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Rapamycin - ≥95%(HPLC), high purity , CAS No.53123-88-9

In stock
Item Number
S293790
Grouped product items
SKUSizeAvailabilityPrice Qty
S293790-50mg
50mg
4
$19.90
S293790-250mg
250mg
4
$79.90
S293790-1g
1g
3
$169.90

Basic Description

SynonymsAY 22989 | AY-22989 | CHEBI:9168 | EC 610-965-5 | HMS2089A21 | RAPA | (1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-12-{(2S)-1-[(1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl]propan-2-yl}-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl
Specifications & PurityMoligand™, ≥95%(HPLC)
Biochemical and Physiological MechanismsA macrocyclic triene antibiotic that binds to and inhibits the molecular target of rapamycin (mTOR). It forms a complex with FKBP12 that binds to and inhibits the molecular target of rapamycin (mTOR). Rapamycin is a potent immunosuppressant and has antica
Storage TempStore at -20°C,Argon charged
Shipped InIce chest + Ice pads
GradeMoligand™
Product Description

Anti-fungal and immunosuppressant. Selectively inhibits the mammalian target of rapamycin (mTOR) and blocks the subsequent activation of p70 S6 kinase (IC50 = 50 pM). Specifically inhibits mTORC1, but mTORC2 that phosphorylates Akt at Ser473 appears to be insensitive to rapamycin. Prevents the translational activation of IGF-II. Also prevents resting T-cells from entering the cell cycle, but does not directly arrest cell cycle progression. Shown to inhibit later signaling events, such as p110Rb phosphorylation, p34cdc2 kinase activation, and cyclin A synthesis. Exhibits strong binding to FK-506 binding proteins. Also reported to induce apoptosis in a murine B-cell line, to inhibit lymphokine-induced cell proliferation at the G1 phase, and to irreversibly arrest Saccharomyces cerevisiae cells in the G1 phase.

Associated Targets(Human)

FKBP1A Tclin Peptidyl-prolyl cis-trans isomerase FKBP1A (10 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
FKBP1B Tchem Peptidyl-prolyl cis-trans isomerase FKBP1B (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
FKBP5 Tchem Peptidyl-prolyl cis-trans isomerase FKBP5 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EIF4E Tchem Eukaryotic translation initiation factor 4E (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PDCD4 Tchem Programmed cell death protein 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MTOR Tclin Serine/threonine-protein kinase mTOR (7 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid504763502
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504763502
IUPAC Name (1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl]propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
INCHI InChI=1S/C51H79NO13/c1-30-16-12-11-13-17-31(2)42(61-8)28-38-21-19-36(7)51(60,65-38)48(57)49(58)52-23-15-14-18-39(52)50(59)64-43(33(4)26-37-20-22-40(53)44(27-37)62-9)29-41(54)32(3)25-35(6)46(56)47(63-10)45(55)34(5)24-30/h11-13,16-17,25,30,32-34,36-40,42-44,46-47,53,56,60H,14-15,18-24,26-29H2,1-10H3/b13-11+,16-12+,31-17+,35-25+/t30-,32-,33-,34-,36-,37+,38+,39+,40-,42+,43+,44-,46-,47+,51-/m1/s1
InChi Key QFJCIRLUMZQUOT-HPLJOQBZSA-N
Canonical SMILES CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)O)C)C)O)OC)C)C)C)OC
Isomeric SMILES C[C@@H]1CC[C@H]2C[C@@H](/C(=C/C=C/C=C/[C@H](C[C@H](C(=O)[C@@H]([C@@H](/C(=C/[C@H](C(=O)C[C@H](OC(=O)[C@@H]3CCCCN3C(=O)C(=O)[C@@]1(O2)O)[C@H](C)C[C@@H]4CC[C@H]([C@@H](C4)OC)O)C)/C)O)OC)C)C)/C)OC
RTECS VE6250000
Molecular Weight 914.19
Reaxy-Rn 5848501

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

19 results found

Lot NumberCertificate TypeDateItem
C2505451Certificate of AnalysisMar 07, 2025 S293790
C2505452Certificate of AnalysisMar 07, 2025 S293790
C2505455Certificate of AnalysisMar 07, 2025 S293790
B2527150Certificate of AnalysisFeb 28, 2025 S293790
L2403373Certificate of AnalysisNov 22, 2024 S293790
L2403374Certificate of AnalysisNov 22, 2024 S293790
A2307041Certificate of AnalysisOct 21, 2024 S293790
A2307034Certificate of AnalysisOct 21, 2024 S293790
A2307025Certificate of AnalysisOct 21, 2024 S293790
A2307033Certificate of AnalysisOct 11, 2024 S293790
A2307038Certificate of AnalysisOct 11, 2024 S293790
E2225238Certificate of AnalysisFeb 23, 2024 S293790
E2225235Certificate of AnalysisFeb 23, 2024 S293790
E2225234Certificate of AnalysisFeb 23, 2024 S293790
A2422188Certificate of AnalysisNov 10, 2022 S293790
A2307032Certificate of AnalysisNov 10, 2022 S293790
H2312240Certificate of AnalysisNov 10, 2022 S293790
C2428063Certificate of AnalysisNov 10, 2022 S293790
A2221042Certificate of AnalysisApr 28, 2021 S293790

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Chemical and Physical Properties

SolubilitySoluble in DMSO at 50mg/ml or methanol at 25mg/mlSoluble in alcohol, dimethyl sulfoxide and dimethyl formamide. Insoluble in water.
SensitivityHeat sensitive.
Specific Rotation[α]-150° (C=0.2,MeOH)
Melt Point(°C)177 °C(dec.)
Molecular Weight914.200 g/mol
XLogP36.000
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count13
Rotatable Bond Count6
Exact Mass913.555 Da
Monoisotopic Mass913.555 Da
Topological Polar Surface Area195.000 Ų
Heavy Atom Count65
Formal Charge0
Complexity1760.000
Isotope Atom Count0
Defined Atom Stereocenter Count15
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count4
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds4
Covalently-Bonded Unit Count1

Safety and Hazards(GHS)

Pictogram(s) GHS08
Signal Danger
Hazard Statements

H351:Suspected of causing cancer

H372:Causes damage to organs through prolonged or repeated exposure

H361:Suspected of damaging fertility or the unborn child

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P260:Do not breathe dust/fume/gas/mist/vapors/spray.

P270:Do not eat, drink or smoke when using this product.

P203:Obtain, read and follow all safety instructions before use.

P318:if exposed or concerned, get medical advice.

P319:Get medical help if you feel unwell.

RTECS VE6250000
Reaxy-Rn 5848501
Merck Index 8114

Specifications

Purity(HPLC)95-100(%)
Nitrogen by Elemental Analysis1.2-1.7(%)
Specific Rotation [a]20/D(c=0.2 in MeOH)-155--145(°)
Carbon by Elemental Analysis66.5-67.5(%)
Appearance(S293790)White to Yellow Powder
Proton NMR spectrumConforms to Structure
Solubility in CHCL3,Colorless to Pale Yellow to Yellow,Clear,4.90-5.10 mg/mlPass

Citations of This Product

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39. Huang Yue, Li Jinli, Pei Shifeng, You Heng, Liu Huimin, Guo Yaqiong, Xu Rui, Li Na, Feng Yaoyu, Xiao Lihua.  (2024)  Optimization of a DiCre recombinase system with reduced leakage for conditional genome editing of Cryptosporidium.  Parasites & Vectors,  17  (1): (1-10).  [PMID:39169430] [10.1186/s13071-024-06431-1]
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