SCHEMBL504178

SCHEMBL504178

CCN(Cl)C(=O)N(N=O)C1CCCCC1

nearest known ligand 0.37

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ADH1A P07327 2/20 0.37
ADH1C P00326 1/20 0.37
NPSR1 Q6W5P4 3/20 0.35
ADRA2A P08913 1/20 0.33
PDE4A P27815 1/20 0.33
ADRA1A P35348 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
ALDH1A1 P00352 2/20 0.32
LMNA P02545 2/20 0.32
TSHR P16473 2/20 0.32
S1PR1 P21453 2/20 0.31
S1PR3 Q99500 2/20 0.31
XBP1 P17861 1/20 0.31
NPC1 O15118 1/20 0.30
RAB9A P51151 1/20 0.30
FDPS P14324 1/20 0.30

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
SCHEMBL11113407 0.79 ADH1A (0.41) ADH1AADH1CNPSR1L3MBTL1MEN1
SCHEMBL1902755 0.75 ADRA2A (0.42) ADH1AADH1CNPSR1ADRA2APDE4A
SCHEMBL14776360 0.74 ADH1C (0.35) ADH1AADH1CNPSR1MEN1KMT2A
SCHEMBL701945 0.73 ADRA2A (0.40) ADH1AADH1CNPSR1ADRA2APDE4A
SCHEMBL102987 0.72 LMNA (0.36) ADH1AADH1CNPSR1ADRA2APDE4A
SCHEMBL1902754 0.72 ADH1C (0.33) ADH1AADH1CALDH1A1TSHRS1PR1
SCHEMBL6467646 0.71 EPHX1 (0.42) ADH1AADH1CADRA2APDE4AADRA1A
SCHEMBL14791027 0.70 LMNA (0.37) ADH1AADH1CNPSR1ADRA2APDE4A
SCHEMBL1238560 0.69 ALOX5 (0.39) ADH1AADH1CADRA2APDE4AADRA1A
SCHEMBL39462 0.68 ADRA2A (0.40) ADH1AADH1CADRA2APDE4AADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2673362-B1 PLEXIN-B1 ANTAGONISTS AND USES THEREOF Ruprecht-Karls-Universität Heidelberg (DE) 2017-06-07 EP claimed
CN-114558032-A Method for preparing platelets from pluripotent stem cells and composition thereof 安斯泰来再生医药协会 2022-05-31 CN disclosed
CN-105101979-B Method for preparing platelets from pluripotent stem cells and composition thereof 安斯泰来再生医药协会 2021-10-08 CN disclosed
EP-3191114-B1 OCCIDIOFUNGIN FORMULATIONS AND USES THEREOF UNIV MISSISSIPPI STATE (US) 2021-03-03 EP disclosed
US-10265374-B2 Occidiofungin formations and uses thereof MISSISSIPPI STATE UNIVERSITY (US) 2019-04-23 US disclosed
US-20170281721-A1 OCCIDIOFUNGIN FORMATIONS AND USES THEREOF MISSISSIPPI STATE UNIVERSITY (US) 2017-10-05 US disclosed
EP-3191114-A1 OCCIDIOFUNGIN FORMULATIONS AND USES THEREOF Smith, James (US) 2017-07-19 EP disclosed
WO-2016040940-A1 OCCIDIOFUNGIN FORMULATIONS AND USES THEREOF AUSTIN, FRANK (US) 2016-03-17 WO disclosed
US-8476246-B2 Combination of a chemotherapeutic agent and an inhibitor of the TGF-beta system ANTISENSE PHARMA GMBH (DE) 2013-07-02 US disclosed
US-20120142722-A1 CONJUGATES OF CYTOTOXIC DRUGS APOSENSE LTD. (IL) 2012-06-07 US disclosed
US-6949350-B1 Chemosensitivity determination using phosphatidylserine EVOTEC ANALYTICAL SYSTEMS GMBH (DE) 2005-09-27 US disclosed
US-20050203082-A1 Combination therapy with inhibitors of inducible nitric oxide synthase and alkylating agents PHARMACIA CORPORATION 2005-09-15 US disclosed
WO-2005059133-A2 COMBINATION THERAPY ASSOCIATING A TGF-BRETA ANTAGONIST WITH A CHEMIOTHERAPEUTIC AGENT ANTISENSE PHARMA GMBH (DE) 2005-06-30 WO disclosed
WO-2005025620-A2 COMBINATION THERAPY WITH INHIBITORS OF INDUCIBLE NITRIC OXIDE SYNTHASE AND ALKYLATING AGENTS PHARMACIA CORPORATION (US) 2005-03-24 WO disclosed
US-5736129-A Flow cytometric pharmacosensitivity assay and method of cancer treatment SHAKER CORPORATION, A DELAWARE CORPORATION 1998-04-07 US disclosed
WO-1997019189-A1 FLOW CYTOMETRIC PHARMACOSENSITIVITY ASSAY AND METHOD OF CANCER TREATMENT MEDENICA RAJKO D (US) 1997-05-29 WO disclosed
EP-0525188-B1 LIPOSOME COMPOSITION TAKEDA CHEMICAL INDUSTRIES LTD (JP) 1995-03-01 EP disclosed
US-5252336-A Good dispersibility; high stability; high encapsulation properties TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1993-10-12 US disclosed
EP-0525188-A1 LIPOSOME COMPOSITION. TAKEDA CHEMICAL INDUSTRIES LTD (JP) 1993-02-03 EP disclosed
WO-1991016040-A1 LIPOSOME COMPOSITION TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1991-10-31 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-20050203082-A1 Combination therapy with inhibitors of inducible nitric oxide synthase and alkylating agents NOS2, NOS1, NOS3 ADH1A 1360/4885ADH1C 1600/4885NPSR1 3888/4885
US-20120142722-A1 CONJUGATES OF CYTOTOXIC DRUGS CD47, MCL1, BAD ADH1A 4313/4885ADH1C 4328/4885NPSR1 3013/4885

“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.