Cystamine

Cystamine

SCHEMBL1133055

NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCC(=O)O.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN.NCCSSCCN

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3PDE3APDE3BPDE4APDE4BPDE4CPDE4D

The experimentally established mechanism targets of Cystamine. 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
TSHR P16473 4/20 0.59
GLRA1 P23415 1/20 0.59
SLC6A9 P48067 1/20 0.59
OR51E2 Q9H255 1/20 0.59
THPO P40225 1/20 0.59
MAPT P10636 3/20 0.56
TDP1 Q9NUW8 3/20 0.56
EHMT2 Q96KQ7 1/20 0.56
LMNA P02545 3/20 0.39
KMT2A Q03164 3/20 0.39
GABRR1 P24046 3/20 0.39
CYP1A2 P05177 3/20 0.39
THRB P10828 2/20 0.39
BLM P54132 2/20 0.39
NPSR1 Q6W5P4 2/20 0.39
HDAC2 Q92769 2/20 0.39
GABRR3 A8MPY1 1/20 0.39
GABRP O00591 1/20 0.39
GABRD O14764 1/20 0.39
HDAC3 O15379 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
Cystamine SCHEMBL8660518 1.00 TSHR (0.59) TSHRGLRA1SLC6A9OR51E2THPO
Cystamine SCHEMBL9417963 0.88 TSHR (0.67) TSHRGLRA1SLC6A9OR51E2THPO
Cystamine SCHEMBL28779847 0.86 TSHR (0.63) TSHRGLRA1SLC6A9OR51E2THPO
SCHEMBL142602 0.86 TSHR (0.72) TSHRGLRA1SLC6A9OR51E2THPO
Cystamine SCHEMBL31646100 0.85 TSHR (0.62) TSHRGLRA1SLC6A9OR51E2THPO
Cystamine SCHEMBL445194 0.85 TSHR (0.62) TSHRGLRA1SLC6A9OR51E2THPO
Hydrochloric Acid SCHEMBL1728032 0.83 TSHR (0.68) TSHRGLRA1SLC6A9OR51E2THPO
SCHEMBL12798150 0.83
Cystamine SCHEMBL9187225 0.83 TSHR (0.46) TSHRGLRA1SLC6A9OR51E2THPO
Cystamine SCHEMBL9187228 0.82 TSHR (0.59) TSHRGLRA1SLC6A9OR51E2THPO

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-20110212466-A1 Thiol-Modified Surface Immobilization Article And Method CORNING INCORPORATED 2011-09-01 US disclosed
EP-2287610-A1 Thiol-modified surface immobilization article and method Corning Incorporated (US) 2011-02-23 EP disclosed