Draflazine

Draflazine

SCHEMBL215826

NC(=O)C1CN(CCCCC(c2ccc(F)cc2)c2ccc(F)cc2)CCN1CC(=O)Nc1c(Cl)cc(N)cc1Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC29A1 Q99808 2/20 1.00
KCNH2 Q12809 11/20 0.49
SLC6A3 Q01959 6/20 0.49
HTR2A P28223 4/20 0.49
DRD3 P35462 4/20 0.49
OPRK1 P41145 4/20 0.49
OPRD1 P41143 3/20 0.49
DRD2 P14416 3/20 0.49
ADORA3 P0DMS8 3/20 0.49
ADRA1A P35348 3/20 0.49
HRH1 P35367 3/20 0.49
CYP3A4 P08684 2/20 0.49
CYP2D6 P10635 2/20 0.49
MEN1 O00255 2/20 0.49
KMT2A Q03164 2/20 0.49
SLC6A2 P23975 2/20 0.49
SLC6A4 P31645 2/20 0.49
HTR2B P41595 2/20 0.49
MLNR O43193 1/20 0.49
NR1I2 O75469 1/20 0.49

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
Draflazine SCHEMBL7705425 1.00 SLC29A1 (1.00) SLC29A1KCNH2SLC6A3HTR2ADRD3
Draflazine SCHEMBL9362256 0.99 SLC29A1 (0.98) SLC29A1KCNH2SLC6A3HTR2ADRD3
Draflazine SCHEMBL9410932 0.99 SLC29A1 (0.98) SLC29A1KCNH2SLC6A3HTR2ADRD3
Hydrochloric Acid SCHEMBL9808242 0.93 SLC29A1 (0.86) SLC29A1KCNH2SLC6A3HTR2ADRD3
SCHEMBL10458587 0.92 SLC29A1 (0.85) SLC29A1KCNH2SLC6A3HTR2ADRD3
SCHEMBL10460454 0.92 SLC29A1 (0.85) SLC29A1KCNH2SLC6A3HTR2ADRD3
SCHEMBL9808240 0.91 SLC29A1 (0.84) SLC29A1KCNH2SLC6A3HTR2ADRD3
SCHEMBL10458592 0.91 SLC29A1 (0.84) SLC29A1KCNH2SLC6A3HTR2ADRD3
SCHEMBL9808247 0.90 SLC29A1 (0.82) SLC29A1KCNH2SLC6A3HTR2ADRD3
SCHEMBL10460327 0.90 SLC29A1 (0.82) SLC29A1KCNH2SLC6A3HTR2ADRD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025074343-A2 PRODRUGS OF HUMAN DIHYDROOROTATE DEHYDROGENASE (hDHODH) INHIBITORS DRUG DISCOVERY AND CLINIC S.R.L. (IT) 2025-04-10 WO claimed
US-20230414575-A1 MK2 ACTIVATING COMPOUNDS FOR USE IN TREATING VASCULAR LEAK AND ENDOTHELIAL BARRIER DISORDERS AKTTYVA THERAPEUTICS INC (US) 2023-12-28 US claimed
EP-4244341-A2 MK2 ACTIVATING COMPOUNDS FOR USE IN TREATING VASCULAR LEAK AND ENDOTHELIAL BARRIER DISORDERS Akttyva Therapeutics, Inc. (US) 2023-09-20 EP claimed
WO-2022104097-A2 MK2 ACTIVATING COMPOUNDS FOR USE IN TREATING VASCULAR LEAK AND ENDOTHELIAL BARRIER DISORDERS AKTTYVA THERAPEUTICS, INC. (US) 2022-05-19 WO claimed
EP-2459227-B1 Prodrugs containing an aromatic amine connected by an amide bond to a carrier ASCENDIS PHARMA AS (DK) 2021-03-17 EP claimed
CN-110214009-A Dipyridamole is for treating SLC29A2 core-expression cancer 中央研究院 2019-09-06 CN claimed
US-9173953-B2 Prodrugs containing an aromatic amine connected by an amido bond to a linker ASCENDIS PHARMA AS (DK) 2015-11-03 US claimed
US-9016221-B2 Surface topographies for non-toxic bioadhesion control UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. (US) 2015-04-28 US claimed
US-20120156260-A1 Prodrugs Containing an Aromatic Amine Connected By an Amido Bond to a Linker ASCENDIS PHARMA A/S (DK) 2012-06-21 US claimed
EP-2459227-A1 PRODRUGS CONTAINING AN AROMATIC AMINE CONNECTED BY AN AMIDO BOND TO A LINKER Ascendis Pharma A/S (DK) 2012-06-06 EP claimed
US-6403589-B1 NUCLEOSIDE TRANSPORT INHIBITOR JANSSEN PHARMACEUTICA N.V. (BE) 2002-06-11 US claimed
EP-0999840-A1 USE OF DRAFLAZINE-ANALOGUES FOR TREATING PAIN JANSSEN PHARMACEUTICA N.V. (BE) 2000-05-17 EP claimed
EP-0814810-A4 ADENOSINE AS A POSITIVE INOTROP IN THE COMPROMISED HEART UNIV MASSACHUSETTS MEDICAL (US) 1999-06-09 EP claimed
WO-1998057643-A1 USE OF DRAFLAZINE-ANALOGUES FOR TREATING PAIN JANSSEN PHARMACEUTICA N.V. (BE) 1998-12-23 WO claimed
WO-1998019540-A1 IN VIVO SELECTION OF PRIMITIVE HEMATOPOIETIC CELLS SAINT JUDE CHILDREN'S RESEARCH HOSPITAL (US) 1998-05-14 WO claimed
EP-0814810-A1 ADENOSINE AS A POSITIVE INOTROP IN THE COMPROMISED HEART UNIVERSITY OF MASSACHUSETTS MEDICAL CENTER (US) 1998-01-07 EP claimed
US-5629298-A INCREASING CONTRACTILE PERFORMANCE, ADENOSINE TRANSPORT INHIBITORS USED AS POTENTIATORS UNIVERSITY OF MASSACHUSETTS MEDICAL CENTER (US) 1997-05-13 US claimed
WO-1996028163-A1 ADENOSINE AS A POSITIVE INOTROP IN THE COMPROMISED HEART UNIVERSITY OF MASSACHUSETTS MEDICAL CENTER (US) 1996-09-19 WO claimed
EP-0577171-A2 Use of piperazine acetamide derivatives against reperfusion damage JANSSEN PHARMACEUTICA N.V. (BE) 1994-01-05 EP claimed
WO-1991007967-A2 METHOD OF PREVENTING OR LIMITING REPERFUSION DAMAGE JANSSEN PHARMACEUTICA N.V. (BE) 1991-06-13 WO 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 (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-20120156260-A1 Prodrugs Containing an Aromatic Amine Connected By an Amido Bond to a Linker DAO, DNPEP, DDC SLC29A1 98/4885KCNH2 1891/4885SLC6A3 114/4885

“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.