SCHEMBL1031865

SCHEMBL1031865

O=[PH](OCC1CO1)OCC1CO1

nearest known ligand 0.42

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 5/20 0.42
ALDH1A1 P00352 9/20 0.41
MAPK1 P28482 1/20 0.38
TP53 P04637 5/20 0.38
CYP3A4 P08684 2/20 0.38
SMN1; SMN2 Q16637 3/20 0.37
TDP1 Q9NUW8 3/20 0.35
HIF1A Q16665 2/20 0.34
PKM P14618 2/20 0.34
LMNA P02545 1/20 0.34
GAA P10253 1/20 0.34
GLA P06280 1/20 0.32
HBB P68871 1/20 0.32
MAPT P10636 2/20 0.31
HPGD P15428 2/20 0.31
MEN1 O00255 1/20 0.31
CYP1A2 P05177 1/20 0.31
KMT2A Q03164 1/20 0.31
PPARG P37231 1/20 0.31

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
Propane SCHEMBL9456514 0.93 SMN1; SMN2 (0.42) TSHRALDH1A1MAPK1TP53CYP3A4
SCHEMBL16232411 0.87 TSHR (0.48) TSHRALDH1A1MAPK1TP53CYP3A4
Biphenyl SCHEMBL1979668 0.82 TDP1 (0.50) TSHRALDH1A1TP53CYP3A4SMN1; SMN2
SCHEMBL7242511 0.81 ALDH1A1 (0.42) TSHRALDH1A1MAPK1TP53CYP3A4
SCHEMBL8677271 0.80
Hydantoin SCHEMBL11558895 0.77
SCHEMBL11664866 0.77 TSHR (0.63) TSHRALDH1A1MAPK1TP53CYP3A4
Butane SCHEMBL10485249 0.73 SMN1; SMN2 (0.42) TSHRALDH1A1MAPK1TP53CYP3A4
SCHEMBL7934138 0.73 SMN1; SMN2 (0.42) TSHRALDH1A1MAPK1TP53CYP3A4
Phosphonic Acid SCHEMBL974904 0.72 TSHR (0.52) TSHRALDH1A1MAPK1TP53CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118146260-A Unsaturated cationic phosphonate modified bis-salicylaldehyde primary diamine and preparation method thereof 长治学院 2024-06-07 CN claimed
CN-118065133-A Unsaturated ion phosphonate composition and preparation method thereof 江苏海洋大学 2024-05-24 CN claimed
CN-118063505-A Unsaturated gemini Ji An acid ester and preparation method thereof 江苏海洋大学 2024-05-24 CN claimed
JP-3447290-B2 2003-09-16 JP claimed
EP-0543303-B1 Hydrophilic hydrogels having a high swelling capacity HOECHST AG (DE) 1997-02-12 EP claimed
EP-0412425-B1 Flame retardant casting resins as moulding compounds SIEMENS AG (DE) 1996-11-13 EP claimed
EP-0667877-A1 UNITARY REACTION RESIN SYSTEMS SIEMENS AKTIENGESELLSCHAFT (DE) 1995-08-23 EP claimed
WO-1994010223-A1 UNITARY REACTION RESIN SYSTEMS SIEMENS AKTIENGESELLSCHAFT (DE) 1994-05-11 WO claimed
US-4654277-A CHEMICALLY BONDING, CONSTRUCTION MATERIALS THE DOW CHEMICAL COMPANY (US) 1987-03-31 US claimed
JP-5230382-A None JP disclosed
EP-4479013-B1 PERSONAL CARE POD DOW SILICONES CORP (US) 2026-01-21 EP disclosed
EP-4479460-B1 FREE STANDING FILM DOW SILICONES CORP (US) 2026-01-21 EP disclosed
US-12516269-B2 Detergent formulation DOW SILICONES CORPORATION (US) 2026-01-06 US disclosed
US-12454663-B2 Cleaning bar DOW GLOBAL TECHNOLOGIES LLC (US) 2025-10-28 US disclosed
EP-0412425-A1 Flame retardant casting resins as moulding compounds SIEMENS AKTIENGESELLSCHAFT (DE) 1991-02-13 EP disclosed
US-4692355-A LEWIS ACIDS OR BASES THE DOW CHEMICAL COMPANY (US) 1987-09-08 US disclosed
EP-0220072-A2 Method of improving flame resistance of epoxy resins and resulting compositions THE DOW CHEMICAL COMPANY (US) 1987-04-29 EP disclosed
WO-1987002372-A1 OXIRANE GROUP CONTAINING PHOSPHONATES IN FLAME RESISTANT EPOXY RESINS. THE DOW CHEMICAL COMPANY (US) 1987-04-23 WO disclosed
US-4654277-A CHEMICALLY BONDING, CONSTRUCTION MATERIALS THE DOW CHEMICAL COMPANY (US) 1987-03-31 US disclosed
US-4632973-A OXIRANYL-ALKYLPHOSPHONATE THE DOW CHEMICAL COMPANY (US) 1986-12-30 US disclosed