Hymecromone

Hymecromone

SCHEMBL3272842

Cc1cc(=O)oc2cc(O)ccc12.O=P(O)(O)O

nearest known ligand 0.87

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Hymecromone. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDR known ✓ P35968 1/20 0.87
▸ HSD17B3 P37058 8/20 0.87
▸ ALDH1A1 P00352 7/20 0.87
▸ KDM4E B2RXH2 6/20 0.87
▸ CA12 O43570 6/20 0.87
▸ CA9 Q16790 6/20 0.87
▸ HPGD P15428 4/20 0.87
▸ HSD17B10 Q99714 4/20 0.87
▸ GAA P10253 4/20 0.87
▸ GLA P06280 3/20 0.87
▸ AKR1B1 P15121 3/20 0.87
▸ MAOB P27338 3/20 0.87
▸ CASP1 P29466 2/20 0.87
▸ CASP7 P55210 2/20 0.87
▸ MCL1 Q07820 2/20 0.87
▸ LMNA P02545 1/20 0.87
▸ CYP1A2 P05177 1/20 0.87
▸ CYP2C9 P11712 1/20 0.87
▸ UGT1A1 P22309 1/20 0.87
▸ DYRK1A Q13627 1/20 0.61

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
Hymecromone SCHEMBL29364837 0.93 HSD17B3 (1.00) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL24150 0.93 HSD17B3 (1.00) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL2357040 0.93 HSD17B3 (1.00) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL29624431 0.93 HSD17B3 (1.00) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL31014 0.92 HSD17B3 (0.96) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL27924142 0.92 HSD17B3 (0.96) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL27728511 0.90 HSD17B3 (0.93) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL2256610 0.89 ALDH1A1 (0.90) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL7594956 0.87 KDM4E (0.87) HSD17B3ALDH1A1KDM4ECA12CA9
Hymecromone SCHEMBL28882003 0.87 KDM4E (0.87) HSD17B3ALDH1A1KDM4ECA12CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119224316-B Detection method and application for botulinum neurotoxin type B 兰州生物技术开发有限公司 2025-05-16 — — CN claimed
CN-119708627-A Preparation method of nano calcium carbonate with good high temperature resistance and flame retardance dispersibility 湖北三峡实验室 2025-03-28 — — CN claimed
CN-119438162-A Ce-based3+/Ce4+Fluorescence and colorimetric dual-mode detection method for simultaneously measuring hydrogen peroxide and organic phosphorus by cascade simulated enzyme reaction 临沂大学 2025-02-14 — — CN claimed
CN-119224316-A Detection method and application for botulinum neurotoxin type B 兰州生物技术开发有限公司 2024-12-31 — — CN claimed
CN-118773000-A Alkaline phosphatase detection device and method for adipose-derived stem cell osteogenic differentiation 江苏圣澄干细胞科技有限公司 2024-10-15 — — CN claimed
CN-116410310-B anti-CMLC-1 monoclonal antibody 8A3 and application thereof 北京普恩光德生物科技开发有限公司 2023-10-27 — — CN claimed
CN-116410310-A anti-CMLC-1 monoclonal antibody 8A3 and application thereof 北京普恩光德生物科技开发有限公司 2023-07-11 — — CN claimed
CN-115478094-A Enzyme substrate method determination agent for total number of bacterial colonies in water and preparation method thereof 奎泰斯特(上海)科技有限公司 2022-12-16 — — CN claimed
CN-111229193-B Application of zirconium dioxide nano particles as alkaline phosphatase nano mimics 重庆师范大学 2022-10-18 — — CN claimed
CN-112710644-B Zymogram method for determining two-dimensional spatial distribution of activity of rhizosphere phosphatase of aquatic plants 中国科学院南京地理与湖泊研究所 2022-04-19 — — CN claimed
WO-2010039899-A2 METHOD FOR MONITORING INTRACELLULAR TYROSINE PHOSPHATASE ACTIVITY UNIVERSITY OF SOUTHERN CALIFORNIA (US) 2010-04-08 — — WO claimed
US-20100086957-A1 METHOD FOR MONITORING INTRACELLULAR TYROSINE PHOSPHATASE ACTIVITY UNIVERSITY OF SOUTHERN CALIFORNIA (US) 2010-04-08 — — US claimed
CN-101551333-A Composition for cell permeabilization comprising NOG, HMP, rubidium chloride and/or lithium chloride for detecting living cells on a membrane MILLIPORE CORP (US) 2009-10-07 — — CN claimed
EP-0724015-B1 Novel alkaline phosphatase, its production and use TOYO BOSEKI (JP) 2004-03-31 — — EP claimed
EP-0816514-B1 Enzyme substrate TOSOH CORP (JP) 2003-04-09 — — EP claimed
US-5895819-A Enzyme substrate TOSOH CORPORATION (JP) 1999-04-20 — — US claimed
US-5821061-A REACTING A LIGAND IN A SAMPLE WITH A SUBSTANCE BONDED WITH A BACILLUS ALKALINE PHOSPHATASE TOYO BOSEKI KABUSHIKI KAISHA (JP) 1998-10-13 — — US claimed
EP-0816514-A2 Enzyme substrate Tosoh Corporation (JP) 1998-01-07 — — EP claimed
EP-0724015-A2 Novel alkaline phosphatase, its production and use TOYO BOSEKI KABUSHIKI KAISHA (JP) 1996-07-31 — — EP claimed
US-5055390-A Amphiphilic compound migrating into droplet, interacting with biological entity; measuring fluorescence MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1991-10-08 — — US claimed

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

For each of this compound's patents that has machine-readable text (1 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-20100086957-A1 METHOD FOR MONITORING INTRACELLULAR TYROSINE PHOSPHATASE ACTIVITY PTPRCAP, PTPRC, PTPA KDR 2569/4885HSD17B3 4181/4885ALDH1A1 3727/4885

“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.

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