING EPITHELIAL DISEASES The Regents of the University of California (US) 2026-04-29 — — EP disclosed
WO-2024263919-A2 METHODS AND COMPOSITIONS FOR TREATING EPITHELIAL DISEASES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-12-26 — — WO disclosed
US-20240165267-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF ARES CAPITAL CORPORATION, AS AGENT 2024-05-23 — — US disclosed
CN-116492347-A Compound for activating AMPK and application thereof 华安医学股份有限公司 2023-07-28 — — CN disclosed
US-20230013636-A1 EXOSOMES-BASED THERAPY FOR LIVER FIBROSIS AND OTHER DISEASES WITH FIBROSIS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2023-01-19 — — US disclosed
CN-115297850-A Exosome-based treatment for liver fibrosis and other fibrosis-related diseases 得克萨斯州大学系统董事会 2022-11-04 — — CN disclosed
EP-4069205-A1 EXOSOMES-BASED THERAPY FOR LIVER FIBROSIS AND OTHER DISEASES ASSOCIATED WITH FIBROSIS Board of Regents, The University of Texas System (US) 2022-10-12 — — EP disclosed
US-20220064732-A1 METHODS FOR TREATING PARKINSON'S DISEASE BPGBIO, INC. 2022-03-03 — — US disclosed
US-20210252036-A1 METHODS OF TREATING CANCER BY INHIBITING UBIQUITIN CONJUGATING ENZYME E2 K (UBE2K) THLIVERIS, ANDREW T. 2021-08-19 — — US disclosed
CN-108645832-B SERS chip and preparation method and application thereof 苏州英菲尼纳米科技有限公司 2021-07-27 — — CN disclosed
EP-3849543-A1 METHODS OF TREATING CANCER BY INHIBITING UBIQUITIN CONJUGATING ENZYME E2 K (UBE2K) Berg LLC (US) 2021-07-21 — — EP disclosed
CN-112996504-A Methods of treating cancer by inhibiting ubiquitin conjugating enzyme E2K (UBE2K) 博格有限责任公司 2021-06-18 — — CN disclosed
WO-2021113761-A1 EXOSOMES-BASED THERAPY FOR LIVER FIBROSIS AND OTHER DISEASES ASSOCIATED WITH FIBROSIS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2021-06-10 — — WO disclosed
US-11001891-B2 Methods for treating Parkinson's disease BERG LLC (US) 2021-05-11 — — US disclosed
WO-2020055906-A1 METHODS OF TREATING CANCER BY INHIBITING UBIQUITIN CONJUGATING ENZYME E2 K (UBE2K) BERG LLC (US) 2020-03-19 — — WO disclosed
EP-3538095-A1 METHODS FOR TREATING PARKINSON'S DISEASE Berg LLC (US) 2019-09-18 — — EP disclosed
US-20190255194-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNATX INC (US) 2019-08-22 — — US disclosed
EP-2931319-B1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNATX INC (US) 2019-08-21 — — EP disclosed
US-10286086-B2 Alternative nucleic acid molecules and uses thereof MODERNATX, INC. (US) 2019-05-14 — — US disclosed
EP-2854865-B1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA BERG LLC (US) 2019-02-20 — — EP disclosed
US-10023864-B2 Methods of treating a metabolic syndrome by modulating heat shock protein (HSP) 90-beta BERG LLC (US) 2018-07-17 — — US disclosed
WO-2018090054-A1 METHODS FOR TREATING PARKINSON'S DISEASE BERG LLC (US) 2018-05-17 — — WO disclosed
US-20180135129-A1 METHODS FOR TREATING PARKINSON'S DISEASE BERG, KARA ANN 2018-05-17 — — US disclosed
US-9938279-B2 Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) ENERGENESIS BIOMEDICAL CO., LTD (TW) 2018-04-10 — — US disclosed
US-20170175129-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS INC (US) 2017-06-22 — — US disclosed
US-20170166891-A1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA BERG PHARMA LLC 2017-06-15 — — US disclosed
US-20170136131-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF Modema Therapeutics, Inc. (US) 2017-05-18 — — US disclosed
US-20170136132-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2017-05-18 — — US disclosed
EP-3168304-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS Ophthotech Corporation (US) 2017-05-17 — — EP disclosed
EP-3165606-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES Ophthotech Corporation (US) 2017-05-10 — — EP disclosed
EP-3157572-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2017-04-26 — — EP disclosed
EP-3157573-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2017-04-26 — — EP disclosed
EP-3152307-A2 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA Berg LLC (US) 2017-04-12 — — EP disclosed
US-9533002-B2 Methods of treating a metabolic syndrome by modulating heat shock protein (HSP) 90-β BERG LLC (US) 2017-01-03 — — US disclosed
US-20160354493-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNATX, INC. 2016-12-08 — — US disclosed
US-20160354491-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS INC (US) 2016-12-08 — — US disclosed
US-20160354492-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS INC (US) 2016-12-08 — — US disclosed
US-20160354490-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS INC (US) 2016-12-08 — — US disclosed
US-20160348099-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS INC (US) 2016-12-01 — — US disclosed
US-20160304552-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. 2016-10-20 — — US disclosed
EP-3080289-A2 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2016-10-19 — — EP disclosed
US-20160264969-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES OPHTHOTECH CORPORATION 2016-09-15 — — US disclosed
EP-1919930-B1 NEW NUCLEIC ACID BASE PAIRS DAKO DENMARK AS (DK) 2016-09-14 — — EP disclosed
EP-3028707-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES Ophthotech Corporation (US) 2016-06-08 — — EP disclosed
WO-2015196118-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-12-23 — — WO disclosed
WO-2015196128-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-12-23 — — WO disclosed
WO-2015196130-A2 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-12-23 — — WO disclosed
US-20150353930-A1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA BERG LLC 2015-12-10 — — US disclosed
US-20150307542-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNATX, INC. 2015-10-29 — — US disclosed
EP-2931319-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF Moderna Therapeutics, Inc. (US) 2015-10-21 — — EP disclosed
US-20150202288-A1 Combination Therapy for the Treatment of Ocular Neovascular Disorders EYETECH PHARMACEUTICALS, INC. 2015-07-23 — — US disclosed
US-20150202289-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS EYETECH PHARMACEUTICALS, INC. 2015-07-23 — — US disclosed
US-20150182623-A1 Compositions Comprising an Anti-PDGF Aptamer and a VEGF Antagonist Integrity Bio, Inc. 2015-07-02 — — US disclosed
WO-2015089511-A2 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2015-06-18 — — WO disclosed
US-20150157709-A1 Compositions Comprising an Anti-PDGF Aptamer and a VEGF Antagonist Integrity Bio, Inc. 2015-06-11 — — US disclosed
EP-2854844-A2 COMPOSITIONS COMPRISING AN ANTI-PDGF APTAMER AND A VEGF ANTAGONIST Ophthotech Corporation (US) 2015-04-08 — — EP disclosed
EP-2854865-A2 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA Berg LLC (US) 2015-04-08 — — EP disclosed
US-8916570-B2 A3 adenosine receptor agonists and antagonists THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2014-12-23 — — US disclosed
US-20140303112-A1 Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) ENERGENESIS BIOMEDICAL CO., LTD (TW) 2014-10-09 — — US disclosed
US-20140294816-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS EYETECH PHARMACEUTICALS, INC. 2014-10-02 — — US disclosed
US-20140242082-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS OPHTHOTECH CORPORATION (US) 2014-08-28 — — US disclosed
US-20140179621-A1 Methods for Treating or Preventing Ophthalmological Diseases OPHTHOTECH CORPORATION (US) 2014-06-26 — — US disclosed
WO-2014093924-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF MODERNA THERAPEUTICS, INC. (US) 2014-06-19 — — WO disclosed
US-20140154266-A1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA BERG PHARMA LLC (US) 2014-06-05 — — US disclosed
WO-2013181495-A2 COMPOSITIONS COMPRISING AN ANTI-PDGF APTAMER AND A VEGF ANTAGONIST OPHTHOTECH CORPORATION (US) 2013-12-05 — — WO disclosed
US-20130323242-A1 COMPOSITIONS COMPRISING AN ANTI-PDGF APTAMER AND A VEGF ANTAGONIST OPHTHOTECH CORP. (US) 2013-12-05 — — US disclosed
WO-2013177535-A2 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA BERG PHARMA LLC (US) 2013-11-28 — — WO disclosed
US-20120184569-A1 A3 ADENOSINE RECEPTOR AGONISTS AND ANTAGONISTS THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES (US) 2012-07-19 — — US disclosed
US-8206707-B2 Combination therapy for the treatment of ocular neovascular disorders OPHTHOTECH CORPORATION (US) 2012-06-26 — — US disclosed
US-8187597-B2 Combination therapy for the treatment of ocular neovascular disorders OPHTHOTECH CORPORATION (US) 2012-05-29 — — US disclosed
EP-1660057-B1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS OPHTHOTECH CORP (US) 2012-05-23 — — EP disclosed
US-20120100136-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES OPHTHOTECH CORPORATION (US) 2012-04-26 — — US disclosed
EP-2432476-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES Ophthotech Corporation (US) 2012-03-28 — — EP disclosed
US-20110200593-A1 Combination Therapy for the Treatment of Ocular Neovascular Disorders OPHTHOTECH CORPORATION 2011-08-18 — — US disclosed
EP-2281885-A1 Combination therapy for the treatment of ocular neovascular disorders Ophthotech Corporation (US) 2011-02-09 — — EP disclosed
US-20110015383-A1 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2011-01-20 — — US disclosed
WO-2010127029-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES OPHTHOTECH CORPORATION (US) 2010-11-04 — — WO disclosed
US-7785784-B2 Detection of oligonucleotides by dual hybridization Eyetech, Inc. (US) 2010-08-31 — — US disclosed
US-7759472-B2 Administering platelet derived growth factor antagonist and endothelial growth factor antagonist OPHTHOTECH CORPORATION (US) 2010-07-20 — — US disclosed
US-20100137576-A1 5' O [(N ACYL)AMIDOPHOSPHATE] AND 5' O [(N ACYL)AMIDOTHIOPHOSPHATE] AND 5' O [(N ACYL)AMIDODITHIOPHOSPHATE] AND 5' O [(N ACYL)AMIDOSELENOPHOSPHATE] DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF CENTRUM BADAN MILEKULARNYCHI MAKROMOLEKULARNYCH, P (PL) 2010-06-03 — — US disclosed
US-20100129364-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS OPHTHOTECH CORPORATION (US) 2010-05-27 — — US disclosed
US-20100119522-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS OPHTHOTECH CORPORATION (US) 2010-05-13 — — US disclosed
US-20100111942-A1 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS OPHTHOTECH CORPORATION (US) 2010-05-06 — — US disclosed
EP-2170918-A2 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF Centrum Badan Molekularnych I Makromolekularnych Pan (PL) 2010-04-07 — — EP disclosed
EP-2170918-A2 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF Centrum Badan Molekularnych I Makromolekularnych Pan (PL) 2010-04-07 — — EP disclosed
US-7645871-B2 Tumor inhibition by modulating sprouty expression of activity MICHIGAN STATE UNIVERSITY (US) 2010-01-12 — — US disclosed
EP-2099497-A2 ENHANCED RETINAL DELIVERY OF A NUCLEIC ACID THROUGH IONTOPHORESIS Eyegate Pharma SA (FR) 2009-09-16 — — EP disclosed
EP-2097430-A1 5'-O-[(N-ACYL)AMIDOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDOTHIOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDODITHIOPHOSPHATE]- AND 5'-O-[N- ACYL)AMIDOSELENOPHOSPHATE-DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF Centrum Badan Molekularnych I Makromolekularnych Pan (PL) 2009-09-09 — — EP disclosed
EP-2097430-A1 5'-O-[(N-ACYL)AMIDOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDOTHIOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDODITHIOPHOSPHATE]- AND 5'-O-[N- ACYL)AMIDOSELENOPHOSPHATE-DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF Centrum Badan Molekularnych I Makromolekularnych Pan (PL) 2009-09-09 — — EP disclosed
US-20090098139-A1 Combination therapy for the treatment of neovascular disorders OLDTECH, INC. 2009-04-16 — — US disclosed
US-20090093432-A1 TUMOR INHIBITION BY MODULATING SPROUTY EXPRESSION OR ACTIVITY MICHIGAN STATE UNIVERSITY 2009-04-09 — — US disclosed
US-7514549-B2 Tumor inhibition by modulating sprouty expression or activity MICHIGAN STATE UNIVERSITY (US) 2009-04-07 — — US disclosed
US-20090088721-A1 Enhanced retinal delivery of a nucleic acid through iontophoresis EYEGATE PHARMA S.A.S. 2009-04-02 — — US disclosed
WO-2009005382-A3 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF CT BADAN MOLEKULAR I MAKRO (PL) 2009-03-05 — — WO disclosed
WO-2009005382-A2 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2009-01-08 — — WO disclosed
WO-2009005382-A2 DERIVATIVES OF NUCLEOSIDE-5'-O-HYPOPHOSPHATES AND THEIR MONO- AND DITHIOHYPOPHOSPHATE ANALOGUES AND THE PROCESS FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2009-01-08 — — WO disclosed
WO-2008125908-A2 ENHANCED RETINAL DELIVERY OF A NUCLEIC ACID THROUGH IONTOPHORESIS EYEGATE PHARMA S.A. (US) 2008-10-23 — — WO disclosed
WO-2008125116-A2 UPAR INHIBITION AARHUS UNIVERSITET (DK) 2008-10-23 — — WO disclosed
EP-1981520-A2 COMBINATION THERAPY FOR THE TREATMENT OF NEOVASCULAR DISORDERS (OSI) Eyetech, Inc. (US) 2008-10-22 — — EP disclosed
EP-1919930-A2 NEW NUCLEIC ACID BASE PAIRS Dako Denmark A/S (DK) 2008-05-14 — — EP disclosed
WO-2008048128-A1 5'-O-[(N-ACYL)AMIDOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDOTHIOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDODITHIOPHOSPHATE]- AND 5'-O-[(N- ACYL)AMIDOSELENOPHOSPHATE]-DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2008-04-24 — — WO disclosed
WO-2008048128-A1 5'-O-[(N-ACYL)AMIDOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDOTHIOPHOSPHATE]- AND 5'-O-[(N-ACYL)AMIDODITHIOPHOSPHATE]- AND 5'-O-[(N- ACYL)AMIDOSELENOPHOSPHATE]-DERIVATIVES OF NUCLEOSIDES AND PROCESSES FOR THE MANUFACTURE THEREOF CENTRUM BADAN MOLEKULARNYCH I MAKROMOLEKULARNYCH, POLSKIEJ AKADEMII NAUK (PL) 2008-04-24 — — WO disclosed
EP-1877433-A2 VEGF VARIANTS (OSI) EYETECH, INC. (US) 2008-01-16 — — EP disclosed
US-20070243548-A1 Calumenin-directed diagnostics and therapeutics for cancer and chemotherapeutic drug resistance AURELIUM BIOPHARMA INC. (CA) 2007-10-18 — — US disclosed
WO-2007087457-A2 COMBINATION THERAPY FOR THE TREATMENT OF NEOVASCULAR DISORDERS (OSI) EYETECH, INC. (US) 2007-08-02 — — WO disclosed
US-20070178476-A1 Detection of oligonucleotides by dual hybridization OLDTECH, INC. 2007-08-02 — — US disclosed
WO-2007072219-A2 ALPHA ENOLASE-DIRECTED DIAGNOSTICS AND THERAPEUTICS FOR CANCER AND CHEMOTHERAPEUTIC DRUG RESISTANCE AURELIUM BIOPHARMA INC. (US) 2007-06-28 — — WO disclosed
WO-2007072221-A2 SURFACE MARKER-DIRECTED CANCER THERAPEUTICS AURELIUM BIOPHARMA INC. (US) 2007-06-28 — — WO disclosed
US-20070122414-A1 Surface marker-directed cancer therapeutics AURELIUM BIOPHARMA INC. (CA) 2007-05-31 — — US disclosed
US-20070122830-A1 Prohibitin-directed diagnostics and therapeutics for cancer and chemotherapeutic drug resistance AURELIUM BIOPHARMA INC. (CA) 2007-05-31 — — US disclosed
WO-2007045998-A2 NEW NUCLEIC ACID BASE PAIRS DAKO DENMARK A/S (US) 2007-04-26 — — WO disclosed
EP-1776474-A2 DETECTION OF OLIGONULEOTIDES BY DUAL HYBRIDIZATION (OSI) EYETECH, INC. (US) 2007-04-25 — — EP disclosed
US-20070077583-A1 Alpha enolase-directed diagnostics and therapeutics for cancer and chemotherapeutic drug resistance AURELIUM BIOPHARMA, INC. (CA) 2007-04-05 — — US disclosed
US-20070066522-A1 Tumor inhibition by modulating sprouty expression or activity MICHIGAN STATE UNIVERSITY (US) 2007-03-22 — — US disclosed
EP-1737497-A2 NUCLEIC ACID APTAMERS CONJUGATED TO HIGH MOLECULAR WEIGHT STERIC GROUPS (OSI) EYETECH, INC. (US) 2007-01-03 — — EP disclosed
US-20060286636-A1 VEGF variants OLDTECH, INC. 2006-12-21 — — US disclosed
WO-2006119035-A2 VEGF VARIANTS (OSI) EYETECH, INC. (US) 2006-11-09 — — WO disclosed
WO-2006113579-A2 TUMOR INHIBITION BY MODULATING SPROUTY EXPRESSION OR ACTIVITY MICHIGAN STATE UNIVERSITY (US) 2006-10-26 — — WO disclosed
EP-1660057-A2 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS (OSI) EYETECH, INC. (US) 2006-05-31 — — EP disclosed
US-RE39112-E1 Purine derivatives and adenosine A2 receptor antagonists serving as preventives/remedies for diabetes EISAI CO., LTD. (JP) 2006-05-30 — — US disclosed
EP-1654362-A2 5'-AND 3'-CAPPED APTAMERS AND USES THEREFOR EYETECH PHARMACEUTICALS, INC. (US) 2006-05-10 — — EP disclosed
WO-2006012468-A2 DETECTION OF OLIGONULEOTIDES BY DUAL HYBRIDIZATION (OSI) EYETECH, INC. (US) 2006-02-02 — — WO disclosed
US-20050260153-A1 Facilitation of iontophoresis using charged moieties OLDTECH, INC. 2005-11-24 — — US disclosed
US-20050260651-A1 Enhanced biologically active conjugates OLDTECH, INC. 2005-11-24 — — US disclosed
WO-2005110489-A2 NUCLEIC ACID APTAMERS CONJUGATED TO HIGH MOLECULAR WEIGHT STERIC GROUPS (OSI) EYETECH, INC. (US) 2005-11-24 — — WO disclosed
EP-1221444-B1 FUSED IMIDAZOLE COMPOUNDS AND REMEDIES FOR DIABETES MELLITUS EISAI CO LTD (JP) 2005-08-31 — — EP disclosed
US-20050096257-A1 Administering platelet derived growth factor antagonist and endothelial growth factor antagonist OPHTHOTECH CORPORATION 2005-05-05 — — US disclosed
US-20050096290-A1 5'-and 3'-capped aptamers and uses therefor (OSI) EYETECH, INC. 2005-05-05 — — US disclosed
WO-2005020972-A2 COMBINATION THERAPY FOR THE TREATMENT OF OCULAR NEOVASCULAR DISORDERS (OSI) EYETECH, INC. (US) 2005-03-10 — — WO disclosed
WO-2005014814-A2 5’-AND 3’-CAPPED APTAMERS AND USES THEREFOR (OSI) EYETECH, INC. (US) 2005-02-17 — — WO disclosed
US-6841549-B1 Condensed imidazole compounds and a therapeutic agent for diabetes mellitus EISAI CO., LTD. (JP) 2005-01-11 — — US disclosed
US-20040214198-A1 Allele-targeted RNA interference UNIVERSITY OF MASSACHUSETTS 2004-10-28 — — US disclosed
CN-1166666-C Fused imiazole compounds and remedies for diabetes mellitus ������������ʽ���� 2004-09-15 — — CN disclosed
WO-2004046324-A2 ALLELE-TARGETED RNA INTERFERENCE UNIVERSITY OF MASSACHUSETTS (US) 2004-06-03 — — WO disclosed
US-6579868-B1 Reacting a 2,6-dihalo-substituted purine compound with ammonia or an amine EISAI CO., LTD. (JP) 2003-06-17 — — US disclosed
EP-1054012-B1 PURINE DERIVATIVES AND ADENOSINE A2 RECEPTOR ANTAGONISTS SERVING AS PREVENTIVES/REMEDIES FOR DIABETES EISAI CO LTD (JP) 2003-06-11 — — EP disclosed
EP-1300147-A1 Purine compounds and adenosine A2 receptor antagonist as preventive or therapeutic agent for diabetes mellitus Eisai Co. Ltd (JP) 2003-04-09 — — EP disclosed
CN-1365361-A Condensed imidazole compound and drug for treating diabetes EISAI CO LTD (JP) 2002-08-21 — — CN disclosed
EP-1221444-A1 FUSED IMIDAZOLE COMPOUNDS AND REMEDIES FOR DIABETES MELLITUS Eisai Co., Ltd. (JP) 2002-07-10 — — EP disclosed
EP-1054012-A1 PURINE DERIVATIVES AND ADENOSINE A2 RECEPTOR ANTAGONISTS SERVING AS PREVENTIVES/REMEDIES FOR DIABETES Eisai Co., Ltd. (JP) 2000-11-22 — — EP disclosed
EP-1054012-A1 PURINE DERIVATIVES AND ADENOSINE A2 RECEPTOR ANTAGONISTS SERVING AS PREVENTIVES/REMEDIES FOR DIABETES Eisai Co., Ltd. (JP) 2000-11-22 — — EP 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 (28 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-20210252036-A1 METHODS OF TREATING CANCER BY INHIBITING UBIQUITIN CONJUGATING ENZYME E2 K (UBE2K) UBE2G2, UBE2N, UBE2E1 PDPK1 1234/4885GDA 2663/4885CDK2 154/4885
US-11001891-B2 Methods for treating Parkinson's disease SNCA, GBA3, LRRK2 PDPK1 283/4885GDA 30/4885CDK2 3133/4885
US-20170166891-A1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA HSP90AB1, HSP90AB2P, HSP90AA1 PDPK1 586/4885GDA 3493/4885CDK2 3504/4885
US-20160354492-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20140303112-A1 Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) PRKAG2, PRKAB2, PRKAG1 PDPK1 281/4885GDA 1170/4885CDK2 1757/4885
US-20160304552-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20140179621-A1 Methods for Treating or Preventing Ophthalmological Diseases VEGFA, PDGFA, PGF PDPK1 3318/4885GDA 1417/4885CDK2 2854/4885
US-20160348099-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20170136132-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, RNGTT, NSUN3 PDPK1 3868/4885GDA 83/4885CDK2 4020/4885
US-20190255194-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, RNGTT, NSUN3 PDPK1 3868/4885GDA 83/4885CDK2 4020/4885
US-20150353930-A1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA HSP90AB1, HSP90AB2P, HSP90AA1 PDPK1 736/4885GDA 2959/4885CDK2 3727/4885
US-20160354490-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20240165267-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20160354491-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20090088721-A1 Enhanced retinal delivery of a nucleic acid through iontophoresis NR2E3, MITF, SLC5A11 PDPK1 3931/4885GDA 1043/4885CDK2 3386/4885
US-10023864-B2 Methods of treating a metabolic syndrome by modulating heat shock protein (HSP) 90-beta HSP90AB1, HSP90AB2P, HSP90AA1 PDPK1 736/4885GDA 2959/4885CDK2 3727/4885
US-20050096290-A1 5'-and 3'-capped aptamers and uses therefor FLT4, TEK, FLT1 PDPK1 4252/4885GDA 314/4885CDK2 2868/4885
US-20170175129-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, RNGTT, NSUN3 PDPK1 3868/4885GDA 83/4885CDK2 4020/4885
US-20170136131-A1 ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, RNGTT, NSUN3 PDPK1 3868/4885GDA 83/4885CDK2 4020/4885
US-20220064732-A1 METHODS FOR TREATING PARKINSON'S DISEASE SNCA, GBA3, LRRK2 PDPK1 283/4885GDA 30/4885CDK2 3133/4885
US-20160354493-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20160264969-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES VEGFA, PDGFA, PGF PDPK1 3318/4885GDA 1417/4885CDK2 2854/4885
US-10286086-B2 Alternative nucleic acid molecules and uses thereof NSUN2, RNGTT, NSUN3 PDPK1 3868/4885GDA 83/4885CDK2 4020/4885
US-20150307542-A1 MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF NSUN2, ADAR, NSUN3 PDPK1 3533/4885GDA 36/4885CDK2 3750/4885
US-20120184569-A1 A3 ADENOSINE RECEPTOR AGONISTS AND ANTAGONISTS ADORA3, ADORA1, ADORA2A PDPK1 2789/4885GDA 353/4885CDK2 1677/4885
US-20050260153-A1 Facilitation of iontophoresis using charged moieties ANXA11, SLC7A1, TRPC6 PDPK1 4234/4885GDA 1634/4885CDK2 4040/4885
US-20180135129-A1 METHODS FOR TREATING PARKINSON'S DISEASE SNCA, GBA3, LRRK2 PDPK1 283/4885GDA 30/4885CDK2 3133/4885
US-20140154266-A1 METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA HSP90AB1, HSP90AB2P, HSP90AA1 PDPK1 586/4885GDA 3493/4885CDK2 3504/4885

“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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