Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CALM1 | P0DP23 | 1/20 | 0.57 |
| ▸ | LTA4H | P09960 | 2/20 | 0.50 |
| ▸ | HTR2A | P28223 | 1/20 | 0.48 |
| ▸ | LMNA | P02545 | 1/20 | 0.47 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.46 |
| ▸ | BCL2 | P10415 | 1/20 | 0.46 |
| ▸ | BCL2L1 | Q07817 | 1/20 | 0.46 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.46 |
| ▸ | CYP2D6 | P10635 | 2/20 | 0.46 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.46 |
| ▸ | MEN1 | O00255 | 1/20 | 0.46 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.46 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.46 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.46 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.46 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.46 |
| ▸ | TSHR | P16473 | 1/20 | 0.45 |
| ▸ | IDH1 | O75874 | 1/20 | 0.43 |
| ▸ | KEAP1 | Q14145 | 1/20 | 0.43 |
| ▸ | FFAR1 | O14842 | 2/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL9741301 | 0.95 | CALM1 (0.55) | CALM1LTA4HHTR2ATAAR1BCL2 | |
| SCHEMBL275838 | 0.95 | CALM1 (0.55) | CALM1LTA4HHTR2ATAAR1BCL2 | |
| SCHEMBL29940610 | 0.95 | CALM1 (0.55) | CALM1LTA4HHTR2ATAAR1BCL2 | |
| SCHEMBL27614158 | 0.93 | CALM1 (0.52) | CALM1LTA4HHTR2ATAAR1BCL2 | |
| Hydrochloric Acid SCHEMBL21175607 | 0.93 | CALM1 (0.52) | CALM1LTA4HHTR2ALMNATAAR1 | |
| SCHEMBL10863097 | 0.93 | CALM1 (0.52) | CALM1LTA4HHTR2ALMNATAAR1 | |
| SCHEMBL8095627 | 0.93 | LTA4H (0.53) | CALM1LTA4HHTR2ATAAR1TSHR | |
| SCHEMBL7192027 | 0.91 | HTR2A (0.54) | CALM1LTA4HHTR2ATAAR1BCL2 | |
| SCHEMBL2140999 | 0.91 | HTR2A (0.54) | CALM1LTA4HHTR2ATAAR1BCL2 | |
| SCHEMBL8087746 | 0.87 | BCL2 (0.45) | CALM1LTA4HHTR2ALMNABCL2 |
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 67 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2029512-B1 | PROCESS FOR PREPARING ACROLEIN OR ACRYLIC ACID OR A MIXTURE THEREOF FROM PROPANE | BASF SE (DE) | 2017-10-11 | — | — | EP | disclosed |
| EP-1546073-B1 | METHOD FOR THE PRODUCTION OF AT LEAST ONE PARTIAL PROPYLENE OXIDATION AND/OR AMMOXIDATION PRODUCT | BASF SE (DE) | 2017-01-11 | — | — | EP | disclosed |
| EP-1765753-B1 | METHOD FOR THE PRODUCTION OF ACROLEIN, ACRYLIC ACID, OR A MIXTURE THEREOF BY MEANS OF HETEROGENEOUSLY CATALYZED PARTIAL GAS PHASE OXIDATION OF PROPYLENE | BASF SE (DE) | 2016-10-05 | — | — | EP | disclosed |
| EP-1765754-B1 | METHOD FOR THE PRODUCTION OF ACROLEIN, ACRYLIC ACID, OR A MIXTURE THEREOF FROM PROPANE | BASF SE (DE) | 2015-12-09 | — | — | EP | disclosed |
| EP-1881952-B1 | METHOD FOR THE PRODUCTION OF AT LEAST ONE FINAL PRODUCT BY PARTIAL OXIDATION AND/OR AMMOXIDATION OF PROPYLENE | BASF SE (DE) | 2015-08-19 | — | — | EP | disclosed |
| EP-1642879-B1 | Method for producing acrolein and/or acrylic acid or a mixture thereof from propane and/or propene | BASF SE (DE) | 2014-05-21 | — | — | EP | disclosed |
| US-8431743-B2 | Preparation of acrylic acid by heterogeneously catalyzed partial gas phase oxidation of propylene | BASF AKTIENGESELLSCHAFT (DE) | 2013-04-30 | — | — | US | disclosed |
| US-8338640-B2 | Pressurized vapor phase; dividing gases streams; circulation; discharging; forming acrylic acid, methacrylic acid | BASF AKTIENGESELLSCHAFT (DE) | 2012-12-25 | — | — | US | disclosed |
| EP-1765759-B1 | METHOD FOR THE PRODUCTION OF ACRYLIC ACID BY MEANS OF HETEROGENEOUSLY CATALYZED PARTIAL GAS PHASE OXIDATION OF PROPYLENE | BASF SE (DE) | 2011-08-17 | — | — | EP | disclosed |
| US-7897812-B2 | Propane is partially dehydrogenated in a reaction zone, hydrogen formed is incinerated partly to water and product gas is charged directly to another reaction zone, where propylene formed is partially oxidized; product removed; CO2 scrubbed from residual gas and discharged recycled to first reaction zone | BASF AKTIENGESELLSCHAFT (DE) | 2011-03-01 | — | — | US | disclosed |
| US-6350906-B2 | VAPOR PHASE CATALYTIC OXIDATION | BASF AKTIENGESELLSCHAFT (DE) | 2002-02-26 | — | — | US | disclosed |
| US-20010056204-A1 | CONTINUOUS RECOVERY OF (METH)ACRYLIC ACID | BASF AKTIENGESELLSCHAFT (DE) | 2001-12-27 | — | — | US | disclosed |
| WO-2001096271-A2 | METHOD FOR PRODUCING ACROLEIN AND/OR ACRYLIC ACID | BASF AKTIENGESELLSCHAFT (DE) | 2001-12-20 | — | — | WO | disclosed |
| US-20010007043-A1 | CONTINUOUS RECOVERY OF (METH)ACRYLIC ACID | BASF AKTIENGESELLSCHAFT (DE) | 2001-07-05 | — | — | US | disclosed |
| EP-0708077-B1 | Diamino compounds and methods for preparing them | CHISSO CORP (JP) | 2000-12-27 | — | — | EP | disclosed |
| EP-0982287-A1 | Process for the continuous recovery of (meth)acrylic acid | BASF AKTIENGESELLSCHAFT (DE) | 2000-03-01 | — | — | EP | disclosed |
| EP-0982289-A2 | Process for the continuous isolation of (meth)acrylic acid | BASF AKTIENGESELLSCHAFT (DE) | 2000-03-01 | — | — | EP | disclosed |
| US-5663440-A | Diamino compounds and methods for preparing them | CHISSO CORPORATION (JP) | 1997-09-02 | — | — | US | disclosed |
| EP-0708077-A1 | Diamino compounds and methods for preparing them | CHISSO CORPORATION (JP) | 1996-04-24 | — | — | EP | disclosed |
| US-4110370-A | Method of separating high-boiling or non-volatile materials | BASF AKTIENGESELLSCHAFT (DE) | 1978-08-29 | — | — | US | disclosed |