Indinavir Anhydrous

Indinavir Anhydrous

SCHEMBL17787450

CC(C)(C)NC(=O)C1CN(Cc2cccnc2)CCN1C[C@@H](O)C[C@@H](Cc1ccccc1)C(=O)NC1c2ccccc2C[C@H]1O

nearest known ligand 0.99

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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The experimentally established mechanism targets of Indinavir Anhydrous. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 18/20 0.99
ABCC3 O15438 1/20 0.99
ABCB11 O95342 1/20 0.99
ABCB1 P08183 1/20 0.99
TACR2 P21452 1/20 0.99
TBXAS1 P24557 1/20 0.99
SLC47A2 Q86VL8 1/20 0.99
SLC47A1 Q96FL8 1/20 0.99
NR1I2 O75469 1/20 0.95
LMNA P02545 1/20 0.95
CYP2D6 P10635 13/20 0.75
CYP2C9 P11712 6/20 0.55

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
Indinavir Anhydrous SCHEMBL1176257 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL7752012 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL19760130 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL13039789 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL20099152 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL6908581 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL19460567 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL21683359 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL21578565 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL13575769 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2

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-9956260-B1 Treatment of HIV-1 infection and AIDS THE J. DAVID GLADSTONE INSTITUTES (US) 2018-05-01 US disclosed
US-9352010-B2 Treatment of HIV-1 infection and AIDS THE J. DAVID GLADSTONE INSTITUTES (US) 2016-05-31 US disclosed