SCHEMBL341137

SCHEMBL341137

COc1cc(C(=O)Cl)ccc1OCc1ccccc1

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 2/20 0.73
RAB9A P51151 2/20 0.73
SMN1; SMN2 Q16637 2/20 0.73
HPGD P15428 1/20 0.73
MRGPRX4 Q96LA9 2/20 0.65
SMPD1 P17405 2/20 0.64
HDAC1 Q13547 1/20 0.64
HDAC8 Q9BY41 1/20 0.64
HDAC6 Q9UBN7 1/20 0.64
KDM4E B2RXH2 1/20 0.62
MEN1 O00255 1/20 0.62
KMT2A Q03164 1/20 0.62
RXRA P19793 1/20 0.61
ATM Q13315 1/20 0.59
ABCB1 P08183 1/20 0.57
CYP1A2 P05177 1/20 0.55
CYP3A4 P08684 1/20 0.55
MAPT P10636 1/20 0.55
CYP2C9 P11712 1/20 0.55
CYP2C19 P33261 1/20 0.55

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
SCHEMBL184987 0.94 SMPD1 (0.71) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL29557477 0.91 HPGD (0.59) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL1599431 0.91 HPGD (0.59) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL20463492 0.89 MRGPRX4 (0.65) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL242563 0.88 MRGPRX4 (0.77) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL27881765 0.88 NPC1 (0.77) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL3944668 0.87 MRGPRX4 (0.59) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL31025721 0.87 NPC1 (0.75) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL340620 0.87 NPC1 (0.75) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4
SCHEMBL11277266 0.87 MRGPRX4 (0.75) NPC1RAB9ASMN1; SMN2HPGDMRGPRX4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3580389-B1 NOVEL METHODS FOR PROCESSING LIGNOCELLULOSIC MATERIAL CMBLU ENERGY AG (DE) 2025-09-17 EP disclosed
EP-3580302-B1 REDOX FLOW BATTERY ELECTROLYTES CMBLU ENERGY AG (DE) 2025-09-17 EP disclosed
US-20250192176-A1 Redox Flow Battery Electrolytes CMBLU ENERGY AG (DE) 2025-06-12 US disclosed
US-20240356030-A1 Redox Flow Battery Electrolytes CMBLU ENERGY AG (DE) 2024-10-24 US disclosed
US-20240318382-A1 Sulfonated Lignin-Derived Compounds And Uses Thereof CMBLU ENERGY AG (DE) 2024-09-26 US disclosed
US-11891349-B2 Aminated lignin-derived compounds and uses thereof CMBLU ENERGY AG (DE) 2024-02-06 US disclosed
US-11831017-B2 Redox flow battery electrolytes CMBLU ENERGY AG (DE) 2023-11-28 US disclosed
US-11831017-B2 Redox flow battery electrolytes CMBLU ENERGY AG (DE) 2023-11-28 US disclosed
US-11831017-B2 Redox flow battery electrolytes CMBLU ENERGY AG (DE) 2023-11-28 US disclosed
US-11788228-B2 Methods for processing lignocellulosic material CMBLU ENERGY AG (DE) 2023-10-17 US disclosed
EP-0635480-B1 Anthracene derivatives WAKO PURE CHEM IND LTD (JP) 1997-03-19 EP disclosed
CN-1137895-A Prevention and curing agent for c attenuation living vaccine EISAI CO LTD (JP) 1996-12-18 CN disclosed
US-5576359-A ANTHRACENE DERIVATIVE, SOLVENT, COMPOUND CONTAINING GLYCIDYL GROUPS WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 1996-11-19 US disclosed
EP-0636941-B1 Deep ultraviolet absorbent and its use in pattern formation WAKO PURE CHEM IND LTD (JP) 1996-03-20 EP disclosed
US-5498748-A PHENOLIC CROSSLINKER FOR A POLYGLYCIDYL METHACRYLATE TO FORM A MATERIAL USED AS AN ANTIREFLECTION COATING FOR DEEP UV LIGHT SUCH AS KRF EXIMER LASERS IN SEMICONDUCTOR PHOTORESISTS WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 1996-03-12 US disclosed
EP-0636941-A1 Deep ultraviolet absorbent and its use in pattern formation WAKO PURE CHEMICAL INDUSTRIES LTD (JP) 1995-02-01 EP disclosed
EP-0635480-A1 Anthracene derivatives WAKO PURE CHEMICAL INDUSTRIES LTD (JP) 1995-01-25 EP disclosed
EP-0613879-A1 PHELLODENDRINE ANALOGS AND ALLERGY TYPE IV SUPPRESSOR CONTAINING THE SAME AS ACTIVE INGREDIENT TSUMURA & CO. (JP) 1994-09-07 EP disclosed
US-4618680-A ANTIARRHYTHMIA AGENTS MEAD JOHNSON & COMPANY (US) 1986-10-21 US disclosed
US-4332803-A ANTIARRHYTHMIA AGENTS MEAD JOHNSON & COMPANY (US) 1982-06-01 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (6 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20240356030-A1 Redox Flow Battery Electrolytes GPX4, GPX1, MPO NPC1 3816/4885RAB9A 747/4885SMN1; SMN2 3204/4885
US-11788228-B2 Methods for processing lignocellulosic material DCXR, LCT, AGL NPC1 2208/4885RAB9A 4443/4885SMN1; SMN2 4294/4885
US-11891349-B2 Aminated lignin-derived compounds and uses thereof NQO1, DCXR, NOX4 NPC1 4192/4885RAB9A 2645/4885SMN1; SMN2 4488/4885
US-11831017-B2 Redox flow battery electrolytes GPX1, GPX4, NOX4 NPC1 3240/4885RAB9A 1347/4885SMN1; SMN2 4095/4885
US-20250192176-A1 Redox Flow Battery Electrolytes GPX1, GPX4, CYBB NPC1 3781/4885RAB9A 570/4885SMN1; SMN2 3297/4885
US-20240318382-A1 Sulfonated Lignin-Derived Compounds And Uses Thereof SQOR, NQO1, NOX4 NPC1 4337/4885RAB9A 3114/4885SMN1; SMN2 3589/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.