Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | RAB9A | P51151 | 9/20 | 0.65 |
| ▸ | NPC1 | O15118 | 8/20 | 0.65 |
| ▸ | SMN1; SMN2 | Q16637 | 7/20 | 0.65 |
| ▸ | RECQL | P46063 | 1/20 | 0.65 |
| ▸ | FAAH | O00519 | 6/20 | 0.62 |
| ▸ | HPGD | P15428 | 4/20 | 0.61 |
| ▸ | LMNA | P02545 | 3/20 | 0.61 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.60 |
| ▸ | CASP1 | P29466 | 1/20 | 0.60 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.60 |
| ▸ | MAPT | P10636 | 1/20 | 0.60 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.60 |
| ▸ | MCL1 | Q07820 | 1/20 | 0.60 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.60 |
| ▸ | EPHX2 | P34913 | 1/20 | 0.59 |
| ▸ | TSHR | P16473 | 2/20 | 0.58 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.57 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.57 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.57 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL7995030 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL6767997 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL1834100 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL1837292 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL8076542 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL8600460 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL10599124 | 1.00 | RAB9A (0.65) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL8600999 | 0.98 | RAB9A (0.67) | RAB9ANPC1SMN1; SMN2RECQLFAAH | |
| SCHEMBL3765824 | 0.93 | RAB9A (0.69) | RAB9ANPC1SMN1; SMN2RECQLHPGD | |
| SCHEMBL12411578 | 0.92 | RAB9A (0.69) | RAB9ANPC1SMN1; SMN2FAAHHPGD |
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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113024418-B | Method for synthesizing alicyclic carbamate by using isopropanol as hydrogen source | 河北工业大学 | 2023-01-24 | — | — | CN | claimed |
| CN-112898184-A | Method for continuously synthesizing alicyclic carbamate | 河北工业大学 | 2021-06-04 | — | — | CN | claimed |
| JP-4320879-A | — | — | None | — | — | JP | disclosed |
| US-20240425448-A1 | METHOD FOR PRODUCING ISOCYANATE COMPOUND, METHOD FOR PRODUCING CARBAMATE COMPOUND, METHOD FOR RECOVERING AMINE COMPOUND, AND ISOCYANATE COMPOSITION | ASAHI KASEI KABUSHIKI KAISHA (JP) | 2024-12-26 | — | — | US | disclosed |
| EP-4431490-A1 | METHOD FOR PRODUCING ISOCYANATE COMPOUNDS, METHOD FOR PRODUCING CARBAMATE COMPOUNDS, METHOD FOR RECOVERING AMINE COMPOUNDS, AND ISOCYANATE COMPOSITION | Asahi Kasei Kabushiki Kaisha (JP) | 2024-09-18 | — | — | EP | disclosed |
| CN-118215651-A | Method for producing isocyanate compound, method for producing urethane compound, method for recovering amine compound, and isocyanate composition | 旭化成株式会社 | 2024-06-18 | — | — | CN | disclosed |
| WO-2023080257-A1 | METHOD FOR PRODUCING ISOCYANATE COMPOUNDS, METHOD FOR PRODUCING CARBAMATE COMPOUNDS, METHOD FOR RECOVERING AMINE COMPOUNDS, AND ISOCYANATE COMPOSITION | 旭化成株式会社 | 2023-05-11 | — | — | WO | disclosed |
| CN-112020493-B | Method for producing urethane and method for producing isocyanate | 旭化成株式会社 | 2023-04-21 | — | — | CN | disclosed |
| CN-113024418-B | Method for synthesizing alicyclic carbamate by using isopropanol as hydrogen source | 河北工业大学 | 2023-01-24 | — | — | CN | disclosed |
| EP-3838892-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2022-10-12 | — | — | EP | disclosed |
| CN-113024418-A | Method for synthesizing alicyclic carbamate by using isopropanol as hydrogen source | 河北工业大学 | 2021-06-25 | — | — | CN | disclosed |
| CN-103588680-A | Composition for transfer and storage of N-substituted carbamic acid ester and isocyanate production method | ASAHI KASEI CHEMICALS CORP | 2014-02-19 | — | — | CN | disclosed |
| CN-103553972-A | Method for the preparation of n-substituted carbamic acid ester and method for the preparation of isocyanate using the n-substituted carbamic acid ester | ASAHI KASEI CHEMICALS CORP | 2014-02-05 | — | — | CN | disclosed |
| CN-103097348-A | Process for producing carbonyl compounds | ASAHI KASEI CHEMICALS CORP (JP) | 2013-05-08 | — | — | CN | disclosed |
| CN-102471244-A | Process for producing N-substituted carbamate, process for producing isocyanate using the N-substituted carbamate, and composition for transporting and storing N-substituted carbamate containing N-substituted carbamate and aromatic hydroxy compound | ASAHI KASEI CHEMICALS CORP (JP) | 2012-05-23 | — | — | CN | disclosed |
| US-6399292-B2 | A MATTING AGENT HAVING A SOFTENING TEMPERATURE OF FROM 100 TO 500 DEGREES C. IS CONTAINED AT LEAST ON ONE SIDE OF THE SUPPORT. | FUJI PHOTO FILM CO., LTD. (JP) | 2002-06-04 | — | — | US | disclosed |
| US-20020015924-A1 | PHOTOTHERMOGRAPHIC PHOTOSENSITIVE MATERIAL AND PHOTOTHEMOGRAPHIIC METHOD | FUJIFILM CORPORATION (JP) | 2002-02-07 | — | — | US | disclosed |
| US-6300053-B1 | SUPPORT WITH SURFACE LAYER, PHOTOSENSITIVITY AND NONPHOTOSENSITIVE LAYER, SUPPORTS AND BLEACHABLE CYANINE DYE WITH SILVER HALIDE LAYER | FUJI PHOTO FILM CO., LTD. (JP) | 2001-10-09 | — | — | US | disclosed |
| US-6165706-A | MULTILAYER ELEMENT PHOTOTHERMOGRAPHIC ELEMENT | FUJI PHOTO FILM CO., LTD. (JP) | 2000-12-26 | — | — | US | disclosed |
| JP-H04320879-A | DEVELOPING INK | FUJI PHOTO FILM CO LTD | 1992-11-11 | — | — | JP | 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 (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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20240425448-A1 | METHOD FOR PRODUCING ISOCYANATE COMPOUND, METHOD FOR PRODUCING CARBAMATE COMPOUND, METHOD FOR RECOVERING AMINE COMPOUND, AND ISOCYANATE COMPOSITION | IDH3A, CA7, C9 | RAB9A 3205/4885NPC1 666/4885SMN1; SMN2 2354/4885 |
“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.