SCHEMBL13301479

SCHEMBL13301479

CCN(CC)c1ccc(C(=O)c2ccccc2C(=O)OCC(C)(C)COC(=O)c2ccccc2C(=O)c2ccc(N(CC)CC)cc2O)c(O)c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SMN1; SMN2 Q16637 5/20 0.66
▸ L3MBTL1 Q9Y468 3/20 0.66
▸ MEN1 O00255 2/20 0.66
▸ KMT2A Q03164 2/20 0.66
▸ ALDH1A1 P00352 5/20 0.52
▸ KDM4E B2RXH2 4/20 0.52
▸ GAA P10253 3/20 0.52
▸ POLB P06746 1/20 0.52
▸ SERPINE1 P05121 1/20 0.40
▸ TSHR P16473 2/20 0.39
▸ CDC25B P30305 1/20 0.39
▸ MAPT P10636 5/20 0.39
▸ MAPK1 P28482 1/20 0.39
▸ HTT P42858 1/20 0.39
▸ LMNA P02545 3/20 0.39
▸ HPGD P15428 2/20 0.39
▸ CYP1A2 P05177 1/20 0.39
▸ PGR P06401 1/20 0.39
▸ CYP3A4 P08684 1/20 0.39
▸ ADORA3 P0DMS8 1/20 0.39

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
SCHEMBL13301484 0.95 SMN1; SMN2 (0.63) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL14069299 0.94 SMN1; SMN2 (0.62) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL13301482 0.94 SMN1; SMN2 (0.58) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL13301483 0.92 SMN1; SMN2 (0.67) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL13301470 0.91 SMN1; SMN2 (0.66) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL12431397 0.88 SMN1; SMN2 (0.72) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL13301476 0.88 L3MBTL1 (0.72) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL14529371 0.86 MEN1 (0.53) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL13301485 0.86 L3MBTL1 (0.69) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1
SCHEMBL12792825 0.86 SMN1; SMN2 (0.69) SMN1; SMN2L3MBTL1MEN1KMT2AALDH1A1

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9656103-B2 Light protecting-effective cosmetic or dermatological preparations BASF SE (DE) 2017-05-23 — — US disclosed
US-9656103-B2 Light protecting-effective cosmetic or dermatological preparations BASF SE (DE) 2017-05-23 — — US disclosed
EP-1606270-B1 Symmetrical triazine derivatives BASF SE (DE) 2013-08-14 — — EP disclosed
US-20100143274-A1 USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS CIBA CORPORATION (US) 2010-06-10 — — US disclosed
US-20100143274-A1 USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS CIBA CORPORATION (US) 2010-06-10 — — US disclosed
EP-1768644-B1 LIGHT PROTECTING-EFFECTIVE COSMETIC OR DERMATOLOGICAL PREPARATIONS CIBA HOLDING INC (CH) 2009-02-18 — — EP disclosed
WO-2008107347-A2 USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS BASF SE (CH) 2008-09-12 — — WO disclosed
US-7374749-B2 Amino substituted hydroxyphenyl benzophenone derivatives CIBA SPECIALTY CHEMICALS CORP. (US) 2008-05-20 — — US disclosed
US-7374749-B2 Amino substituted hydroxyphenyl benzophenone derivatives CIBA SPECIALTY CHEMICALS CORP. (US) 2008-05-20 — — US disclosed
US-20080075746-A1 Dispersing insoluble or sparingly soluble micronized substance in oil or water phase; adding soluble ultraviolet radiation filter that is not a cosmetic UV absorber; remarkable increase in (SPF) sun protection factor; sunscreen agents CIBA SPECIALTY CHEMICALS CORPORATION 2008-03-27 — — US disclosed
US-20080075746-A1 Dispersing insoluble or sparingly soluble micronized substance in oil or water phase; adding soluble ultraviolet radiation filter that is not a cosmetic UV absorber; remarkable increase in (SPF) sun protection factor; sunscreen agents CIBA SPECIALTY CHEMICALS CORPORATION 2008-03-27 — — US disclosed
US-7311897-B2 Triazines which are symmetrically substituted by phenyl, biphenyl, triphenyl or naphthyl can be used as highly effective UV absorbers for cosmetic applications CIBA SPECIALTY CHEMICALS CORPORATION (US) 2007-12-25 — — US disclosed
US-7311897-B2 Triazines which are symmetrically substituted by phenyl, biphenyl, triphenyl or naphthyl can be used as highly effective UV absorbers for cosmetic applications CIBA SPECIALTY CHEMICALS CORPORATION (US) 2007-12-25 — — 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 (2 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-20100143274-A1 USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS MAOA, MAOB, ACMSD SMN1; SMN2 2903/4885L3MBTL1 4501/4885MEN1 237/4885
US-20080075746-A1 Dispersing insoluble or sparingly soluble micronized substance in oil or water phase; adding soluble ultraviolet radiation filter that is not a cosmetic UV absorber; remarkable increase in (SPF) sun protection factor; sunscreen agents CUTA, MITF, MIF SMN1; SMN2 2442/4885L3MBTL1 4863/4885MEN1 1235/4885

“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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