SCHEMBL6402176

SCHEMBL6402176

Cc1ccc(S(=O)(=O)NC(=N)NCCC[C@@H](CO)N(C(=O)O)C(C)(C)C)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.43
LMNA P02545 3/20 0.43
ALB P02768 1/20 0.43
CYP2C9 P11712 1/20 0.43
TSHR P16473 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
ITGB3 P05106 2/20 0.40
ITGA2B P08514 2/20 0.40
NPSR1 Q6W5P4 2/20 0.38
GAA P10253 1/20 0.38
HTT P42858 1/20 0.38
OPRM1 P35372 1/20 0.36
OPRK1 P41145 1/20 0.36
PTGES O14684 1/20 0.36
CA1 P00915 2/20 0.35
CA2 P00918 2/20 0.35
CA12 O43570 1/20 0.35
CA9 Q16790 1/20 0.35
KDM4E B2RXH2 1/20 0.35
HPGD P15428 1/20 0.35

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
SCHEMBL4095386 0.79 ALDH1A1 (0.48) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL4433373 0.79 ALDH1A1 (0.50) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL27513081 0.79 ALDH1A1 (0.50) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL29438757 0.79 ALDH1A1 (0.50) ALDH1A1LMNAALBCYP2C9TSHR
Hydrochloric Acid SCHEMBL4425988 0.78 ALDH1A1 (0.49) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL14090903 0.75 ALDH1A1 (0.48) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL759821 0.75 ALDH1A1 (0.48) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL27538377 0.73 ALDH1A1 (0.54) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL29401529 0.73 ALDH1A1 (0.64) ALDH1A1LMNAALBCYP2C9TSHR
SCHEMBL10063499 0.73 ALDH1A1 (0.42) ALDH1A1LMNAALBCYP2C9TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050136017-A1 Cosmetic containing an imine reactive with the cystines of keratin fibers via a beta-elimination reaction to produce dehydroalanine and lead to formation of lanthionine in a medium free of polyhydroxylated alkane; guanidine and/or amidine imines such as dimethylguanidine; noncaustic for use on hair, skin L'OREAL S.A. (FR) 2005-06-23 US disclosed
US-20050129645-A1 Hair shaping composition comprising at least one non-hydroxide imine L'OREAL 2005-06-16 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-20050129645-A1 Hair shaping composition comprising at least one non-hydroxide imine KRT18, INHA, H1-5 ALDH1A1 1073/4885LMNA 85/4885ALB 4602/4885
US-20050136017-A1 Cosmetic containing an imine reactive with the cystines of keratin fibers via a beta-elimination reaction to produce dehydroalanine and lead to formation of lanthionine in a medium free of polyhydroxylated alkane; guanidine and/or amidine imines such as dimethylguanidine; noncaustic for use on hair, skin BHMT, KRT18, INMT ALDH1A1 1610/4885LMNA 129/4885ALB 3709/4885

“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.