SCHEMBL7077073

SCHEMBL7077073

C=CCc1ccc([N+](=O)[O-])cc1Cl

nearest known ligand 0.55

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ HSD17B10 Q99714 1/20 0.55
▸ KMT2A Q03164 3/20 0.49
▸ ALDH1A1 P00352 4/20 0.44
▸ VCAM1 P19320 1/20 0.42
▸ PDE7A Q13946 4/20 0.42
▸ MEN1 O00255 1/20 0.41
▸ POLB P06746 1/20 0.41
▸ MAPT P10636 1/20 0.41
▸ TDP1 Q9NUW8 1/20 0.41
▸ CYP1A2 P05177 1/20 0.41
▸ LMNA P02545 1/20 0.40
▸ SMN1; SMN2 Q16637 1/20 0.40
▸ PDE4B Q07343 1/20 0.40
▸ PDE4D Q08499 1/20 0.40
▸ PDE7B Q9NP56 1/20 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
SCHEMBL27401907 0.87 HSD17B10 (0.55) HSD17B10KMT2AALDH1A1VCAM1MEN1
SCHEMBL30714466 0.85 HSD17B10 (0.56) HSD17B10KMT2AALDH1A1VCAM1PDE7A
SCHEMBL1195412 0.85 HSD17B10 (0.56) HSD17B10KMT2AALDH1A1VCAM1PDE7A
SCHEMBL11097917 0.82 TSHR (0.44) HSD17B10KMT2AALDH1A1MEN1POLB
SCHEMBL30496244 0.81 CYP1A2 (0.57) KMT2AALDH1A1MEN1POLBMAPT
SCHEMBL1644916 0.81 CYP3A4 (0.51) KMT2AALDH1A1MEN1POLBMAPT
SCHEMBL7080582 0.81 CYP1A2 (0.57) KMT2AALDH1A1MEN1POLBMAPT
SCHEMBL28978217 0.81 HSD17B10 (0.60) HSD17B10KMT2AALDH1A1VCAM1PDE7A
SCHEMBL3161586 0.80 GPR35 (0.51) KMT2AALDH1A1MEN1POLBTDP1
SCHEMBL17182634 0.80 ALDH1A1 (0.47) HSD17B10KMT2AALDH1A1MEN1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0399293-B1 PROCESS FOR PREPARING 2-CHLORO-4-NITRO-ALKYLBENZENE BAYER AG (DE) 1993-09-01 — — EP claimed
US-5095157-A Friedel-crafts catalyst BAYER AKTIENGESELLSCHAFT (DE) 1992-03-10 — — US claimed
EP-1013636-B1 Preparation of allylic aromatic compounds AMERSHAM HEALTH AS (NO) 2003-07-09 — — EP disclosed
US-6284894-B1 AROMATIC AMINE IS REACTED FIRST WITH A NITRITE AND THEN WITH AN ALLYLIC OLEFIN HAVING AN ELIMINATABLE TERMINAL SUBSTITUENT. NYCOMED IMAGING AS (NO) 2001-09-04 — — US disclosed
US-6255542-B1 RING CHLORINATING 4-NITROALKYLBENZENE WITH CHLORINE OR CHLORING-RELEASING AGENT IN A LIQUID PHASE AND IN THE PRESENCE OF A FRIEDEL-CRAFTS CATALYST AND A DIARYL SULFIDE CO-CATALYST BAYER AKTIENGESELLSCHAFT (DE) 2001-07-03 — — US disclosed
US-6255542-B1 RING CHLORINATING 4-NITROALKYLBENZENE WITH CHLORINE OR CHLORING-RELEASING AGENT IN A LIQUID PHASE AND IN THE PRESENCE OF A FRIEDEL-CRAFTS CATALYST AND A DIARYL SULFIDE CO-CATALYST BAYER AKTIENGESELLSCHAFT (DE) 2001-07-03 — — US disclosed
US-6255542-B1 RING CHLORINATING 4-NITROALKYLBENZENE WITH CHLORINE OR CHLORING-RELEASING AGENT IN A LIQUID PHASE AND IN THE PRESENCE OF A FRIEDEL-CRAFTS CATALYST AND A DIARYL SULFIDE CO-CATALYST BAYER AKTIENGESELLSCHAFT (DE) 2001-07-03 — — US disclosed
JP-2001089422-A PRODUCTION OF 2-CHLORO-4-NITROALKYLBENZENE BAYER AG 2001-04-03 — — JP disclosed
CN-1286244-A Method for preparing 2-chloro-4-nitroalkylbenzene BAYER AG (DE) 2001-03-07 — — CN disclosed
EP-1078914-A1 Process for the preparation of 2-chloro-4-nitroalkylbenzene BAYER AG (DE) 2001-02-28 — — EP disclosed
EP-1013636-A1 Preparation of allylic aromatic compounds NYCOMED IMAGING AS (NO) 2000-06-28 — — EP disclosed
US-5095157-A Friedel-crafts catalyst BAYER AKTIENGESELLSCHAFT (DE) 1992-03-10 — — US disclosed
US-5095157-A Friedel-crafts catalyst BAYER AKTIENGESELLSCHAFT (DE) 1992-03-10 — — US disclosed
EP-0399293-A1 Process for preparing 2-chloro-4-nitro-alkylbenzene BAYER AG (DE) 1990-11-28 — — EP disclosed
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