Dyrene

Dyrene

SCHEMBL6579552

Clc1nc(Cl)nc(Nc2ccccc2Cl)n1.NC(=O)O.NC(=O)O.NC(=O)O

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 1/20 0.77
▸ NFKB1 P19838 1/20 0.51
▸ SMN1; SMN2 Q16637 2/20 0.51
▸ HDAC3 O15379 1/20 0.49
▸ HDAC1 Q13547 1/20 0.49
▸ HDAC2 Q92769 1/20 0.49
▸ HDAC6 Q9UBN7 1/20 0.49
▸ MAPT P10636 3/20 0.47
▸ KMT2A Q03164 2/20 0.47
▸ MEN1 O00255 1/20 0.47
▸ MAPK1 P28482 1/20 0.47
▸ KDM4E B2RXH2 2/20 0.46
▸ ALDH1A1 P00352 1/20 0.46
▸ CXCL8 P10145 1/20 0.46
▸ AURKA O14965 3/20 0.46
▸ AURKB Q96GD4 2/20 0.46
▸ ULK1 O75385 1/20 0.46
▸ RAD52 P43351 1/20 0.46
▸ CYP1A2 P05177 1/20 0.45
▸ NPC1 O15118 1/20 0.43

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
Dyrene SCHEMBL2342691 1.00 TSHR (0.77) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL10874656 0.95 TSHR (0.80) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL11744896 0.92 TSHR (0.75) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL14060904 0.89 TSHR (0.65) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL5391750 0.88 TSHR (0.92) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL1293204 0.88 TSHR (0.92) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL8166670 0.88 TSHR (1.00) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL13280 0.88 TSHR (1.00) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL1903290 0.88 TSHR (1.00) TSHRNFKB1SMN1; SMN2HDAC3HDAC1
Dyrene SCHEMBL29364667 0.88 TSHR (1.00) TSHRNFKB1SMN1; SMN2HDAC3HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0604922-B1 Durable compositions and use of same CYTEC TECH CORP (US) 2004-11-17 — — EP claimed
EP-0604922-A1 Durable compositions and use of same CYTEC TECHNOLOGY CORP. (US) 1994-07-06 — — EP claimed
EP-0604922-B1 Durable compositions and use of same CYTEC TECH CORP (US) 2004-11-17 — — EP disclosed
EP-0930303-B1 A process for preparing isocyanate compounds from haloaminotriazines and acid halides CYTEC TECH CORP (US) 2004-02-04 — — EP disclosed
EP-0933371-B1 N-halo acid amides CYTEC TECH CORP (US) 2003-04-09 — — EP disclosed
EP-0565774-B1 Process for preparing amide derivatives from halominotriazines and acid halides CYTEC TECH CORP (US) 2001-03-28 — — EP disclosed
US-6121446-A Preparation of tris-substituted alkoxycarbonylamino-1,3,5-triazine compounds CYTEC TECHNOLOGY CORPORATION 2000-09-19 — — US disclosed
EP-0933369-A1 Tris-(omega-haloacyl)melamines CYTEC TECHNOLOGY CORP. (US) 1999-08-04 — — EP disclosed
EP-0933370-A1 Tris-(2,2,6,6-tetramethyl-piperid-4-yl-aminocarbonyl)melamine CYTEC TECHNOLOGY CORP. (US) 1999-08-04 — — EP disclosed
EP-0933371-A1 N-halo acid amides CYTEC TECHNOLOGY CORP. (US) 1999-08-04 — — EP disclosed
EP-0930303-A2 A process for preparing isocyanate compounds from haloaminotriazines and acid halides CYTEC TECHNOLOGY CORP. (US) 1999-07-21 — — EP disclosed
US-5593735-A Aminoresin based coatings containing 1,3,5-triazine tris-carbamate co-crosslinkers CYTEC TECHNOLOGY CORP. (US) 1997-01-14 — — US disclosed
US-5574103-A ETCH RESISTANCE, NO FORMALDEHYDE CYTEC TECHNOLOGY CORP. (US) 1996-11-12 — — US disclosed
US-5574103-A ETCH RESISTANCE, NO FORMALDEHYDE CYTEC TECHNOLOGY CORP. (US) 1996-11-12 — — US disclosed
US-5571915-A Process for preparing amide derivatives from haloaminotriazines and acid halides CYTEC TECHNOLOGY CORP. (US) 1996-11-05 — — US disclosed
US-5405959-A Haloaminotraizines and acid halides CYTEC TECHNOLOGY CORP. (US) 1995-04-11 — — US disclosed
EP-0604922-A1 Durable compositions and use of same CYTEC TECHNOLOGY CORP. (US) 1994-07-06 — — EP disclosed
US-5288865-A Process for preparing amide derivatives from haloaminotriazines and acid halides AMERICAN CYANAMID COMPANY (US) 1994-02-22 — — US disclosed
EP-0565774-A2 Process for preparing amide derivatives from halominotriazines and acid halides CYTEC TECHNOLOGY CORP. (US) 1993-10-20 — — EP disclosed
EP-0541966-A2 Process for preparing amide derivatives from halomines and acid halides AMERICAN CYANAMID COMPANY (US) 1993-05-19 — — EP disclosed
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