SCHEMBL7789108

SCHEMBL7789108

O=C1c2cc3ccccc3nc2C=CC1Nc1ccccc1

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ RAB9A P51151 5/20 0.38
▸ NPC1 O15118 4/20 0.38
▸ NFKB1 P19838 2/20 0.35
▸ NFKB2 Q00653 2/20 0.35
▸ RELA Q04206 2/20 0.35
▸ ALDH1A1 P00352 5/20 0.34
▸ HPGD P15428 3/20 0.34
▸ MAPT P10636 2/20 0.34
▸ GLA P06280 2/20 0.34
▸ ACHE P22303 1/20 0.34
▸ SMN1; SMN2 Q16637 3/20 0.34
▸ KMT2A Q03164 3/20 0.34
▸ PDE2A O00408 2/20 0.34
▸ PDE3B Q13370 2/20 0.34
▸ PDE3A Q14432 2/20 0.34
▸ MEN1 O00255 1/20 0.34
▸ TP53 P04637 1/20 0.34
▸ CYP3A4 P08684 1/20 0.34
▸ MAPK1 P28482 1/20 0.34
▸ HIF1A Q16665 1/20 0.34

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
SCHEMBL9334583 0.84 NPC1 (0.41) RAB9ANPC1ALDH1A1HPGDMAPT
SCHEMBL11799791 0.81 NPC1 (0.36) RAB9ANPC1ALDH1A1HPGDMAPT
SCHEMBL6743467 0.80 TOP2A (0.40) RAB9ANPC1ALDH1A1MAPTSMN1; SMN2
SCHEMBL18493250 0.79 RAB9A (0.35) RAB9ANPC1ALDH1A1MAPTSMN1; SMN2
SCHEMBL16346102 0.77 NPC1 (0.40) RAB9ANPC1ALDH1A1HPGDMAPT
SCHEMBL9501858 0.77 PDE3B (0.40) RAB9ANPC1ALDH1A1MAPTSMN1; SMN2
SCHEMBL7088775 0.77 NPC1 (0.41) RAB9ANPC1ALDH1A1HPGDMAPT
SCHEMBL3735368 0.77 RAB9A (0.45) RAB9ANPC1ALDH1A1HPGDMAPT
SCHEMBL3234460 0.77 NPC1 (0.41) RAB9ANPC1ALDH1A1HPGDMAPT
SCHEMBL9690618 0.77 NPC1 (0.41) RAB9ANPC1ALDH1A1HPGDMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0877021-B1 Process for preparing 2-anilinoacridones CIBA SC HOLDING AG (CH) 2001-05-09 — — EP claimed
EP-0696620-B1 Solid solutions of pyrrolo- 3,4-c -pyrroles with quinacridonequinones CIBA SC HOLDING AG (CH) 2000-04-26 — — EP claimed
US-6022970-A Process for preparing 2-anilinoacridones CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-02-08 — — US claimed
CN-1199046-A Process for preparing 2-anilinoacridones CIBA GEIGY AG (CH) 1998-11-18 — — CN claimed
EP-0877021-A1 Process for preparing 2-anilinoacridones Ciba SC Holding AG (CH) 1998-11-11 — — EP claimed
EP-0696620-A1 Solid solutions of pyrrolo- 3,4-c -pyrroles with quinacridonequinones CIBA-GEIGY AG (CH) 1996-02-14 — — EP claimed
US-5472496-A Ternery component; light and weatherfastness; useful as colorant in plastics, inks and automotive paints CIBA-GEIGY CORPORATION (US) 1995-12-05 — — US claimed
EP-0069396-B1 PREPARATION OF PIGMENTARY FORM OF QUINACRIDONE PIGMENTS CIBA-GEIGY AG (CH) 1986-03-12 — — EP claimed
US-4455173-A Preparation of pigmentary form of quinacridone pigments E. I. DU PONT DE NEMOURS AND COMPANY (US) 1984-06-19 — — US claimed
EP-0012432-B1 LIGHT-STABLE QUINACRIDONEQUINONE YELLOW PIGMENT AND POST TREATMENT TO IMPROVE ITS DISPERSIBILITY E.I. DU PONT DE NEMOURS AND COMPANY (US) 1983-01-26 — — EP claimed
EP-0069396-A2 Preparation of pigmentary form of quinacridone pigments CIBA-GEIGY AG (CH) 1983-01-12 — — EP claimed
US-4286998-A CONTAINING 2-ANILINOACRIDONE, 5,6,7,8-TETRAHYDRO-2-ANALINOACRIDONE, 6-ANILINOQUINOLONE OR 2-AMINOACRIDONE AS A STABILIZER E. I. DUPONT DE NEMOURS AND COMPANY (US) 1981-09-01 — — US claimed
EP-0012432-A1 Light-stable quinacridonequinone yellow pigment and post treatment to improve its dispersibility E.I. DU PONT DE NEMOURS AND COMPANY (US) 1980-06-25 — — EP claimed
JP-10338674-A — — None — — JP disclosed
EP-0790281-B1 Pigment compositions CIBA SC HOLDING AG (CH) 2001-12-05 — — EP disclosed
EP-0877021-B1 Process for preparing 2-anilinoacridones CIBA SC HOLDING AG (CH) 2001-05-09 — — EP disclosed
EP-0028445-A2 Acridinones, their preparation and use; intermediates and their preparation CIBA-GEIGY AG (CH) 1981-05-13 — — EP disclosed
US-4258190-A BY REACTING CYCLOHEXANONE AND AN OXALATE ESTER TO FORM A CYCLOHEXANONECARBOXYLATE INTERMEDIATE E. I. DU PONT DE NEMOURS AND COMPANY (US) 1981-03-24 — — US disclosed
EP-0012432-A1 Light-stable quinacridonequinone yellow pigment and post treatment to improve its dispersibility E.I. DU PONT DE NEMOURS AND COMPANY (US) 1980-06-25 — — EP disclosed
EP-0012432-A1 Light-stable quinacridonequinone yellow pigment and post treatment to improve its dispersibility E.I. DU PONT DE NEMOURS AND COMPANY (US) 1980-06-25 — — EP disclosed
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