SCHEMBL1003285

SCHEMBL1003285

Cc1cccc(P(=O)(c2cccc(C)c2)c2cccc(C)c2)c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 5/20 0.52
HPGD P15428 1/20 0.42
ALDH1A1 P00352 1/20 0.42
MAPK1 P28482 1/20 0.42
HDAC8 Q9BY41 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
NPC1 O15118 3/20 0.41
CASP3 P42574 1/20 0.41
SENP8 Q96LD8 1/20 0.41
SENP7 Q9BQF6 1/20 0.41
SENP6 Q9GZR1 1/20 0.41
ACP3 P15309 1/20 0.41
PARP1 P09874 1/20 0.40
TSHR P16473 1/20 0.40
RAB9A P51151 2/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.39
TP53 P04637 1/20 0.39

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
SCHEMBL29968470 1.00 ACHE (0.52) ACHEHPGDALDH1A1MAPK1HDAC8
SCHEMBL14339300 0.95 ACHE (0.48) ACHEHPGDALDH1A1MAPK1HDAC8
SCHEMBL4400932 0.93 ACHE (0.46) ACHEHPGDNPC1ACP3TSHR
SCHEMBL260337 0.93 ACHE (0.46) ACHEHPGDNPC1ACP3TSHR
SCHEMBL31212643 0.93 ACHE (0.46) ACHEHPGDNPC1ACP3TSHR
SCHEMBL31212639 0.93 ACHE (0.46) ACHEHPGDNPC1ACP3TSHR
SCHEMBL18780696 0.86 HSD17B1 (0.43) ACHEHPGDMEN1KMT2ALMNA
SCHEMBL3893074 0.83 ACHE (0.50) ACHEHPGDALDH1A1MAPK1HDAC8
SCHEMBL14072818 0.82 ACHE (0.39) ACHEHPGDMAPK1HDAC8HDAC6
SCHEMBL3355826 0.81 CA2 (0.52) ACHEHDAC8HDAC6NPC1CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12100809-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2024-09-24 US disclosed
US-20240301210-A1 FLUORINATED PHTHALOCYANINE COMPOUND, COLORING COMPOSITION, AND INKJET INK FUJIFILM CORPORATION (JP) 2024-09-12 US disclosed
CN-113698431-B Synthesis method of phosphine (III) compound 海南大学 2023-07-25 CN disclosed
CN-115055207-B Method for preparing aryl phosphine by reducing aryl phosphine oxide 清华大学 2023-07-21 CN disclosed
WO-2023136027-A1 FLUORINATED PHTHALOCYANINE COMPOUND, COLORING COMPOSITION, AND INKJET INK 富士フイルム株式会社 2023-07-20 WO disclosed
WO-2023090221-A1 FLUORINATED PHTHALOCYANINE COMPOUND, COLORING COMPOSITION, AND INKJET INK 富士フイルム株式会社 2023-05-25 WO disclosed
CN-115055207-A Method for preparing aryl phosphine by reducing aryl phosphine oxide 清华大学 2022-09-16 CN disclosed
US-20220149436-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2022-05-12 US disclosed
US-11283107-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2022-03-22 US disclosed
CN-113698431-A Synthesis method of phosphine (III) compound 海南大学 2021-11-26 CN disclosed
US-20010029000-A1 Photothermographic material FUJIFILM CORPORATION (JP) 2001-10-11 US disclosed
US-20010021493-A1 Comprising, on one surface of a support, a photosensitive silver halide, a silver salt of an organic acid, a reducing agent for silver ions, a binder and two or more kinds of organic polyhalogenated compounds FUJIFILM CORPORATION (JP) 2001-09-13 US disclosed
US-20010018170-A1 Method for producing grains of aliphatic acid silver salt and thermally processed image recording material FUJIFILM CORPORATION (JP) 2001-08-30 US disclosed
US-6274745-B1 CATALYST TOSOH CORPORATION (JP) 2001-08-14 US disclosed
US-6201123-B1 FOR ASYMMETRIC EPOXIDATION OF ENONES; GIVES EPOXIDES HAVING AN ENHANCED OPTICAL PURITY TECHNO POLYMER CO., LTD. (JP) 2001-03-13 US disclosed
EP-1038877-A1 Binaphthol monophosphoric acid derivative and its use Tosoh Corporation (JP) 2000-09-27 EP disclosed
US-6011181-A REDUCING THE LEVEL OF TRI-SUBSTITUTED PHOSPHINE, ARSINE AND/OR STIBINE OXIDE FROM A MIXTURE COMPRISING THE ADDITION OF A METAL SALT TO THE MIXTURE TO FORM A COMPLEX WITH THE OXIDE, AND REMOVING THE COMPLEX BASF AKTIENGESELLSCHAFT (DE) 2000-01-04 US disclosed
EP-0850902-A1 Process for reducing the level of trisubstituted phosphine, arsine and/or stibine oxide in a mixture BASF AKTIENGESELLSCHAFT (DE) 1998-07-01 EP disclosed
US-5414137-A Oxidation catalyst IDEMITSU KOSAN COMPANY LIMITED (JP) 1995-05-09 US disclosed
EP-0572036-A2 Process for preparing carbonyl compounds IDEMITSU KOSAN COMPANY LIMITED (JP) 1993-12-01 EP disclosed